Job Title: Project Manager ConsultantJob DescriptionThis is a technical consulting role requiring deep masonry and concrete expertise, strong client interaction, and high-volume onsite assessments.Responsibilities<ul><li>Conduct on-site client visits to assess project needs and scope details.</li><li>Gather all necessary information to prepare precise and competitive bids, including materials identification and pricing.</li><li>Build and maintain strong relationships with clients, partner vendors, and industry professionals such as landscape designers, architects, engineers, and irrigation specialists.</li><li>Prepare and submit detailed bids according to established pricing formulas.</li><li>Develop and execute strategies to meet and exceed monthly sales goals.</li><li>Provide continuous client support and consultation throughout the pre-sale process.</li><li>Prepare contracts and invoices for approved projects.</li><li>Collaborate with the Project Management team to transition approved bids into the planning and execution phase through weekly meetings.</li></ul>Essential Skills<ul><li>10+ years of in-field masonry and concrete experience (both commercial and residential).</li><li>Proven record of success in customer service and sales.</li><li>Strong understanding of masonry and concrete systems, including block, brick, stone, stucco, concrete, tile, grading, machine work, precast, repainting, drainage, waterproofing, and blueprint reading.</li><li>Excellent organizational and communication skills.</li><li>Proficient in computer applications and digital tools.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience in project management and sales within the construction industry.</li></ul>Work EnvironmentThe position is hybrid, allowing for remote work with occasional use of a small office space. The consultant will start from home each day and visit 6-10 sites per day, with a company vehicle assigned for transportation. The standard shift is from 7 AM to 4 PM, but may vary depending on appointments.Job Type &amp; LocationThis is a Permanent position based out of Los Angeles, CA.Pay and BenefitsThe pay range for this position is $85000.00 - $100000.00/yr.Competitive salary up to $85,000 per year
● 2% commission on all closed projects
● Company vehicle and gas card
● Medical insurance
● Professional development assistanceWorkplace TypeThis is a hybrid position in Los Angeles,CA.Application DeadlineThis position is anticipated to close on Feb 28, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

public

Project Manager Consultant

DescriptionJob description:The Scientific Project Manager, QuIL will be responsible for the effective management of data-driven and analytics projects within QuIL, an agile, projectized organization. This role involves working closely with the Chief of Staff for QM&amp;G and the Head of QuIL to implement the operating model, support resource planning, coordinate workshop logistics, and lead sprint management activities. The project manager will ensure stakeholders have transparent access to project and sprint status by establishing the right tools and processes.Key responsibilities include:• Coordinating project activities and timelines across multiple concurrent data science projects and sprints.• Facilitating team communication and fostering collaboration between QuIL scientists, visiting scientists and cross-functional partners.• Organizing and supporting logistics for agile sprints, workshops, and resource planning sessions.• Implementing tools and processes for tracking sprint progress, managing deliverables, and facilitating knowledge transfer within the team.• Proactively identifying and driving operational efficiencies to optimize the QuIL team's effectiveness.The ideal candidate will have a strong background in project management within technical or data science domains and experience managing complex projects with multiple stakeholders. Excellent communication and organizational skills are required. Familiarity with agile methodologies, data science, analytics, or related technical fields is desirable but not necessary. Experience with implementing project management tools and continuous improvement practices is a plus. Relevant project management certifications or a technical degree at the bachelor's or higher level are advantageous. This is an individual contributor role requiring the ability to work cross-functionally in a dynamic and iterative environment.Additional Skills &amp; QualificationsRequired Experience, Education &amp; Certifications•	3–5 years of experience (more is acceptable)•	Agile experience in a scientific or technical environment strongly preferred•	Education: Master’s degree is acceptable; PhD may be considered overqualified•	Certifications: Not required•	PMP is not heavily weighted compared to hands on experience________________________________________Nice-to-Have Qualifications•	PMP certification or equivalent PM credential•	Stronger technical/scientific domain expertise•	Experience supporting data science projects, analytics workflows, or technical R&amp;D teams•	experience in quantitative fields (DS, CS, statistics, math, engineering)•	Experience with Smartsheet, Teams, SharePoint, and similar platforms________________________________________Remote / Onsite Expectations•	Primarily onsite in Lake County •	Hybrid flexibility: 1–2 days remote•	Expected onsite: Tues–Thurs requiredExperience LevelIntermediate LevelJob Type &amp; LocationThis is a Contract position based out of North Chicago, IL.Pay and BenefitsThe pay range for this position is $65.00 - $70.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in North Chicago,IL.Application DeadlineThis position is anticipated to close on Feb 20, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Project Manager II (Non-IT)

Job Title: Project ManagerJob DescriptionWe are seeking a highly organized and proactive Project Manager to support the Discovery and Translational Development (DTD) group. This role involves developing and executing translational strategies that enable Investigational New Drug (IND) applications for our pipeline programs. The Project Manager will collaborate closely with the Head of DTD, DTD group members, and cross-functional teams to plan, track, and coordinate scientific and operational activities that drive our early-stage programs toward clinical development.Responsibilities<ul><li>Partner with DTD leadership and functionality leads to build and maintain detailed project timelines across multiple programs.</li><li>Coordinate cross-functional activities supporting IND-enabling efforts, including preclinical studies, assay development, biomarker discovery, and translational research.</li><li>Track key milestones, deliverables, risks, and dependencies; flag potential delays and help drive mitigation plans.</li><li>Prepare and facilitate team meetings, ensuring clear agendas, minutes, and follow-ups.</li><li>Support planning and execution of stage-gate reviews, decision-making forums, and development strategy updates.</li><li>Maintain centralized documentation and communication channels to ensure team alignment and knowledge sharing.</li><li>Work closely with other project managers, program managers, and functional teams across Research, Regulatory, CMC, and Clinical Development.</li><li>Contribute to process improvements and operational best practices within the DTD group.</li></ul>Essential Skills<ul><li>Bachelor’s degree in a scientific discipline required; advanced degree (MS, PhD) or PMP certification is a plus.</li><li>Project management experience in a biotech/pharmaceutical R&amp;D setting is preferable; experience supporting translational/preclinical or early development teams is highly desirable.</li><li>Strong understanding of drug development timelines, particularly IND-enabling activities.</li></ul>Additional Skills &amp; Qualifications<ul><li>Excellent organizational, interpersonal, and communication skills.</li><li>Demonstrated ability to manage multiple priorities, work collaboratively, and maintain attention to detail.</li><li>Proficiency with project management tools (e.g., MS Project, Smartsheet, Wrike, or similar).</li></ul>Work EnvironmentThis role is hybrid, ideally 2 days a week onsite, aligning with our mission to improve the daily lives of patients living with devastating rare diseases.Job Type &amp; LocationThis is a Contract position based out of Boston, MA.Pay and BenefitsThe pay range for this position is $75.00 - $82.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a hybrid position in Boston,MA.Application DeadlineThis position is anticipated to close on Feb 23, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Project Manager- Discovery And Translational Development

DescriptionThis company in Medina, Ohio is seeking a 2-4 year Project Manager/Estimator to handle project oversight from initial bid through completion, including preparing accurate estimates, developing proposals, coordinating subcontractors and suppliers, managing schedules and budgets, conducting site visits, maintaining documentation, and ensuring high‑quality workmanship and strong client communication. eIdeal candidates would have an engineering or constructio experience with 2-4 years of project management or estimating experience. Most of their projects are in the Water/Wastewater industry. They would also consider someone who has started in the trades as well. Their project range from $5 to $10 million in size. This is a salary role.SkillsEstimation, Project management, Construction, Bidding, Rfi, submittalsTop Skills DetailsEstimation,Project management,ConstructionAdditional Skills &amp; QualificationsMust Haves:-2-4 years of PM experience- Construction experience- MS Projects, Procore, or BluebeamNice to Haves:- Engineering- Water/Wastewater experienceExperience LevelEntry LevelJob Type &amp; LocationThis is a Contract position based out of Medina, OH.Pay and BenefitsThe pay range for this position is $43.27 - $52.88/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Medina,OH.Application DeadlineThis position is anticipated to close on Mar 5, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Project Manager/estimator

Job Title: Project MonitorJob DescriptionThe Project Monitor is responsible for on-site oversight of asbestos abatement projects, ensuring compliance with all federal, state, and local regulations. This role plays a crucial part in supporting public health and safety by monitoring abatement activities, performing air sampling, and documenting project compliance throughout the duration of the work.Responsibilities<ul><li>Provide on-site oversight of asbestos abatement projects.</li><li>Ensure compliance with all applicable federal, state, and local regulations.</li><li>Monitor abatement activities to support public health and safety.</li><li>Perform air sampling to assess environmental safety.</li><li>Document project compliance throughout the duration of the work.</li><li>Complete field documentation independently.</li><li>Collect air samples as part of project compliance monitoring.</li></ul>Essential Skills<ul><li>Experience with asbestos inspection and hazardous material handling.</li><li>Comfortable working in the field, especially in buildings.</li><li>Valid NYS driver’s license and access to a vehicle.</li><li>Knowledge of asbestos regulations, including NYSDOL Industrial Code Rule 56.</li><li>Asbestos certificate and understanding of EPA regulations.</li><li>Proficiency in construction management.</li><li>OSHA 40-hour HAZWOPER certification.</li></ul>Additional Skills &amp; Qualifications<ul><li>NYSDOL Asbestos Project Monitor certification or willingness to obtain through paid training.</li><li>EPA Lead certification.</li><li>Experience with asbestos air sampling and project monitoring is preferred.</li></ul>Work EnvironmentThe role involves working in the field, primarily in buildings, with occasional weekday and weekend availability required. Employees enjoy a family-like culture and opportunities for certification. The position does not require physical contact with asbestos.Job Type &amp; LocationThis is a Contract to Hire position based out of Buffalo, NY.Pay and BenefitsThe pay range for this position is $19.00 - $25.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Buffalo,NY.Application DeadlineThis position is anticipated to close on Feb 26, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Project Monitor

Job Title: Project MonitorJob DescriptionThe Project Monitor is responsible for on-site oversight of asbestos abatement projects, ensuring compliance with all federal, state, and local regulations. This role plays a crucial part in supporting public health and safety by monitoring abatement activities, performing air sampling, and documenting project compliance throughout the duration of the work.Responsibilities<ul><li>Provide on-site oversight of asbestos abatement projects.</li><li>Ensure compliance with all applicable federal, state, and local regulations.</li><li>Monitor abatement activities to support public health and safety.</li><li>Perform air sampling to assess environmental safety.</li><li>Document project compliance throughout the duration of the work.</li><li>Complete field documentation independently.</li><li>Collect air samples as part of project compliance monitoring.</li></ul>Essential Skills<ul><li>Experience with asbestos inspection and hazardous material handling.</li><li>Comfortable working in the field, especially in buildings.</li><li>Valid NYS driver’s license and access to a vehicle.</li><li>Knowledge of asbestos regulations, including NYSDOL Industrial Code Rule 56.</li><li>Asbestos certificate and understanding of EPA regulations.</li><li>Proficiency in construction management.</li><li>OSHA 40-hour HAZWOPER certification.</li></ul>Additional Skills &amp; Qualifications<ul><li>NYSDOL Asbestos Project Monitor certification or willingness to obtain through paid training.</li><li>EPA Lead certification.</li><li>Experience with asbestos air sampling and project monitoring is preferred.</li></ul>Work EnvironmentThe role involves working in the field, primarily in buildings, with occasional weekday and weekend availability required. Employees enjoy a family-like culture and opportunities for certification. The position does not require physical contact with asbestos.Job Type &amp; LocationThis is a Contract to Hire position based out of Buffalo, NY.Pay and BenefitsThe pay range for this position is $19.00 - $25.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Buffalo,NY.Application DeadlineThis position is anticipated to close on Feb 27, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Job Title: Project SchedulerJob DescriptionEnhance your proficiency in schedule development and analysis, integrated cost and schedule forecasting using quantitative risk management tools and techniques. These include Expected Monetary Value and Sensitivity Analysis to better predict project schedule and cost performance, enabling timely corrective, preventive, and predictive actions. Apply integrated objective risk management to project baselines to optimize project risk responses, and review and coordinate the management and utilization of project management guidelines, standards, processes, job aids, and tools. Integrate all project management subsidiary systems to improve project performance, providing continuous lifecycle planning and scheduling processes with progressive risk management forecasting. Manage the project schedule performance baseline and forecast schedule performance, identifying opportunities to avoid negative variances. Perform standard and advanced project and special project schedule reporting for stakeholders, compiling and producing schedule reports as needed. Utilize communication competence to drive effective project schedule decision-making.Responsibilities<ul><li>Increase proficiency in schedule development and analysis using quantitative risk management tools.</li><li>Apply integrated risk management to optimize project risk responses.</li><li>Review and coordinate project management guidelines and tools.</li><li>Integrate project management subsidiary systems to improve performance.</li><li>Provide continuous lifecycle planning with progressive risk management forecasting.</li><li>Manage project schedule performance baseline and integrated project baselines.</li><li>Forecast schedule performance and identify opportunities to avoid negative variances.</li><li>Perform standard and advanced project schedule reporting for stakeholders.</li><li>Utilize communication competence to facilitate effective decision-making.</li></ul>Essential Skills<ul><li>High degree of proficiency in scheduling software (P6) and spreadsheet development.</li><li>Integrated knowledge base in project scope-schedule-cost, risk-quality management.</li><li>High School diploma and four years of experience working as a scheduler, or High School diploma and six years of construction/engineering experience with two years as a project scheduler, or Bachelor’s Degree and four years’ experience as a project scheduler.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor’s Degree and four years’ experience as a project scheduler preferred.</li><li>Ability to read and interpret schedules and proficiency in P6 and database development.</li><li>Experience in large industrial Capital Project environments.</li></ul>Work EnvironmentThis role begins with in-office training for the first few weeks, transitioning to a hybrid model where you will work in the office on Tuesdays, Wednesdays, and Thursdays. You will have opportunities to work on diverse projects in electric and natural gas systems and infrastructure upgrades, and be exposed to cutting-edge technologies and compliance systems, fostering continuous learning.Job Type &amp; LocationThis is a Contract to Hire position based out of Valparaiso, IN.Pay and BenefitsThe pay range for this position is $60.00 - $70.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a hybrid position in Valparaiso,IN.Application DeadlineThis position is anticipated to close on Feb 28, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Project Scheduler

Job Title: Project SchedulerJob DescriptionWe are seeking a skilled Project Scheduler with a strong background in coordinating, scheduling, and identifying project milestones for long-term, mid-term, and near-term initiatives. The ideal candidate will effectively manage scheduling and coordination issues, utilizing MS Project to consolidate schedules across multiple projects. This role requires defining goals, objectives, deliverables, and associated timelines to ensure project success.Responsibilities<ul><li>Coordinate and schedule project/program milestones and related activities across long-term, mid-term, and near-term timelines.</li><li>Identify and address scheduling and coordination issues to ensure project alignment.</li><li>Utilize MS Project to consolidate multiple project schedules, ensuring seamless integration and management.</li><li>Define project goals, objectives, deliverables, and timelines to meet program requirements.</li></ul>Essential Skills<ul><li>Proficiency in project coordination and scheduling.</li><li>Experience with MS Project.</li><li>Ability to manage multiple projects simultaneously.</li><li>Strong problem-solving skills to address scheduling and coordination issues.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience in the aerospace sector.</li></ul>Work EnvironmentThe position is based in an office/manufacturing environment, providing opportunities to engage with cutting-edge aerospace technologies. The work setting supports collaborative efforts in a dynamic and innovative industry.Job Type &amp; LocationThis is a Contract to Hire position based out of Louisville, CO.Pay and BenefitsThe pay range for this position is $50.00 - $60.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Louisville,CO.Application DeadlineThis position is anticipated to close on Feb 23, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Job Title: Project SchedulerJob DescriptionWe are seeking a skilled Project Scheduler with a strong background in coordinating, scheduling, and identifying project milestones for long-term, mid-term, and near-term initiatives. The ideal candidate will effectively manage scheduling and coordination issues, utilizing MS Project to consolidate schedules across multiple projects. This role requires defining goals, objectives, deliverables, and associated timelines to ensure project success.Responsibilities<ul><li>Coordinate and schedule project/program milestones and related activities across long-term, mid-term, and near-term timelines.</li><li>Identify and address scheduling and coordination issues to ensure project alignment.</li><li>Utilize MS Project to consolidate multiple project schedules, ensuring seamless integration and management.</li><li>Define project goals, objectives, deliverables, and timelines to meet program requirements.</li></ul>Essential Skills<ul><li>Proficiency in project coordination and scheduling.</li><li>Experience with MS Project.</li><li>Ability to manage multiple projects simultaneously.</li><li>Strong problem-solving skills to address scheduling and coordination issues.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience in the aerospace sector.</li></ul>Work EnvironmentThe position is based in an office/manufacturing environment, providing opportunities to engage with cutting-edge aerospace technologies. The work setting supports collaborative efforts in a dynamic and innovative industry.Job Type &amp; LocationThis is a Contract to Hire position based out of Louisville, CO.Pay and BenefitsThe pay range for this position is $50.00 - $60.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Louisville,CO.Application DeadlineThis position is anticipated to close on Feb 20, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Job Title: Program SchedulerJob DescriptionWe are seeking a skilled Program Scheduler with a strong background in coordinating, scheduling, and identifying project milestones for long-term, mid-term, and near-term initiatives. The ideal candidate will effectively manage scheduling and coordination issues, utilizing MS Project to consolidate schedules across multiple projects. This role requires defining goals, objectives, deliverables, and associated timelines to ensure project success.Responsibilities<ul><li>Coordinate and schedule project/program milestones and related activities across long-term, mid-term, and near-term timelines.</li><li>Identify and address scheduling and coordination issues to ensure project alignment.</li><li>Utilize MS Project to consolidate multiple project schedules, ensuring seamless integration and management.</li><li>Define project goals, objectives, deliverables, and timelines to meet program requirements.</li></ul>Essential Skills<ul><li>Proficiency in project coordination and scheduling.</li><li>Experience with MS Project.</li><li>Ability to manage multiple projects simultaneously.</li><li>Strong problem-solving skills to address scheduling and coordination issues.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience in the aerospace sector.</li></ul>Work EnvironmentThe position is based in an office/manufacturing environment, providing opportunities to engage with cutting-edge aerospace technologies. The work setting supports collaborative efforts in a dynamic and innovative industry.Job Type &amp; LocationThis is a Contract to Hire position based out of Louisville, CO.Pay and BenefitsThe pay range for this position is $50.00 - $75.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Louisville,CO.Application DeadlineThis position is anticipated to close on Feb 26, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Job Title: Program SchedulerJob DescriptionWe are seeking a skilled Program Scheduler with a strong background in coordinating, scheduling, and identifying project milestones for long-term, mid-term, and near-term initiatives. The ideal candidate will effectively manage scheduling and coordination issues, utilizing MS Project to consolidate schedules across multiple projects. This role requires defining goals, objectives, deliverables, and associated timelines to ensure project success.Responsibilities<ul><li>Coordinate and schedule project/program milestones and related activities across long-term, mid-term, and near-term timelines.</li><li>Identify and address scheduling and coordination issues to ensure project alignment.</li><li>Utilize MS Project to consolidate multiple project schedules, ensuring seamless integration and management.</li><li>Define project goals, objectives, deliverables, and timelines to meet program requirements.</li></ul>Essential Skills<ul><li>Proficiency in project coordination and scheduling.</li><li>Experience with MS Project.</li><li>Ability to manage multiple projects simultaneously.</li><li>Strong problem-solving skills to address scheduling and coordination issues.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience in the aerospace sector.</li></ul>Work EnvironmentThe position is based in an office/manufacturing environment, providing opportunities to engage with cutting-edge aerospace technologies. The work setting supports collaborative efforts in a dynamic and innovative industry.Job Type &amp; LocationThis is a Contract to Hire position based out of Louisville, CO.Pay and BenefitsThe pay range for this position is $50.00 - $75.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Louisville,CO.Application DeadlineThis position is anticipated to close on Feb 27, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Job Title: Project SchedulerJob DescriptionEnhance your proficiency in schedule development and analysis, integrated cost and schedule forecasting using quantitative risk management tools and techniques. These include Expected Monetary Value and Sensitivity Analysis to better predict project schedule and cost performance, enabling timely corrective, preventive, and predictive actions. Apply integrated objective risk management to project baselines to optimize project risk responses, and review and coordinate the management and utilization of project management guidelines, standards, processes, job aids, and tools. Integrate all project management subsidiary systems to improve project performance, providing continuous lifecycle planning and scheduling processes with progressive risk management forecasting. Manage the project schedule performance baseline and forecast schedule performance, identifying opportunities to avoid negative variances. Perform standard and advanced project and special project schedule reporting for stakeholders, compiling and producing schedule reports as needed. Utilize communication competence to drive effective project schedule decision-making.Responsibilities<ul><li>Increase proficiency in schedule development and analysis using quantitative risk management tools.</li><li>Apply integrated risk management to optimize project risk responses.</li><li>Review and coordinate project management guidelines and tools.</li><li>Integrate project management subsidiary systems to improve performance.</li><li>Provide continuous lifecycle planning with progressive risk management forecasting.</li><li>Manage project schedule performance baseline and integrated project baselines.</li><li>Forecast schedule performance and identify opportunities to avoid negative variances.</li><li>Perform standard and advanced project schedule reporting for stakeholders.</li><li>Utilize communication competence to facilitate effective decision-making.</li></ul>Essential Skills<ul><li>High degree of proficiency in scheduling software (P6) and spreadsheet development.</li><li>Integrated knowledge base in project scope-schedule-cost, risk-quality management.</li><li>High School diploma and four years of experience working as a scheduler, or High School diploma and six years of construction/engineering experience with two years as a project scheduler, or Bachelor’s Degree and four years’ experience as a project scheduler.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor’s Degree and four years’ experience as a project scheduler preferred.</li><li>Ability to read and interpret schedules and proficiency in P6 and database development.</li><li>Experience in large industrial Capital Project environments.</li></ul>Work EnvironmentThis role begins with in-office training for the first few weeks, transitioning to a hybrid model where you will work in the office on Tuesdays, Wednesdays, and Thursdays. You will have opportunities to work on diverse projects in electric and natural gas systems and infrastructure upgrades, and be exposed to cutting-edge technologies and compliance systems, fostering continuous learning.Job Type &amp; LocationThis is a Contract to Hire position based out of Valparaiso, IN.Pay and BenefitsThe pay range for this position is $60.00 - $70.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a hybrid position in Valparaiso,IN.Application DeadlineThis position is anticipated to close on Mar 3, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Job Title: SurveyorJob DescriptionWe are seeking a highly skilled Surveyor with 7-10 years of experience to support solar and wind farm projects. The ideal candidate will have experience in power and utility projects, although this is not a strict requirement. The role involves coordinating field crew activities, ensuring data accuracy, and assisting with budgeting and project schedules.Responsibilities<ul><li>Coordinate daily activities of at least one field crew and/or survey technician.</li><li>Analyze and review work of survey crews to verify data accuracy at survey sites.</li><li>Assist project managers with budgeting, project cost control, and meeting project schedules.</li><li>Process and file survey data files, field notes, photos, and sketches.</li><li>Perform CAD work to create and finalize survey drawings.</li><li>Use Excel and survey programs to process and verify data, and run reports.</li><li>Perform daily downloads of data collector files.</li><li>Research deeds and maps, perform boundary analysis, and make determinations.</li><li>Calculate heights, depths, relative positions, property lines, and terrain characteristics.</li><li>Prepare all data, charts, plots, maps, records, and documents related to surveys.</li><li>Perform calculations and interpret design plans for construction staking.</li><li>Prepare cut sheets for field crews and write legal descriptions.</li><li>Maintain exceptional internal and external client relations.</li><li>All other duties as assigned.</li></ul>Essential Skills<ul><li>Bachelor’s degree in Land Surveying or equivalent education and experience.</li><li>CST level two or equivalent education and experience required.</li><li>Minimum four years of applicable experience.</li><li>Proficiency in AutoCAD and MicroStation.</li><li>Experience with field to finish procedures, ALTA/NSPS Land Title Standards, and GPS data processing.</li><li>Ability to create and analyze legal descriptions.</li><li>Valid driver’s license and ability to travel to corporate offices and project sites.</li><li>Exceptional written, presentation, and interpersonal communication skills.</li><li>Ability to work efficiently under tight deadlines and balance multiple projects.</li></ul>Additional Skills &amp; Qualifications<ul><li>SIT or PS license preferred.</li><li>Field experience as a Chief Field Surveyor is a plus.</li><li>Experience with project management, budgeting, and cost control.</li><li>Resourceful, action-oriented, creative, and analytical thinker.</li><li>Strong planning, organization, preparation, and execution capabilities.</li><li>Open to new ideas, innovation, and change.</li><li>Strong problem-solving and analytical skills.</li></ul>Work EnvironmentThis position primarily operates in an office environment with occasional site visits. The typical workweek is 40-50 hours. The team consists of 8 field crews and 7 office staff. The work culture values dynamic, daring, and diverse problem-solving approaches, focusing on client-centric solutions and community goals.Job Type &amp; LocationThis is a Contract to Hire position based out of Plymouth, MI.Pay and BenefitsThe pay range for this position is $33.65 - $38.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Plymouth,MI.Application DeadlineThis position is anticipated to close on Feb 27, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Project Surveyor

<h1>Project Technician</h1><h2>Position Overview</h2>We are seeking an experienced Project Technician to support and coordinate a wide range of industrial and facility‑related projects. This role involves work across electrical and plumbing systems, operations and maintenance (O&amp;M), decontamination, demolition, and general facility operations. The position requires strong coordination skills, a focus on safety, and the ability to ensure projects are completed efficiently and in line with client expectations.<h2>Key Responsibilities</h2><ul><li>Staff coordination and scheduling, including oversight of direct reports</li><li>Manage day‑to‑day project activities, including ordering equipment and materials</li><li>Coordinate subcontractors and develop detailed work plans</li><li>Ensure safety compliance through proper documentation, procedures, and equipment</li><li>Serve as a client liaison to maintain standards and identify additional support needs</li><li>Maintain accurate project documentation and support overall workflow</li></ul><h2>Essential Skills</h2><ul><li>10+ years of project coordination experience</li><li>MEP, water/wastewater, facility operations, or machine guarding</li><li>Strong leadership and mentoring abilities</li><li>Comfortable in client‑facing communication</li><li>Expertise in material coordination, subcontractor oversight, and logistics</li><li>Strong organizational and project management skills</li><li>Experience in facility or facility‑management environments</li></ul><h2>Additional Qualifications</h2><ul><li>College degree preferred but not required</li><li>High attention to detail and ability to manage multiple priorities</li><li>Willingness to travel as needed for project support</li></ul>Job Type &amp; LocationThis is a Contract position based out of Plainville, CT.Pay and BenefitsThe pay range for this position is $38.46 - $43.25/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Plainville,CT.Application DeadlineThis position is anticipated to close on Feb 24, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Project Technician

Job Title: Project/Program ManagerJob DescriptionResponsible for the coordination and completion of projects or programs, overseeing all aspects from inception to completion. This role involves setting deadlines, assigning responsibilities, and monitoring the progress of projects. The Project/Program Manager will prepare reports for upper management regarding the status of projects and programs. A bachelor's degree and at least 7 years of experience in the field or a related area are required. The role requires familiarity with a variety of concepts, practices, and procedures within the field. Extensive experience and judgment are relied upon to plan and accomplish goals, with a wide degree of creativity and latitude expected.Responsibilities<ul><li>Lead pilot site selection, alignment, and launch support activities with site TOM teams.</li><li>Coordinate vendor relationships and manage external partner deliverables.</li><li>Drive SOP documentation, training development, and rollout execution for ROC and field operations.</li><li>Establish success metrics, track pilot performance, and provide scale viability recommendations.</li><li>Triage and close-loop on technical bugs with engineering teams.</li><li>Manage PMO approvals and compliance requirements across programs.</li><li>Track deployment milestones, identify blockers, and drive resolution.</li><li>Support workflow adoption, error-handling processes, and continuous improvement initiatives.</li><li>Identify and manage program dependencies across technology, operations, and business teams.</li><li>Proactively surface risks and develop mitigation strategies.</li><li>Build contingency plans and drive issue resolution with appropriate urgency.</li><li>Ensure alignment on timelines, resources, and delivery commitments.</li></ul>Essential Skills<ul><li>Program management and project management experience.</li><li>MBA or Master's degree.</li><li>PMP, Agile, or Six Sigma certification.</li><li>Experience with automation technologies and IoT deployments.</li><li>Background in security systems or authentication solutions.</li><li>International program management experience.</li><li>Vendor management and external partnerships experience.</li></ul>Additional Skills &amp; Qualifications<ul><li>10+ years of program/project management experience in technology or operations.</li><li>Proven track record managing complex, multi-stakeholder programs with competing priorities.</li><li>Experience with transportation, logistics, or supply chain operations preferred.</li><li>Strong technical acumen with the ability to understand and communicate technical concepts.</li><li>Demonstrated ability to influence without authority across all organizational levels.</li></ul>Work EnvironmentThe work environment involves managing technical software or hardware, particularly in tech or operations, and includes supply chain management. This role typically reports to a manager or head of a unit/department, requiring the ability to lead and direct the work of others.Job Type &amp; LocationThis is a Contract position based out of Bellevue, WA.Pay and BenefitsThe pay range for this position is $65.00 - $68.50/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Bellevue,WA.Application DeadlineThis position is anticipated to close on Mar 6, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Project/Program Manager

Job Title: Construction Project ManagerJob DescriptionWe are seeking a dedicated and experienced Construction Project Manager who will be responsible for the coordination and successful completion of projects and programs. The candidate will oversee all aspects, set deadlines, assign responsibilities, and monitor progress. They will prepare reports for upper management regarding the status of the projects and programs.Responsibilities<ul><li>Coordinate and complete projects and programs efficiently.</li><li>Oversee all aspects of projects/programs, from inception to completion.</li><li>Set deadlines, assign responsibilities, and monitor project/program progress.</li><li>Prepare comprehensive reports for upper management on project/program status.</li><li>Lead and direct the work of team members.</li><li>Utilize creativity and judgment to plan and accomplish project goals.</li><li>Report on-site activities to the blue badge construction manager.</li><li>Collaborate effectively with internal and external stakeholders.</li><li>Manage new builds, renovations, and expansions of Fulfillment Centers across the US.</li></ul>Essential Skills<ul><li>Bachelor’s degree in Architecture, Engineering, Construction Management, or a comparable field.</li><li>At least 7 years of experience in a related discipline such as Architecture, Engineering, or Construction Management.</li><li>7+ years of project management experience from design phase through implementation and operation.</li><li>7+ years of experience in negotiating construction, procurement, and labor contracts.</li><li>Familiarity with AutoCAD, BIM, and scheduling software such as Primavera or MS Project.</li><li>Experience in project coordination and site development.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience in at least two disciplines within the construction industry, including General Contracting, Owner’s Representation, Commercial Development, Engineering &amp; Design, or similar.</li><li>Success in communicating project requirements to various audiences.</li><li>Experience in facilities management or similar roles, including planning, design review, implementation, and project management/control of new structures and existing buildings.</li><li>Program management of concurrent projects.</li><li>Project Management accreditation (PMP® or similar).</li></ul>Work EnvironmentThis position requires someone to be onsite in Tremont, PA 3 days a week.Job Type &amp; LocationThis is a Contract position based out of Tremont, PA.Pay and BenefitsThe pay range for this position is $50.00 - $55.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a hybrid position in Tremont,PA.Application DeadlineThis position is anticipated to close on Mar 6, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Project/Program Manager III

Job Title: Propulsion Test Stand EngineerJob DescriptionWe are seeking highly driven, hands-on Systems &amp; Fluid Design Engineers to support multiple high-urgency test-stand infrastructure and fluid system projects. This work includes designing, modifying, building, and commissioning high-pressure and cryogenic gas systems used in rocket engine development and test environments. The role is ideal for engineers who thrive in fast-paced, unpredictable environments and who enjoy both conceptual design and real-world activation of the hardware they build. You will partner directly with lead engineers and technicians to execute end-to-end system ownership—design through commissioning—and help solve real-time challenges that arise during testing and operations.Responsibilities<ul><li>Design new or updated high-pressure and cryogenic fluid, gas, and piping systems (e.g., LN2, LOX, high-pressure helium, nitrogen systems).</li><li>Create system-level CAD models and drawings using NX Unigraphics (SolidWorks/Creo/Catia transferable).</li><li>Perform structural and thermal analysis using ANSYS or similar tools.</li><li>Select and integrate commercial off-the-shelf components and specify custom fabricated tubing/piping.</li><li>Act as the de facto project manager for system builds.</li><li>Coordinate with technicians, welders, fabricators, and trades to efficiently execute construction.</li><li>Oversee installation, testing, troubleshooting, and final activation of systems, solving day-of issues.</li><li>Ensure systems are handed off fully tested, commissioned, and ready for operations.</li><li>Work alongside lead engineers, operations personnel, and other system owners.</li><li>Communicate clearly with both engineering and hands-on personnel.</li><li>Navigate a fast-paced culture, prioritize multiple active projects, and act with urgency.</li></ul>Essential Skills<ul><li>Bachelor's in Engineering.</li><li>1+ years of experience with liquid and gas pumps, high-pressure gas systems, cryogenic systems, valves, and instrumentation.</li><li>3+ years of design experience in an industrial setting.</li><li>3+ years of project management experience, including managing deadlines, costs, and coordinating with tradespeople.</li><li>Experience with ANSYS and NX Unigraphics (or similar design software).</li><li>Ability to provide demonstrated examples of success navigating the design, build, and activation phases.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience in A&amp;D, chemical refinery plants, air separation units, cryogenic systems, oil and gas industries.</li><li>Comfortable with getting hands dirty and overcoming unexpected obstacles quickly.</li><li>Experience in developing, commissioning, and reducing downtime.</li><li>Ownership of the lifecycle from design to build to activation in a plant or R&amp;D environment.</li></ul>Work EnvironmentThe position is based at the McGregor site with a flexible shift schedule roughly from 8 AM to 6 PM. The baseline workweek is 5 days, with the possibility of extending to 6 days if required. The work environment is dynamic, requiring quick adaptation and collaboration with various team members to ensure successful project completion.Job Type &amp; LocationThis is a Contract position based out of Mcgregor, TX.Pay and BenefitsThe pay range for this position is $40.00 - $70.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Mcgregor,TX.Application DeadlineThis position is anticipated to close on Mar 1, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Propulsion Test Stand Engineer

Sr Protection and Control EngineerResponsibilities<ul><li>Develop project scopes, one-line diagrams, and estimates for substation projects.</li><li>Review substation construction drawings, including electrical arrangements, plan and section views, grounding, cable and conduit drawings, ensuring compliance with codes and standards.</li><li>Engineer and design lightning protection, grounding, and equipment replacement and repair for substations.</li><li>Make changes and corrections to drawings and documentation as necessary.</li><li>Verify the proper use of equipment and material according to project documentation standards and codes.</li><li>Ensure timely ordering and delivery of material and equipment for substation construction.</li><li>Travel to project sites for walk downs and gather information to develop accurate requirements for substation projects.</li><li>Lead substation projects and coordinate work activities within the department.</li><li>Provide training and guidance to lower-level employees.</li><li>Initiate corrective action when substation project objectives are not being met.</li></ul>Essential Skills<ul><li>Five to eight years of experience in utilities working with protection and controls.</li><li>Five to eight years of experience completing engineering projects from start to finish.</li><li>Bachelor’s Degree in Electrical Engineering</li><li>Proficiency in substation design, AutoCAD, and electrical drafting.</li><li>A PE License is desirable but not required.</li></ul>Job Type &amp; LocationThis is a Permanent position based out of Columbus, OH.Pay and BenefitsThe pay range for this position is $35.00 - $45.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully remote position.Application DeadlineThis position is anticipated to close on Mar 2, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Protection And Control Engineer

Job Title: Protection and Control EngineerJob DescriptionThe primary responsibility of this position will be to support the development of protective relay settings for distribution feeder breakers within transmission substations. Our team requires a dedicated engineering resource to manage the increasing requests for relay settings changes due to the substantial capital investment in our distribution system.Responsibilities<ul><li>Verify and update distribution substation short circuit models using CAPE.</li><li>Populate calculation sheets and solicit feedback from the Distribution engineering team.</li><li>Perform time overcurrent coordination studies of distribution substation power transformers and breakers.</li><li>Review distribution substation protective relay logic and control drawings.</li></ul>Essential Skills<ul><li>Bachelor’s degree in Engineering or Engineering Technology, preferably with an electrical emphasis.</li><li>Experience in performing protective relay calculations and coordination studies.</li><li>Proficiency in using power system simulation software such as CAPE, CYME, ASPEN, EDSA, or ETAP.</li><li>Knowledge of substation protective relay testing and control scheme testing.</li><li>Understanding of transmission and/or distribution substation operations.</li></ul>Additional Skills &amp; Qualifications<ul><li>Courses in Power System Analysis, Protective Relaying, Control Systems, Electric Machine Theory, and Symmetrical Components are beneficial.</li></ul>Work EnvironmentThis position offers a hybrid work environment in a cubicle setting, where team collaboration is emphasized. The role is full-time and functions as an integral part of the engineering consultant team.Job Type &amp; LocationThis is a Contract to Hire position based out of Forest Park, GA.Pay and BenefitsThe pay range for this position is $39.00 - $45.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a hybrid position in Forest Park,GA.Application DeadlineThis position is anticipated to close on Feb 27, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Job Title: Protection and Control EngineerJob DescriptionThe Staff Electrical Engineer will be responsible for performing protection and control design on various substation projects. This role involves collaborating with the project team throughout the design and construction phases, ensuring that protection and control plans align with budget limitations, design requirements, and client needs. Preference is given to candidates with experience in protection and control design.Responsibilities<ul><li>Perform protection and control design for substation projects.</li><li>Collaborate with the project team during design and construction phases.</li><li>Adjust protection and control plans to meet budget limitations, design requirements, and client needs.</li></ul>Essential Skills<ul><li>Degree in Electrical Engineering (ABET Accredited).</li><li>3-6 years of experience in protection &amp; controls design for substations.</li><li>Experience with high voltage (35kv or greater, transmission level experience is key).</li><li>Experience with AutoCAD Electrical.</li><li>Professional Engineer (PE) or Engineer in Training (EIT) certification.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience working within AutoCAD Electrical.</li><li>Beneficial to have data center experience.</li></ul>Work EnvironmentThe position involves working mainly in the office with approximately 10% travel to sites. The role offers benefits such as an ESOP Program and a large bonus structure. Direct hire options are available if needed.Job Type &amp; LocationThis is a Contract to Hire position based out of Alpharetta, GA.Pay and BenefitsThe pay range for this position is $105000.00 - $170000.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Alpharetta,GA.Application DeadlineThis position is anticipated to close on Feb 24, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Position SummaryActalent Services, LLC connects passion with purpose. We are supporting critical engineering and sciences initiatives that advance how companies serve the world. With almost 40 years of experience, our scalable talent solutions and engineering and sciences services provide the expertise our customers need to achieve more.The position falls within the Protection and Controls Department of the organization. The engineer will complete protection and control projects that support our customer. They will work with in-house and client engineers and designers. They will provide, coordinate, and conduct training to lower level engineers.Primary Duties and Responsibilities<ul><li>Work on green-field and brown-field (retrofit) Protection and Control Projects in substations</li><li>Set relays and conduct relay setting calculations utilizing ASPEN, AcSELerator 5010 (SEL), and GE URPC Software</li><li>Design settings in appropriate format then issue to assigned Protection and Controls Supervisor using IPS</li><li>Mark-up and review protection schematics and elementaries</li><li>Utilize MOB Port to review equipment and materials established by substation engineers for Protection Designers</li><li>Work with the following equipment: transformers, circuit breakers, buses, reactors, line disconnects, protective relays systems (SEL, ABB, etc.), and SCADA systems</li><li>Function as a project lead for protection and control projects</li><li>Perform all engineering and design activities with minimum direction</li><li>Lead, facilitate, and coordinate work activities of others within the work group, team, department, or those external to complete substation projects</li><li>Provide training and guidance to lower level employees</li><li>Identify and initiate corrective action when substation project objectives are not being met</li><li>Interpret codes and regulations and develop standards for construction projects</li><li>Promote engineering professionalism and standards</li><li>Develop, recommend, and implement plans by establishing goals, objectives, and requirements that include all scheduling, resources, and cont information for complex engineering</li><li>Position requires 10-15% travel to field substations</li></ul>Education and Experience Requirements<ul><li>Five to eight years of experience in utilities working with protection and controls</li><li>Five to eight years of experience completing engineering projects from start to finish</li><li>Five to eight years of experience setting relays and designing one line diagrams</li><li>Bachelor’s Degree in Electrical Engineering (ABET)</li><li>Master’s Degree in Electrical Engineering (ABET) will count toward years’ experience</li><li>A PE License is required</li></ul>Requisite Abilities and Skills<ul><li>Intermediate ability to perform design calculations such as battery sizing, AC and DC loads, system component selection, power transformer and circuit breaker selection, circuit protection, control and power cable selection and rating, bus bars, fittings, insulators, ground grid design, and lightning protection</li><li>Intermediate understanding of standards and codes such as IEEE, ANSI, NERC-PRC, NEC, and NESC</li><li>Possess intermediate understanding of protection and control equipment, relays, and fault analysis</li><li>Strong written and verbal communication</li><li>Possess ability to understand interrelationship between systems and component equipment</li><li>Demonstrate ability to work with others in supplying information and seeking assistance as necessary</li><li>Demonstrate willingness and capabilities to assume leadership roles</li></ul>Job Type &amp; LocationThis is a Permanent position based out of New Albany, OH.Pay and BenefitsThe pay range for this position is $35.00 - $45.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully remote position.Application DeadlineThis position is anticipated to close on Mar 3, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Protection And Control Engineer PE (Remote)

Position SummaryActalent Services, LLC connects passion with purpose. We are supporting critical engineering and sciences initiatives that advance how companies serve the world. With almost 40 years of experience, our scalable talent solutions and engineering and sciences services provide the expertise our customers need to achieve more.The position falls within the Protection and Controls Department of the organization. The engineer will complete protection and control projects that support our customer. They will work with in-house and client engineers and designers. They will provide, coordinate, and conduct training to lower level engineers.Primary Duties and Responsibilities<ul><li>Work on green-field and brown-field (retrofit) Protection and Control Projects in substations</li><li>Set relays and conduct relay setting calculations utilizing ASPEN, AcSELerator 5010 (SEL), and GE URPC Software</li><li>Design settings in appropriate format then issue to assigned Protection and Controls Supervisor using IPS</li><li>Mark-up and review protection schematics and elementaries</li><li>Utilize MOB Port to review equipment and materials established by substation engineers for Protection Designers</li><li>Work with the following equipment: transformers, circuit breakers, buses, reactors, line disconnects, protective relays systems (SEL, ABB, etc.), and SCADA systems</li><li>Function as a project lead for protection and control projects</li><li>Perform all engineering and design activities with minimum direction</li><li>Lead, facilitate, and coordinate work activities of others within the work group, team, department, or those external to complete substation projects</li><li>Provide training and guidance to lower level employees</li><li>Identify and initiate corrective action when substation project objectives are not being met</li><li>Interpret codes and regulations and develop standards for construction projects</li><li>Promote engineering professionalism and standards</li><li>Develop, recommend, and implement plans by establishing goals, objectives, and requirements that include all scheduling, resources, and cont information for complex engineering</li><li>Position requires 10-15% travel to field substations</li></ul>Education and Experience Requirements<ul><li>Five to eight years of experience in utilities working with protection and controls</li><li>Five to eight years of experience completing engineering projects from start to finish</li><li>Five to eight years of experience setting relays and designing one line diagrams</li><li>Bachelor’s Degree in Electrical Engineering (ABET)</li><li>Master’s Degree in Electrical Engineering (ABET) will count toward years’ experience</li><li>A PE License is required</li></ul>Requisite Abilities and Skills<ul><li>Intermediate ability to perform design calculations such as battery sizing, AC and DC loads, system component selection, power transformer and circuit breaker selection, circuit protection, control and power cable selection and rating, bus bars, fittings, insulators, ground grid design, and lightning protection</li><li>Intermediate understanding of standards and codes such as IEEE, ANSI, NERC-PRC, NEC, and NESC</li><li>Possess intermediate understanding of protection and control equipment, relays, and fault analysis</li><li>Strong written and verbal communication</li><li>Possess ability to understand interrelationship between systems and component equipment</li><li>Demonstrate ability to work with others in supplying information and seeking assistance as necessary</li><li>Demonstrate willingness and capabilities to assume leadership roles</li></ul>Job Type &amp; LocationThis is a Permanent position based out of Tulsa, OK.Pay and BenefitsThe pay range for this position is $35.00 - $45.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully remote position.Application DeadlineThis position is anticipated to close on Mar 3, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Job Title: Wire Harness TechnicianJob DescriptionThe Wire Harness Technician will play a pivotal role in launching the first in-house wire harness manufacturing initiative. This position is responsible for building wire harnesses for production and pilot programs, developing a quality control and testing process, and supporting Engineering, Quality, and Electrical teams during prototype and validation activities.Responsibilities<ul><li>Build wire harnesses for VOG/harness stock outs, market fills, and production needs.</li><li>Produce and modify prototype harnesses for pilot vehicles, validations, and engineering evaluations.</li><li>Interpret and work from wiring diagrams, schematics, and build instructions.</li><li>Crimp, strip, route, tape, terminate, and test 12V harnesses using industry-standard tools and techniques.</li><li>Validate fit, form, and function of harnesses in vehicle applications.</li><li>Work with Quality and Engineering teams to develop an end-to-end quality control process.</li><li>Establish testing methods such as continuity, load testing, and pin checks.</li><li>Document inspection standards for harness builds and implement test fixtures or jigs for repeatable quality.</li><li>Maintain accurate build records, test logs, and traceability documentation.</li><li>Assist in developing workflows for the new harness build cell.</li><li>Perform time studies, cost analyses, and process evaluations.</li><li>Compare cost of in-house production versus supplier outsourcing and provide recommendations.</li><li>Identify efficiency opportunities and implement continuous improvement changes.</li><li>Maintain 5S standards in the harness area, ensuring organization, cleanliness, and tool management.</li><li>Collaborate with the Electrical Team to balance administrative and technical workloads.</li><li>Support Engineering and Quality with component evaluations, root-cause investigations, or supplier discussions as needed.</li><li>Participate in pilot builds, engineering reviews, and production readiness activities.</li><li>Share build insights and improvements as harness production scales.</li></ul>Essential Skills<ul><li>Hands-on experience building wire harnesses (12V automotive, upfitting, or similar).</li><li>Ability to read wiring diagrams, schematics, and work instructions.</li><li>Experience with harness testing and quality control, including continuity checks and test fixtures.</li><li>Understanding of automotive electrical systems, 12V circuits, lighting, alarms, and related components.</li><li>Strong documentation skills for test procedures, build logs, and time/cost studies.</li><li>Ability to work independently in a pilot/learning environment and adapt as processes evolve.</li><li>Familiarity with basic manufacturing tools such as crimpers, cutters, and stripping tools.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience developing a new manufacturing process or launching a new product line.</li><li>Understanding of lean manufacturing &amp; continuous improvement methodologies.</li><li>Experience building prototype harnesses or pilot-phase components.</li><li>Exposure to supplier cost comparisons or make-versus-buy analysis.</li><li>Knowledge of upfitting or vehicle modification operations.</li><li>Experience collaborating cross-functionally with Quality, Engineering, and Production teams.</li></ul>Work EnvironmentThis role involves working in a newly established harness cell, helping set up workflow, quality checks, and layout. The environment is hands-on, including crimping, routing, assembly, testing, and documentation. There will be collaboration with Engineering, Quality, and Electrical teams in a startup-like setting within a manufacturing context, requiring flexibility, problem-solving, and experimentation. The technician will support both production needs and prototype/pilot builds for new vehicle programs while following and maintaining 5S and safe work practices.Job Type &amp; LocationThis is a Contract to Hire position based out of Adrian, MI.Pay and BenefitsThe pay range for this position is $25.00 - $35.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Adrian,MI.Application DeadlineThis position is anticipated to close on Feb 24, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Prototype Technician

Job Title: Psychometric RaterJob DescriptionThe primary goal of this role is to increase patient volume for psychometric assessments. The position currently has two part-time raters working from Tuesday to Thursday, and there is a need to expand coverage to five days a week to eliminate bottlenecks in patient screening. The facility is currently seeing approximately 10 patients per week, with variability depending on the lengths of the test batteries. Typical visits last around four hours, with longer durations for patients with more significant cognitive decline. The site is actively conducting seven Alzheimer's trials, with two more launching soon, and three studies are currently enrolling with potential for additional ones.Responsibilities<ul><li>Conduct psychometric assessments to increase patient volume.</li><li>Administer Alzheimer's-related scales and assessments.</li><li>Ensure coverage for patient screenings five days a week.</li><li>Prepare for patient visits by reviewing scales for approximately one hour beforehand.</li><li>Collaborate with clinical research coordinators and research assistants to manage scheduling and ensure rater availability.</li></ul>Essential Skills<ul><li>Experience administering Alzheimer's-related scales.</li><li>Completion of required scales at least 10 times within the last 12 months.</li><li>1–3 years of experience for sponsor approval.</li><li>Master's Degree in related field required.</li><li>Proficiency with Alzheimer’s-related scales including CDR, ADCS-ADL, ADAS-Cog, NPI, MMSE, MoCA, CGI-C/CGI-S, and CIBIS/CIBIC.</li></ul>Additional Skills &amp; Qualifications<ul><li>Clinical research experience is strongly preferred.</li><li>Experience in clinical rating is essential.</li></ul>Work EnvironmentThis is a fully onsite role with a duration of 6–12 months, offering the potential for permanent hire if the fit is strong and if business permits. Candidates can choose full-time or PRN status, with a minimum of two days per week required for PRN. The work schedule is Monday through Friday. The role involves collaboration with a team consisting of a project manager, principal investigator, sub-investigator, three clinical research coordinators, two research assistants, and two PRN raters. The position does not offer a remote work option.Job Type &amp; LocationThis is a Contract position based out of Dayton, OH.Pay and BenefitsThe pay range for this position is $25.00 - $35.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Dayton,OH.Application DeadlineThis position is anticipated to close on Feb 27, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Psychometric Rater

Job Title: Psychometric RaterJob DescriptionThe primary goal of this role is to increase patient volume for psychometric assessments. The position currently has two part-time raters working from Tuesday to Thursday, and there is a need to expand coverage to five days a week to eliminate bottlenecks in patient screening. The facility is currently seeing approximately 10 patients per week, with variability depending on the lengths of the tests. Typical visits last around four hours, with longer durations for patients with more significant cognitive decline. The site is actively conducting seven Alzheimer's trials, with two more launching soon, and three studies are currently enrolling with potential for additional ones.Responsibilities<ul><li>Conduct psychometric assessments to increase patient volume.</li><li>Administer Alzheimer's-related scales and assessments.</li><li>Ensure coverage for patient screenings five days a week.</li><li>Prepare for patient visits by reviewing scales for approximately one hour beforehand.</li><li>Collaborate with clinical research coordinators and research assistants to manage scheduling and ensure rater availability.</li></ul>Require Skills &amp; Experience<ul><li>Experience administering Alzheimer's-related scales.</li><li>Completion of required scales at least 10 times within the last 12 months.</li><li>1–3 years of experience for sponsor approval.</li><li>Master's Degree in related field required.</li><li>Proficiency with Alzheimer’s-related scales including CDR, ADCS-ADL, ADAS-Cog, NPI, MMSE, MoCA, CGI-C/CGI-S, and CIBIS/CIBIC.</li></ul>Additional Skills &amp; Qualifications<ul><li>Clinical research experience is strongly preferred.</li><li>Experience in clinical rating is essential.</li></ul>Work EnvironmentThis is a fully onsite role with a duration of 6–12 months, offering the potential for permanent hire if the fit is strong and if business permits. Candidates can choose full-time or PRN status, with a minimum of two days per week required for PRN. The work schedule is Monday through Friday. The role involves collaboration with a team consisting of a project manager, principal investigator, sub-investigator, three clinical research coordinators, two research assistants, and two PRN raters. The position does not offer a remote work option.Job Type &amp; LocationThis is a Contract position based out of Dayton, OH.Pay and BenefitsThe pay range for this position is $25.00 - $35.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Dayton,OH.Application DeadlineThis position is anticipated to close on Feb 27, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Job Title: Pump TechnicianJob DescriptionWe are seeking a pump technician who possesses 1+ years of experience in a mechanical or environmental setting. This technician will support this landfill site with routine and non-routine maintenance. The role involves tuning wellfields, pump maintenance (including pulling, cleaning/service, and replacement), and extensive work with SEMs and probes, which requires substantial walking across landfills.Responsibilities<ul><li>Perform routine and non-routine maintenance on wellfields.</li><li>Conduct pump maintenance, including pulling, cleaning, servicing, and replacement.</li><li>Work extensively with SEMs and probes, requiring substantial walking on foot.</li></ul>Essential Skills<ul><li>Proficiency with computer software is a plus.</li><li>Mechanical aptitude for field sampling and troubleshooting.</li><li>Familiarity with environmental testing and data collection.</li></ul>Additional Skills &amp; Qualifications<ul><li>ISCO pipe fusion certification is a plus.</li><li>40 HR HAZWOPER or 8 HR Refresher is a plus. Otherwise we will get you this training prior to being onsite.</li></ul>Work EnvironmentThe work environment includes landfills with a GCCS methane system leading to a gas-to-energy plant. The role involves extensive walking and working outdoors, supporting a culture of professionalism and security within one of the largest and most respected environmental engineering firms in the US. working with landfill gas. We have a very low turnover/attrition rate and provide reliable weekly pay!Job Type &amp; LocationThis is a Contract to Hire position based out of Bishopville, SC.Pay and BenefitsThe pay range for this position is $23.00 - $23.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Bishopville,SC.Application DeadlineThis position is anticipated to close on Feb 25, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Pump Technician

Job Title: QA AssociateJob DescriptionThe QA Associate is responsible for the rigorous review, verification, and archival of batch records and associated documentation to ensure compliance with internal SOPs, cGMP, and FDA regulations. This role involves close collaboration with production, warehouse, and quality teams to resolve discrepancies and maintain data integrity.Responsibilities<ul><li>Perform comprehensive batch record reviews for completeness, accuracy, and compliance with GDP and SOPs.</li><li>Review supporting documentation including logbooks, protocols, packaging records, and inventory records.</li><li>Collaborate with production and management to resolve discrepancies or missing information in batch records.</li><li>Scan and archive completed records into the electronic database and physical storage system.</li><li>Input data into warehouse management systems (e.g., Dynamics 365) and quality systems (e.g., Reliance).</li><li>Ensure inventory values and documentation are accurately recorded.</li><li>Participate in continuous improvement efforts and assist in training production staff on documentation best practices.</li><li>Cross-train in other QA Associate functions such as Document Control and Inventory Control.</li><li>Issue and control batch records, cleaning records, test sheets, and logbooks.</li><li>Maintain and control the company lot number system and ensure proper documentation flow.</li></ul>Essential Skills<ul><li>High School Diploma or GED required; Associate’s or Bachelor’s degree in a scientific or technical field preferred.</li><li>1+ year of experience in pharmaceutical QA or FDA-regulated environment preferred.</li><li>Strong attention to detail and ability to work in a fast-paced, documentation-heavy environment.</li><li>Proficient in Microsoft Office and comfortable using ERP and quality systems (e.g., Dynamics 365, Reliance).</li><li>Excellent written and verbal communication skills.</li><li>Ability to work independently and collaboratively with minimal supervision.</li></ul>Additional Skills &amp; Qualifications<ul><li>Strong interpersonal skills; able to work respectfully with cross-functional teams.</li><li>Self-motivated and organized with a high level of accountability.</li><li>Willingness to learn and adapt to evolving processes and systems.</li></ul>Work EnvironmentThe position operates Monday through Friday with a flexible start time between 7:00 - 8:30 AM, with shifts lasting 8-9 hours. The work is primarily desk-based in a shared office setting, with 90% of tasks performed at a desk. Occasionally, lifting up to 50 lbs may be required. The manufacturing building is dusty due to the powdered products they produce and is not a sterile environment. The team comprises 3 Inspectors, 1 Supervisor, 3 Batch Record Reviewers, 1 Doc Control, and 1 Inventory Control member.#STLSCIJob Type &amp; LocationThis is a Contract to Hire position based out of Saint Louis, MO.Pay and BenefitsThe pay range for this position is $22.00 - $26.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Saint Louis,MO.Application DeadlineThis position is anticipated to close on Mar 4, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

QA Associate

Job Title: QA AssociateJob DescriptionThe QA Associate is responsible for the rigorous review, verification, and archival of batch records and associated documentation to ensure compliance with internal SOPs, cGMP, and FDA regulations. This role involves close collaboration with production, warehouse, and quality teams to resolve discrepancies and maintain data integrity.Responsibilities<ul><li>Perform comprehensive batch record reviews for completeness, accuracy, and compliance with GDP and SOPs.</li><li>Review supporting documentation including logbooks, protocols, packaging records, and inventory records.</li><li>Collaborate with production and management to resolve discrepancies or missing information in batch records.</li><li>Scan and archive completed records into the electronic database and physical storage system.</li><li>Input data into warehouse management systems (e.g., Dynamics 365) and quality systems (e.g., Reliance).</li><li>Ensure inventory values and documentation are accurately recorded.</li><li>Participate in continuous improvement efforts and assist in training production staff on documentation best practices.</li><li>Cross-train in other QA Associate functions such as Document Control and Inventory Control.</li><li>Issue and control batch records, cleaning records, test sheets, and logbooks.</li><li>Maintain and control the company lot number system and ensure proper documentation flow.</li></ul>Essential Skills<ul><li>High School Diploma or GED required; Associate’s or Bachelor’s degree in a scientific or technical field preferred.</li><li>1+ year of experience in pharmaceutical QA or FDA-regulated environment preferred.</li><li>Strong attention to detail and ability to work in a fast-paced, documentation-heavy environment.</li><li>Proficient in Microsoft Office and comfortable using ERP and quality systems (e.g., Dynamics 365, Reliance).</li><li>Excellent written and verbal communication skills.</li><li>Ability to work independently and collaboratively with minimal supervision.</li></ul>Additional Skills &amp; Qualifications<ul><li>Strong interpersonal skills; able to work respectfully with cross-functional teams.</li><li>Self-motivated and organized with a high level of accountability.</li><li>Willingness to learn and adapt to evolving processes and systems.</li></ul>Work EnvironmentThe position operates Monday through Friday with a flexible start time between 7:00 - 8:30 AM, with shifts lasting 8-9 hours. The work is primarily desk-based in a shared office setting, with 90% of tasks performed at a desk. Occasionally, lifting up to 50 lbs may be required. The manufacturing building is dusty due to the powdered products they produce and is not a sterile environment. The team comprises 3 Inspectors, 1 Supervisor, 3 Batch Record Reviewers, 1 Doc Control, and 1 Inventory Control member.#STLSCIJob Type &amp; LocationThis is a Contract to Hire position based out of Saint Louis, MO.Pay and BenefitsThe pay range for this position is $22.00 - $26.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Saint Louis,MO.Application DeadlineThis position is anticipated to close on Mar 5, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Job Title: QA Associate - Batch Record ReviewJob DescriptionPerform detailed batch record review for manufacturing, packaging, and labeling operations to ensure accuracy, completeness, and compliance with cGMP requirements, including in a sterile manufacturing facility. Verify that all critical process steps, test results, deviations, and yields are properly documented. Identify documentation errors, inconsistencies, or missing information and coordinate corrections with Manufacturing, Quality Control, and other departments.Responsibilities<ul><li>Review equipment cleaning logs, line clearance forms, and related production documents.</li><li>Support lot disposition activities by preparing QA documentation packets for final review.</li><li>Assist in investigating deviations, nonconformances, and CAPAs as needed.</li><li>Participate in internal audits and support external regulatory inspections.</li><li>Maintain QA documentation according to standard operating procedures.</li><li>Recommend process and documentation improvements to increase compliance and efficiency.</li></ul>Essential Skills<ul><li>Bachelor’s degree in Life Sciences, Chemistry, Biology, Engineering, or related discipline.</li><li>1–3+ years of experience in pharmaceutical, biotech, or regulated manufacturing environments.</li><li>Strong understanding of cGMP, FDA regulations, and batch documentation requirements.</li><li>Excellent attention to detail and strong organizational skills.</li><li>Ability to communicate effectively across multiple departments.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience with SAP is a plus.</li><li>Experience with some form of EMR is required.</li></ul>Work EnvironmentThe QA department is divided into two teams: QA Operations and QA Systems, with approximately 8 people across both teams. The QA Operations team handles batch record review, AQL, inspections, temperature checks, and label and vial review, while the QA Systems team manages document control, QMCS, calibration, change controls, deviations, investigations, and CAPAs. Employees may have responsibilities in both departments. The work schedule is Monday through Friday, from 8 am to 4:30 pm.Job Type &amp; LocationThis is a Contract to Hire position based out of Port Washington, NY.Pay and BenefitsThe pay range for this position is $28.85 - $31.25/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Port Washington,NY.Application DeadlineThis position is anticipated to close on Feb 27, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

QA Associate - Batch Record Review

<h2 style="text-align:center;">Job Title: QA Associate - Batch Record Review</h2>Job DescriptionPerform detailed batch record review for manufacturing, packaging, and labeling operations to ensure accuracy, completeness, and compliance with cGMP requirements, including in a sterile manufacturing facility. Verify that all critical process steps, test results, deviations, and yields are properly documented. Identify documentation errors, inconsistencies, or missing information and coordinate corrections with Manufacturing, Quality Control, and other departments.Responsibilities<ul><li>Review equipment cleaning logs, line clearance forms, and related production documents.</li><li>Support lot disposition activities by preparing QA documentation packets for final review.</li><li>Assist in investigating deviations, nonconformances, and CAPAs as needed.</li><li>Participate in internal audits and support external regulatory inspections.</li><li>Maintain QA documentation according to standard operating procedures.</li><li>Recommend process and documentation improvements to increase compliance and efficiency.</li></ul>Essential Skills<ul><li>Bachelor’s degree in Life Sciences, Chemistry, Biology, Engineering, or related discipline.</li><li>1–3+ years of experience in pharmaceutical, biotech, or regulated manufacturing environments.</li><li>Strong understanding of cGMP, FDA regulations, and batch documentation requirements.</li><li>Excellent attention to detail and strong organizational skills.</li><li>Ability to communicate effectively across multiple departments.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience with SAP is a plus.</li><li>Experience with some form of EMR is required.</li></ul>Work EnvironmentThe QA department is divided into two teams: QA Operations and QA Systems, with approximately 8 people across both teams. The QA Operations team handles batch record review, AQL, inspections, temperature checks, and label and vial review, while the QA Systems team manages document control, QMCS, calibration, change controls, deviations, investigations, and CAPAs. Employees may have responsibilities in both departments. The work schedule is Monday through Friday, from 8 am to 4:30 pm.Job Type &amp; LocationThis is a Contract to Hire position based out of Port Washington, NY.Pay and BenefitsThe pay range for this position is $28.85 - $31.25/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Port Washington,NY.Application DeadlineThis position is anticipated to close on Feb 28, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

<h2>**HIRING NOW: Quality Assurance Documentation Associate**</h2>Interested in this role? Reach out directly to apply TODAY to Grace Williams at grawilliams@actalentservices .com | Call/Text 317-567 6610SummaryAs a QA Associate, you will play a crucial role in ensuring the quality and compliance of our products and packaging. You will be responsible for reviewing and analyzing data, supporting quality systems, and ensuring adherence to applicable procedures and standards.Responsibilities<ul><li>Provide support to Quality systems.</li><li>Organize, critically review, and present information in accordance with written procedures.</li><li>Provide support for the production area.</li><li>Apply and obtain statistical analysis.</li><li>Write, review, and revise GMP standard operating procedures.</li><li>Track, maintain, and critically review manufacturing records.</li><li>Maintain communication with QC lab regarding test results pertinent to batch release.</li><li>Maintain communication with Supply Chain Representatives to ensure timely release of batch manufacturing records.</li><li>Approve raw materials for use in production areas and evaluate vendor COA’s.</li><li>Print and prepare batch manufacturing records as requested by Supply Chain.</li><li>Create or prepare Certificates of Analysis as requested by Customer Service Representatives.</li><li>Perform inbound Quality Analysis and receipt for printed packaging materials.</li><li>Monitor temperature records of bulk material received for Companion Animal Products.</li><li>Own, track, and route documents in Veeva Vault for editing, review, and approval.</li></ul>Essential Skills<ul><li>Quality Assurance experience</li><li>Batch Record knowledge</li><li>GMP knowledge</li><li>Batch Record Review skills</li><li>Pharmaceutical and Life Science experience</li><li>Quality Inspection</li><li>Titration</li><li>Quality Documentation</li><li>pH Testing</li><li>Analytical skills</li><li>Biology and Chemistry knowledge</li><li>QA Testing, Checking, and Documentation</li><li>SOP Review</li></ul>Additional Skills &amp; Qualifications<ul><li>B.S./A.S. Degree in a related field OR 12+ months of QA/GMP experience without a degree</li><li>Strong communication, documentation, and math skills</li><li>Proficiency with computers</li><li>Attention to detail</li><li>Batch Record Review experience (nice to have)</li></ul><h2>INTERESTED IN THIS ROLE? SEE BELOW TO APPLY NOW FOR IMMEDIATE CONSIDERTATION:</h2>*Interview availability this week*<ul><li>I am scheduling interviews for this position and conducting phone interviews as early as TODAY. All candidates will be considered immediately within 24 hours of applying directly to Grace Williams.</li><li>HOW TO APPLY DIRECTLY: Email your updated resume, brief intro about your interest, preferred method of communication for you (i.e., call, email, text) to grawilliams@actalentservices. com or call/text me directly at (317-567 -6610)</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Clinton, IN.Pay and BenefitsThe pay range for this position is $20.00 - $25.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Clinton,IN.Application DeadlineThis position is anticipated to close on Mar 2, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

QA Associate - HIRING NOW

<h2>**HIRING NOW: Quality Assurance Documentation Associate**</h2>Interested in this role? Reach out directly to apply TODAY to Sneha Prakash snprakash@actalentservices. com or call 317 548 1234 at the earliestSummaryAs a QA Associate, you will play a crucial role in ensuring the quality and compliance of our products and packaging. You will be responsible for reviewing and analyzing data, supporting quality systems, and ensuring adherence to applicable procedures and standards.Responsibilities<ul><li>Provide support to Quality systems.</li><li>Organize, critically review, and present information in accordance with written procedures.</li><li>Provide support for the production area.</li><li>Apply and obtain statistical analysis.</li><li>Write, review, and revise GMP standard operating procedures.</li><li>Track, maintain, and critically review manufacturing records.</li><li>Maintain communication with QC lab regarding test results pertinent to batch release.</li><li>Maintain communication with Supply Chain Representatives to ensure timely release of batch manufacturing records.</li><li>Approve raw materials for use in production areas and evaluate vendor COA’s.</li><li>Print and prepare batch manufacturing records as requested by Supply Chain.</li><li>Create or prepare Certificates of Analysis as requested by Customer Service Representatives.</li><li>Perform inbound Quality Analysis and receipt for printed packaging materials.</li><li>Monitor temperature records of bulk material received for Companion Animal Products.</li><li>Own, track, and route documents in Veeva Vault for editing, review, and approval.</li></ul>Essential Skills<ul><li>Quality Assurance experience</li><li>Batch Record knowledge</li><li>GMP knowledge</li><li>Batch Record Review skills</li><li>Pharmaceutical and Life Science experience</li><li>Quality Inspection</li><li>Titration</li><li>Quality Documentation</li><li>pH Testing</li><li>Analytical skills</li><li>Biology and Chemistry knowledge</li><li>QA Testing, Checking, and Documentation</li><li>SOP Review</li></ul>Additional Skills &amp; Qualifications<ul><li>B.S./A.S. Degree in a related field OR 12+ months of QA/GMP experience without a degree</li><li>Strong communication, documentation, and math skills</li><li>Proficiency with computers</li><li>Attention to detail</li><li>Batch Record Review experience (nice to have)</li></ul><h2>INTERESTED IN THIS ROLE? SEE BELOW TO APPLY NOW FOR IMMEDIATE CONSIDERTATION:</h2>*Interview availability this week*<ul><li>I am scheduling interviews for this position and conducting phone interviews as early as TODAY. All candidates will be considered immediately within 24 hours of applying directly to Sneha Prakash </li><li>HOW TO APPLY DIRECTLY: Email your updated resume, brief intro about your interest, preferred method of communication for you (i.e., call, email, text) to Sneha Prakash snprakash@actalentservices. com or call 317 548 1234 at the earliest</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Clinton, IN.Pay and BenefitsThe pay range for this position is $20.00 - $25.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Clinton,IN.Application DeadlineThis position is anticipated to close on Feb 26, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Job Title: QA AuditorJob DescriptionWe are seeking a dedicated Quality Assurance Auditor to join our team, offering opportunities on the 1st, 2nd, and 3rd shifts. A differential will be applied to 2nd and 3rd shifts. This role is crucial for performing inspection duties such as line coverage, audit reviews, and monitoring charts. The position requires the completion of all necessary paperwork and data entry specific to quality assurance monitoring.Responsibilities<ul><li>Perform line checks, including in-process testing, component verification, barcode operation, sample review, aseptic monitoring, and end-item inspection.</li><li>Complete line clearance inspections and review area logs for proper documentation before lot processing.</li><li>Check in all components before production use.</li><li>Review and approve production records and associated paperwork, ensuring all calculations are correct.</li><li>Conduct chart, log, product, and document reviews.</li><li>Perform batch record reviews for accuracy and compliance with company procedures.</li><li>Oversee documentation of production interventions as needed.</li><li>Conduct area purges, including packaging and vial wash.</li><li>Perform shelf reserve sampling, reviews, TRRs, and documentation.</li><li>Successfully complete Manual Inspection Qualification for vial inspections.</li><li>Attend meetings as required or requested.</li><li>Promote a safe and harmonious work environment.</li><li>Maintain compliance with SOPs, GMPs, and all company policies.</li><li>Perform other duties as assigned or required.</li></ul>Essential Skills<ul><li>Audit and quality assurance experience.</li><li>Knowledge of compliance, internal auditing, and FDA regulations.</li><li>Associates degree in science or a related field from a regionally accredited institution.</li><li>At least 1 year of quality assurance experience in a pharmaceutical or highly regulated industry.</li><li>Proficiency in Microsoft Office programs and general computer functions.</li><li>Experience in quality auditing practices.</li><li>Understanding of processes relevant to quality compliance, regulatory and development processes, and cGMP requirements for pharmaceuticals.</li><li>Knowledge of HACCP and other audit schemes.</li><li>Ability to manage multiple projects or tasks simultaneously.</li></ul>Additional Skills &amp; Qualifications<ul><li>Advanced problem safety sensitivity and the ability to recognize safety issues.</li><li>Time management skills for personal and team tasks.</li><li>Vigilance in quality and compliance.</li><li>Ability to inspect and coach others in line with company SOPs.</li><li>Critical thinking and advanced interpersonal and communication skills.</li><li>Capability to effectively present the company's quality strategy to various stakeholders.</li><li>Flexibility in work hours and ability to provide motivational support.</li><li>Maintain a professional, positive attitude.</li><li>Advanced project management and documentation skills.</li><li>Effective training and instructional skills.</li></ul>Work EnvironmentThe work environment includes clean rooms, labs, and production areas.Job Type &amp; LocationThis is a Contract to Hire position based out of Syracuse, NY.Pay and BenefitsThe pay range for this position is $24.00 - $30.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Syracuse,NY.Application DeadlineThis position is anticipated to close on Feb 28, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

QA Auditor

Job Title: QA Deviation InvestigatorJob DescriptionThe QA Deviation Investigator is responsible for analyzing and investigating deviations or non-conformances within the organization. The role involves using problem-solving tools like root cause analysis, collecting and analyzing data to identify patterns, trends, or potential causes, and documenting findings comprehensively. This position requires collaboration with various departments to gather information, evaluate causal factors, and implement corrective and preventive actions (CAPAs). Additionally, the investigator will provide timely written documentation of investigations and communicate recommendations based on investigation outcomes. Participation in client communications and responses, working closely with program team leads, quality, and management is also expected.Responsibilities<ul><li>Analyze and investigate deviations or non-conformances using problem-solving tools like root cause analysis.</li><li>Collect relevant data and information related to deviations, and analyze it to identify patterns, trends, or potential causes.</li><li>Document findings in a comprehensive and objective manner, ensuring accurate recording of all relevant information.</li><li>Collaborate with various departments to gather information, evaluate causal factors, and implement corrective and preventive actions (CAPAs).</li><li>Provide timely written documentation of investigations and communicate recommendations based on investigation outcomes.</li><li>Participate in client communications and responses, working closely with program team leads, quality, and management.</li></ul>Essential Skills<ul><li>Experience in CAPA, quality assurance, root cause analysis, deviations, pharmaceutical, GMP, FDA, deviations and root cause analysis.</li><li>Technical writing proficiency.</li><li>Knowledge of quality processes and six sigma methodologies.</li></ul>Additional Skills &amp; Qualifications<ul><li>BS/BA in biology, biochemistry, chemistry, or other science-related field.</li><li>1+ years of experience in direct utilization of problem-solving tools (Root Cause Analysis and/or LEAN/six sigma experience) with demonstrated success.</li><li>1+ years of experience in technical writing and/or deviation writing.</li><li>3+ years of experience working in a regulated environment, preferably in biologics/pharmaceuticals.</li><li>Solid technical writing and communication skills.</li><li>Ability to evaluate data and make recommendations based on trends and trend analysis.</li><li>Ability to work effectively in a fast-paced environment and prioritize tasks.</li><li>Ability to facilitate meetings for desired outcomes.</li></ul>Work EnvironmentThis position requires working Monday-Friday from 8am-5pm with flexibility in start and end times, but core hours of 9am-3pm must be adhered to. The role involves collaboration with any department necessary for addressing deviations, not limited to upstream or downstream processes.Job Type &amp; LocationThis is a Contract position based out of Berkeley, MO.Pay and BenefitsThe pay range for this position is $36.00 - $40.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Berkeley,MO.Application DeadlineThis position is anticipated to close on Feb 27, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

QA Deviation Investigator

<h2 style="text-align:center;">QA Deviation Investigator</h2>Job DescriptionThe QA Deviation Investigator is responsible for analyzing and investigating deviations or non-conformances within the organization. The role involves using problem-solving tools like root cause analysis, collecting and analyzing data to identify patterns, trends, or potential causes, and documenting findings comprehensively. This position requires collaboration with various departments to gather information, evaluate causal factors, and implement corrective and preventive actions (CAPAs). Additionally, the investigator will provide timely written documentation of investigations and communicate recommendations based on investigation outcomes. Participation in client communications and responses, working closely with program team leads, quality, and management is also expected.PAY - $36-$40/hourResponsibilities<ul><li>Analyze and investigate deviations or non-conformances using problem-solving tools like root cause analysis.</li><li>Collect relevant data and information related to deviations, and analyze it to identify patterns, trends, or potential causes.</li><li>Document findings in a comprehensive and objective manner, ensuring accurate recording of all relevant information.</li><li>Collaborate with various departments to gather information, evaluate causal factors, and implement corrective and preventive actions (CAPAs).</li><li>Provide timely written documentation of investigations and communicate recommendations based on investigation outcomes.</li><li>Participate in client communications and responses, working closely with program team leads, quality, and management.</li></ul>Essential Skills<ul><li>Experience in CAPA, quality assurance, root cause analysis, deviations, pharmaceutical, GMP, FDA, deviations and root cause analysis.</li><li>Technical writing proficiency.</li><li>Knowledge of quality processes and six sigma methodologies.</li></ul>Additional Skills &amp; Qualifications<ul><li>BS/BA in biology, biochemistry, chemistry, or other science-related field.</li><li>1+ years of experience in direct utilization of problem-solving tools (Root Cause Analysis and/or LEAN/six sigma experience) with demonstrated success.</li><li>1+ years of experience in technical writing and/or deviation writing.</li><li>3+ years of experience working in a regulated environment, preferably in biologics/pharmaceuticals.</li><li>Solid technical writing and communication skills.</li><li>Ability to evaluate data and make recommendations based on trends and trend analysis.</li><li>Ability to work effectively in a fast-paced environment and prioritize tasks.</li><li>Ability to facilitate meetings for desired outcomes.</li></ul>Work EnvironmentThis position requires working Monday-Friday from 8am-5pm with flexibility in start and end times, but core hours of 9am-3pm must be adhered to. The role involves collaboration with any department necessary for addressing deviations, not limited to upstream or downstream processes.Job Type &amp; LocationThis is a Contract position based out of Berkeley, MO.Pay and BenefitsThe pay range for this position is $36.00 - $40.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Berkeley,MO.Application DeadlineThis position is anticipated to close on Feb 24, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

QA Deviation InvestigatorDescription• Analyze and investigate deviations or non-conformances, using problem-solving tools like root cause analysis.• Collect relevant data and information related to the deviation, and analyze it to identify patterns, trends, or potential causes.• Document findings in a comprehensive and objective manner, ensuring accurate recording of all relevant information.• Collaborate with various departments to gather information, evaluate causal factors, and implement corrective and preventive actions (CAPAs).• Provide timely written documentation of investigations and communicate recommendations based on investigation outcomes.• Participate in client communications and responses, working closely with program team leads, quality, and management.PAY - $38-$43/hourSkillscapa, quality assurance, root cause analysis, deviations, pharmaceutical, gmp, fda, technical writing, quality processes, six sigmaTop Skills Detailscapa,quality assurance,root cause analysis,deviations,pharmaceutical,gmp,fdaAdditional Skills &amp; QualificationsEducation:• BS/BA in biology, biochemistry, chemistry, or another science-related field.Experience:• 1+ years of experience in direct utilization of problem-solving tools (Root Cause Analysis and/or LEAN/six sigma experience) with demonstrated success.• 1+ years of experience in technical writing and/or deviation writing.• 3+ years of experience working in a regulated environment, preferably in biologics/pharmaceuticals.Knowledge, Skills, and Abilities:• Solid technical writing and communication skills.• Ability to evaluate data and make recommendations based on trends and trend analysis.• Ability to work effectively in a fast-paced environment and prioritize tasks.• Ability to facilitate meetings for desired outcomes.Experience LevelExpert LevelJob Type &amp; LocationThis is a Contract position based out of Berkeley, MO.Pay and BenefitsThe pay range for this position is $38.00 - $43.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Berkeley,MO.Application DeadlineThis position is anticipated to close on Feb 25, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Job Title: QA Deviation InvestigatorJob DescriptionThe QA Deviation Investigator is responsible for analyzing and investigating deviations or non-conformances within the organization. The role involves using problem-solving tools like root cause analysis, collecting and analyzing data to identify patterns, trends, or potential causes, and documenting findings comprehensively. This position requires collaboration with various departments to gather information, evaluate causal factors, and implement corrective and preventive actions (CAPAs). Additionally, the investigator will provide timely written documentation of investigations and communicate recommendations based on investigation outcomes. Participation in client communications and responses, working closely with program team leads, quality, and management is also expected.Responsibilities<ul><li>Analyze and investigate deviations or non-conformances using problem-solving tools like root cause analysis.</li><li>Collect relevant data and information related to deviations, and analyze it to identify patterns, trends, or potential causes.</li><li>Document findings in a comprehensive and objective manner, ensuring accurate recording of all relevant information.</li><li>Collaborate with various departments to gather information, evaluate causal factors, and implement corrective and preventive actions (CAPAs).</li><li>Provide timely written documentation of investigations and communicate recommendations based on investigation outcomes.</li><li>Participate in client communications and responses, working closely with program team leads, quality, and management.</li></ul>Essential Skills<ul><li>Experience in CAPA, quality assurance, root cause analysis, deviations, pharmaceutical, GMP, FDA, deviations and root cause analysis.</li><li>Technical writing proficiency.</li><li>Knowledge of quality processes and six sigma methodologies.</li></ul>Additional Skills &amp; Qualifications<ul><li>BS/BA in biology, biochemistry, chemistry, or other science-related field.</li><li>1+ years of experience in direct utilization of problem-solving tools (Root Cause Analysis and/or LEAN/six sigma experience) with demonstrated success.</li><li>1+ years of experience in technical writing and/or deviation writing.</li><li>3+ years of experience working in a regulated environment, preferably in biologics/pharmaceuticals.</li><li>Solid technical writing and communication skills.</li><li>Ability to evaluate data and make recommendations based on trends and trend analysis.</li><li>Ability to work effectively in a fast-paced environment and prioritize tasks.</li><li>Ability to facilitate meetings for desired outcomes.</li></ul>Work EnvironmentThis position requires working Monday-Friday from 8am-5pm with flexibility in start and end times, but core hours of 9am-3pm must be adhered to. The role involves collaboration with any department necessary for addressing deviations, not limited to upstream or downstream processes.Job Type &amp; LocationThis is a Contract position based out of St. Louis, MO.Pay and BenefitsThe pay range for this position is $36.00 - $40.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in St. Louis,MO.Application DeadlineThis position is anticipated to close on Feb 24, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

QA Deviation Investigator (Pharma Manufacturing)

Job Title: QA Engineer - Kubernetes/Container DeploymentJob DescriptionWe are seeking an experienced engineer with a strong background in Kubernetes, containerized application deployment, and testing environments. This role is ideal for someone who is transitioning from a traditional engineering role into quality assurance and testing. The position focuses on white box testing, with an emphasis on inspecting the deployment of pods and containers, and assessing their health and performance.Responsibilities<ul><li>Perform white box testing by inspecting pods, containers, and smaller components.</li><li>Conduct functional testing, including UI inspections and resource utilization analysis.</li><li>Develop and execute test plans and automation scripts using Selenium, Cucumber, and WebDriverIO.</li><li>Assess and inspect deployments, ensuring they are up and healthy, and identify any bottlenecks or resource stress points.</li><li>Leverage AI technologies to enhance the testing environment.</li><li>Work with CI/CD pipelines and DevOps tools such as Terraform, Docker, and Kubernetes.</li></ul>Essential Skills<ul><li>Minimum of 1 year in a pure testing role and at least 3 years in a containerized environment.</li><li>Proficiency in Kubernetes and Docker, with AWS experience preferred.</li><li>Strong experience in Python, with knowledge of object-oriented programming.</li><li>Familiarity with automation tools such as Selenium, Cucumber, and WebDriverIO.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience with AI technologies is a significant advantage.</li><li>Understanding of DevOps tools like Terraform and containerized applications.</li><li>Ability to perform performance assessments, identifying bottlenecks and resource stress points.</li></ul>Work EnvironmentThis position offers a hybrid work environment located in Morrisville, NC, with in-office work required on Tuesdays and Thursdays.Job Type &amp; LocationThis is a Contract position based out of Morrisville, NC.Pay and BenefitsThe pay range for this position is $55.00 - $65.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a hybrid position in Morrisville,NC.Application DeadlineThis position is anticipated to close on Feb 21, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

QA Engineer

Job Title: QA Inspector IIIJob DescriptionAs a QA Inspector I, you will play a vital role in ensuring the quality and compliance of our manufacturing processes. You will be responsible for conducting room and equipment cleaning checks, documenting cleaning activities, and verifying materials. You will also monitor and maintain the reject cage, perform daily balance verifications, and ensure temperature and humidity levels are within specified standards. This position requires strict adherence to company policies, safety requirements, cGMP, and SOPs.Responsibilities<ul><li>Perform room and equipment cleaning checks prior to any activities.</li><li>Conduct daily rounds of the warehouse to ensure compliance.</li><li>Document cleaning activities in logbooks and checklists.</li><li>Physically release materials after receiving and reviewing release reports from QA.</li><li>Verify materials against incoming and release documents and material labels.</li><li>Monitor and maintain the reject cage.</li><li>Perform daily verification of balances.</li><li>Monitor temperature and humidity as per SOP.</li><li>Maintain and file documents.</li><li>Adhere to company policies, safety requirements, cGMP, and SOPs.</li><li>Perform other duties as assigned by the supervisor.</li></ul>Essential Skills<ul><li>Quality assurance</li><li>Line inspection</li><li>Pharmaceutical knowledge</li><li>Document review</li><li>Line clearance</li><li>Quality inspection</li><li>Batch record management</li><li>GMP knowledge</li><li>Document control</li></ul>Additional Skills &amp; Qualifications<ul><li>3 - 10 years of experience in QA line inspecting for pharmaceuticals.</li><li>Familiarity with GMP standards and regulations.</li><li>High School diploma.</li><li>Proficiency in reading and writing English.</li></ul>Work EnvironmentThis role is set within a manufacturing environment for a pharmaceutical company. The inspector will oversee 1-3 production lines at a time. The position offers holiday pay and one week of vacation. Overtime is available based on manufacturing needs. Salary is determined by experience and interview performance.Job Type &amp; LocationThis is a Permanent position based out of Hauppauge, NY.Pay and BenefitsThe pay range for this position is $56160.00 - $62400.00/yr.Comprehensive health coverage – Medical, dental, and vision insurance options are offered, with coverage for employees and eligible dependents
Retirement savings – 401(k) plan with employer matching contributions to support long‑term financial planning 
Paid time off – Includes paid holidays, vacation time, and sick leave, supporting work‑life balance 
Insurance protection – Life insurance and disability coverage are available as part of the benefits packageWorkplace TypeThis is a fully onsite position in Hauppauge,NY.Application DeadlineThis position is anticipated to close on Mar 5, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

QA Inspector III

Job Title: QA SupervisorJob DescriptionThe QA Supervisor will report to the Food Safety and Quality Manager and will directly oversee employees in the QA Lab. This role is essential in supervising and implementing quality programs while ensuring compliance with organizational policies and applicable laws.<h2>PAY - $70k - $90k</h2>Responsibilities<ul><li>Interview, hire, and train employees, while planning, assigning, and directing work.</li><li>Appraise performance, reward, and discipline employees as necessary.</li><li>Provide coverage and support in the absence of the Food Safety and Quality Manager.</li><li>Implement and continuously improve quality programs at the Elk Grove Village facility.</li><li>Identify and resolve problems, reporting food safety and quality issues to management.</li><li>Implement components of the quality assurance program, including data analysis, systems evaluation, and product assessment.</li><li>Direct hardware inspections and systems audits to ensure adherence to management system procedures.</li><li>Conduct raw material, in-process, and finished goods quality inspections.</li><li>Communicate effectively in Spanish, both written and orally.</li><li>Guide personnel in special test procedures to analyze product materials.</li><li>Compile and analyze test information to assess process or equipment efficiency and diagnose malfunctions.</li><li>Investigate product complaints and respond to vendors or customers as needed.</li><li>Establish or adjust work procedures to meet testing schedules.</li><li>Train lab staff on safety topics, quality procedures, and business updates.</li><li>Participate in and support corporate and plant initiatives, including GMP, HACCP, SQF, and other quality systems.</li><li>Engage in customer, regulatory, and third-party audits as required.</li></ul>Essential Skills<ul><li>Experience in food science, chemistry, biology, microbiology, sensory, food packaging systems, and/or food engineering.</li><li>3-7 years of practical experience in Food Safety, Quality Management, Production, or Project Management in the food industry.</li><li>Strong critical thinking, analytical, and problem-solving skills.</li><li>Excellent written and verbal communication skills.</li><li>Proficiency in Microsoft Word, Excel, and PowerPoint.</li><li>Experience with food quality systems such as SQF, HACCP, and GMPs.</li><li>HACCP certification.</li><li>Ability to drive continuous improvement and affect change through indirect leadership.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience in quality assurance specific to food manufacturing, particularly with chocolate products.</li><li>Strong interpersonal, communication, coaching, and conflict management skills.</li><li>Ability to write and implement policies and procedures.</li><li>Willingness to travel infrequently.</li></ul>Work EnvironmentThe position is based in a manufacturing and lab environment. The role offers an opportunity to join a quickly growing and innovative team.Job Type &amp; LocationThis is a Permanent position based out of Saint Louis, MO.Pay and BenefitsThe pay range for this position is $70000.00 - $90000.00/yr.Health &amp; Wellness
Medical, dental, and vision insurance

Health savings accounts (HSA) or flexible spending accounts (FSA)

Mental health support and employee assistance programs

Wellness programs, fitness reimbursements, or gym discounts

💼 Financial &amp; Retirement
Competitive salary and performance-based bonuses

401(k) or other retirement savings plans with employer match

Life and disability insurance

Commuter benefits or transportation stipendsWorkplace TypeThis is a fully onsite position in Saint Louis,MO.Application DeadlineThis position is anticipated to close on Feb 27, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

QA Supervisor

<h2>Key Responsibilities</h2><ul><li>Assist with production tasks such as measuring, weighing, and preparing raw materials.</li><li>Set up, operate, and assist with basic machine/equipment operation as needed.</li><li>Package and label finished goods accurately and efficiently.</li><li>Perform quality checks to ensure products meet company standards</li><li>Maintain a clean, organized, and safe work environment by following sanitation and safety procedures.</li><li>Monitor inventory levels and report when supplies need replenishment</li><li>Assist in loading/unloading materials and preparing products for shipment.</li><li>Communicate production issues or equipment concerns to supervisors promptly.</li></ul><hr><h2>Qualifications</h2><ul><li>High school diploma or equivalent required.</li><li>Prior experience in manufacturing or food production preferred but not required.</li><li>Ability to lift, stand, and perform physical tasks for extended periods.</li><li>Strong attention to detail and ability to follow instructions accurately.</li><li>Basic math and measurement skills.</li><li>Ability to work in a fast‑paced, team‑oriented environment.</li></ul><hr><h2>What We Offer</h2><ul><li>Competitive hourly pay</li><li>Overtime opportunities</li><li>Stable, long‑term career growth in food manufacturing</li><li>Training and advancement pathways</li><li>Health, dental, and other benefits </li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Clintonville, WI.Pay and BenefitsThe pay range for this position is $21.78 - $24.78/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Clintonville,WI.Application DeadlineThis position is anticipated to close on Feb 27, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

QA Tech

QA TechWe are seeking a dedicated QA Tech to join our team. You will support our quality department by contributing to and maintaining environmental monitoring compliance, regulatory protocols and ensuring the integrity of our environmental controls.Responsibilities<ul><li>Support the quality department with building qualifications and testing equipment.</li><li>Author reports to document and communicate results.</li><li>Conduct laboratory analysis and monitor microbial cultures and samples.</li><li>Investigate growth and characteristics of microscopic organisms such as bacteria, algae, and fungi.</li><li>Supervise and conduct research on microbiological activities.</li><li>Maintain knowledge of research methods and perform manual operations on supplies, surfaces, and materials.</li><li>Develop and maintain validation protocols for environmental controls.</li><li>Perform laboratory analysis on materials after sterilization.</li><li>Test component samples, identify contamination, and initiate corrective measures.</li><li>Study cultures of microorganisms and ensure control over moisture and temperature.</li><li>Monitor physiological and morphological characteristics to identify microorganisms.</li><li>Perform tests on incoming ingredients and document results.</li><li>Prepare research papers and documents for protocols.</li><li>Conduct audits on environmental programs and perform reviews.</li><li>Develop testing processes for raw materials and equipment.</li><li>Monitor finished products and investigate issues to prevent GMP problems.</li><li>Maintain accurate records and perform tests in the laboratory.</li><li>Develop and document microbiology laboratory processes and prepare final reports.</li><li>Maintain purchase orders for laboratory processes and monitor inventory.</li><li>Review product batch records and communicate issues with supervisors.</li><li>Prepare paperwork for shipping.</li><li>Implement new requirements and ensure compliance with the quality management system.</li><li>Maintain professional and technical knowledge through educational workshops and networking.</li><li>Contribute to team efforts by accomplishing related results as needed.</li><li>Take on additional responsibilities as directed by management.</li></ul>Essential Skills<ul><li>Quality control in-process and finished products</li><li>Process QC and document control</li><li>FDA and Tissue Processing</li><li>Cleanroom and aseptic technique</li><li>Environmental Monitoring</li><li>Microbiology and GMP knowledge</li></ul>Additional Skills &amp; Qualifications<ul><li>High School Diploma or equivalent</li><li>Minimum 2+ years of GMP experience in an aseptic environment (medical device/pharma)</li><li>Preferred: Quality control experience in ISO medical device manufacturing</li></ul>Work EnvironmentThe position is based in a biomedical manufacturing environment. You will work in a clean room laboratory and office setting. The role requires adherence to clean room protocols and a professional dress code.Job Type &amp; LocationThis is a Permanent position based out of Gainesville, FL.Pay and BenefitsThe pay range for this position is $20.00 - $20.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Gainesville,FL.Application DeadlineThis position is anticipated to close on Mar 4, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

<h2 style="text-align:center;">QA Technician (Spanish Speaking Required)</h2>﻿Job DescriptionEnsure the quality and safety of food products through comprehensive quality checks, auditing, and reporting. You will be responsible for sampling and testing incoming ingredients and packaging supplies, maintaining accurate records, and using lab equipment for quality tests. Additionally, you will conduct audits of finished products and production lines and communicate effectively with line leads and production supervisors regarding any quality issues.Responsibilities<ul><li>Verify food quality and food safety through quality checks, auditing, and reporting, including SQF, HACCP, and GMP.</li><li>Sample and test incoming ingredients and packaging supplies.</li><li>Maintain accurate records and results of quality assurance tests.</li><li>Use lab equipment to perform quality tests, including metal content, weight, and temperature checks.</li><li>Conduct audits of finished products and production lines.</li><li>Communicate effectively with Line Lead and Production Supervisor about packaging and quality issues.</li><li>Dispose of off-quality or improper product and materials in designated areas.</li><li>Conduct line inspections for cleanliness and perform visual quality checks of packaged and finished products.</li><li>Collect and retain samples needed for customers and micro samples.</li><li>Document product records in computer systems using MS Excel and Access.</li><li>Assist production in packing, boxing, and labeling finished products.</li></ul>Essential Skills<ul><li>Bilingual in Spanish and English with strong oral and written communication skills.</li><li>Basic computer skills, including Microsoft Word, Excel, and Outlook</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Saint Paul, MN.Pay and BenefitsThe pay range for this position is $21.00 - $25.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Saint Paul,MN.Application DeadlineThis position is anticipated to close on Feb 27, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

QA Tech (Spanish Speaking, Entry-Level 25/hr)

QA TechnicianJob DescriptionThe QA Technician will play a crucial role in ensuring the quality of products by reviewing batch records, identifying documentation errors, and coordinating with Operations to resolve issues. This role involves filing and document retrieval as needed, and requires excellent attention to detail, organizational skills, and interpersonal skills to ensure timely and accurate evaluation of documentation.Responsibilities<ul><li>Review production batch documentation for compliance with cGMP good documentation requirements.</li><li>Communicate effectively and coordinate tasks with Manufacturing and Quality Control to facilitate the timely release of products.</li><li>Process 100% inspection rework activities and stock adjustments.</li><li>Track and trend functional metrics.</li><li>Support compliance initiatives and Regulatory and Customer Audits.</li><li>Assist with continuous improvement projects and participate in lean activities.</li></ul>Essential Skills<ul><li>Quality assurance and document control expertise.</li><li>Working knowledge of computer software programs such as Teams and Excel.</li><li>Self-motivated and able to work in a team environment.</li><li>Ability to work in a filing room environment and lift 50 lbs for document archival, as needed.</li></ul>Additional Skills &amp; Qualifications<ul><li>1+ years of experience in QA, QC, or manufacturing within a regulated environment such as medical device, pharmaceutical, or food manufacturing.</li><li>Background in a Medical device, cGMP, or ISO certified environment.</li><li>Data entry skills and familiarity with inventory management systems such as SAP.</li><li>Proven ability to work effectively as a member of a cross-functional team.</li></ul>Job Type &amp; LocationThis is a Contract position based out of Lenexa, KS.Pay and BenefitsThe pay range for this position is $23.00 - $23.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Lenexa,KS.Application DeadlineThis position is anticipated to close on Mar 4, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

QA Technician

Job Title: QA TechnicianJob DescriptionThe QA Technician will play a crucial role in ensuring the quality of products by reviewing batch records, identifying documentation errors, and coordinating with Operations to resolve issues. This role involves filing and document retrieval as needed, and requires excellent attention to detail, organizational skills, and interpersonal skills to ensure timely and accurate evaluation of documentation.Responsibilities<ul><li>Review production batch documentation for compliance with cGMP good documentation requirements.</li><li>Communicate effectively and coordinate tasks with Manufacturing and Quality Control to facilitate the timely release of products.</li><li>Process 100% inspection rework activities and stock adjustments.</li><li>Track and trend functional metrics.</li><li>Support compliance initiatives and Regulatory and Customer Audits.</li><li>Assist with continuous improvement projects and participate in lean activities.</li></ul>Essential Skills<ul><li>Quality assurance and document control expertise.</li><li>Working knowledge of computer software programs such as Teams and Excel.</li><li>Self-motivated and able to work in a team environment.</li><li>Ability to work in a filing room environment and lift 50 lbs for document archival, as needed.</li></ul>Additional Skills &amp; Qualifications<ul><li>1+ years of experience in QA, QC, or manufacturing within a regulated environment such as medical device, pharmaceutical, or food manufacturing.</li><li>Background in a Medical device, cGMP, or ISO certified environment.</li><li>Data entry skills and familiarity with inventory management systems such as SAP.</li><li>Proven ability to work effectively as a member of a cross-functional team.</li></ul>Work EnvironmentThe role involves a long-term contract with working hours from Thursday to Sunday, 7am to 5:30pm. The position is not lab-based, focusing instead on documenting all QA activities. Work requires recurring bending, crouching, stretching, or reaching, and may frequently involve operating equipment, including a keyboard with a mouse. The environment is usually comfortable but does require time on the production floor to collect documentation. There is a frequent need to distinguish among or interpret a variety of sensory inputs that require attention to decode and identify.Job Type &amp; LocationThis is a Contract position based out of Lenexa, KS.Pay and BenefitsThe pay range for this position is $23.00 - $23.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Lenexa,KS.Application DeadlineThis position is anticipated to close on Mar 3, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

<h2>QA Technician</h2>Job DescriptionIn this role, you will play a critical part in protecting product quality and ensuring food safety across our production operations. The Food Safety &amp; Quality Assurance Technician is responsible for monitoring, verifying, and documenting key food safety and quality standards throughout the production process in a USDA- and FDA-regulated environment. This position is ideal for someone who is detail-oriented, quality-driven, and passionate about food safety and compliance.Responsibilities<ul><li>Support compliance and Quality Assurance activities within a USDA and FDA regulated facility.</li><li>Verify and support HACCP and PCQI programs, including accurate and timely documentation.</li><li>Perform environmental swabbing for ATP and APC testing related to pathogens such as Coliform and Salmonella (sample collection and data recording only; no laboratory testing required).</li><li>Conduct line checks every two hours, ensuring processes, programs, and food safety standards are being followed.</li><li>Validate that GMPs and food safety protocols are consistently met by production staff.</li><li>Maintain clear, accurate documentation to support audits, inspections, and internal quality programs.</li></ul>Additional Skills &amp; Qualifications<ul><li>High School Diploma or equivalent required.</li><li>Previous Quality or Food Safety experience in a food manufacturing environment is highly desired, but not required.</li><li>Familiarity with GMPs, food safety standards, and regulated environments preferred.</li><li>Bilingual skills are a plus.</li><li>Strong attention to detail with the ability to accurately document findings.</li><li>Comfortable working on the production floor and communicating with cross-functional teams.</li></ul>Work EnvironmentThis role reports directly to the QA Manager. The position is primarily based on the production floor within a cold storage manufacturing facility. The environment is maintained at approximately 30°F, and candidates should be comfortable working in cold conditions for extended periods. Production operates Sunday through Friday with Saturdays off, plus one additional weekday off. Start times vary daily between 3:30 AM and 12:00 PM. Employees work 8-hour shifts. Overtime is common, though the current workload is lighter and averaging 40 hours per week. Typically, a 3-week training process is involved. 70% of time is spent on the production floor performing spot checks and line checks, while 30% is dedicated to documentation and desk-based quality work.Job Type &amp; LocationThis is a Contract to Hire position based out of Saint Paul, MN.Pay and BenefitsThe pay range for this position is $19.00 - $19.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Saint Paul,MN.Application DeadlineThis position is anticipated to close on Feb 27, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Description
					Performs quality audit of the Facility, process including GMP
Support work order management 
Assist with micro prep, testing, and release of samples
Assist with routine support tasks (sampling, checks, documentation, etc.) as assigned by QA Supervisor
•	Follow GMP/GLP Guidelines
										Skills
					Food chemistry, Quality assurance, Qc, Qc testing, sample prep, media prep, food analysis testing, Food science, Biologics
										Top Skills Details
					Food chemistry,Quality assurance,Qc,Qc testing,sample prep,media prep
										Additional Skills &amp; Qualifications
					1-2 years of working in a food manufacturing environment
Associate's 0-1 years' experience of HS diploma with manufacturing/food manufacturing experience
										Experience Level
					Intermediate Level
					Job Type &amp; LocationThis is a Contract to Hire position based out of Ayer, MA.Pay and BenefitsThe pay range for this position is $20.00 - $20.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Ayer,MA.Application DeadlineThis position is anticipated to close on Mar 2, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

<h2 style="text-align:center;">QA Technician (Spanish Speaking Required)</h2>﻿Job DescriptionEnsure the quality and safety of food products through comprehensive quality checks, auditing, and reporting. You will be responsible for sampling and testing incoming ingredients and packaging supplies, maintaining accurate records, and using lab equipment for quality tests. Additionally, you will conduct audits of finished products and production lines and communicate effectively with line leads and production supervisors regarding any quality issues.Responsibilities<ul><li>Verify food quality and food safety through quality checks, auditing, and reporting, including SQF, HACCP, and GMP.</li><li>Sample and test incoming ingredients and packaging supplies.</li><li>Maintain accurate records and results of quality assurance tests.</li><li>Use lab equipment to perform quality tests, including metal content, weight, and temperature checks.</li><li>Conduct audits of finished products and production lines.</li><li>Communicate effectively with Line Lead and Production Supervisor about packaging and quality issues.</li><li>Dispose of off-quality or improper product and materials in designated areas.</li><li>Conduct line inspections for cleanliness and perform visual quality checks of packaged and finished products.</li><li>Collect and retain samples needed for customers and micro samples.</li><li>Document product records in computer systems using MS Excel and Access.</li><li>Assist production in packing, boxing, and labeling finished products.</li></ul>Essential Skills<ul><li>Bilingual in Spanish and English with strong oral and written communication skills.</li><li>Basic computer skills, including Microsoft Word, Excel, and Outlook</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Saint Paul, MN.Pay and BenefitsThe pay range for this position is $21.00 - $25.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Saint Paul,MN.Application DeadlineThis position is anticipated to close on Mar 6, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

<h2 style="text-align:center;">QA Technician (Spanish Speaking Required)</h2>﻿Job DescriptionEnsure the quality and safety of food products through comprehensive quality checks, auditing, and reporting. You will be responsible for sampling and testing incoming ingredients and packaging supplies, maintaining accurate records, and using lab equipment for quality tests. Additionally, you will conduct audits of finished products and production lines and communicate effectively with line leads and production supervisors regarding any quality issues.Responsibilities<ul><li>Verify food quality and food safety through quality checks, auditing, and reporting, including SQF, HACCP, and GMP.</li><li>Sample and test incoming ingredients and packaging supplies.</li><li>Maintain accurate records and results of quality assurance tests.</li><li>Use lab equipment to perform quality tests, including metal content, weight, and temperature checks.</li><li>Conduct audits of finished products and production lines.</li><li>Communicate effectively with Line Lead and Production Supervisor about packaging and quality issues.</li><li>Dispose of off-quality or improper product and materials in designated areas.</li><li>Conduct line inspections for cleanliness and perform visual quality checks of packaged and finished products.</li><li>Collect and retain samples needed for customers and micro samples.</li><li>Document product records in computer systems using MS Excel and Access.</li><li>Assist production in packing, boxing, and labeling finished products.</li></ul>Essential Skills<ul><li>Bilingual in Spanish and English with strong oral and written communication skills.</li><li>Basic computer skills, including Microsoft Word, Excel, and Outlook</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Saint Paul, MN.Pay and BenefitsThe pay range for this position is $21.00 - $25.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Saint Paul,MN.Application DeadlineThis position is anticipated to close on Feb 28, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

QA TechnicianJob DescriptionThe QA Technician will play a crucial role in ensuring the quality of products by reviewing batch records, identifying documentation errors, and coordinating with Operations to resolve issues. This role involves filing and document retrieval as needed, and requires excellent attention to detail, organizational skills, and interpersonal skills to ensure timely and accurate evaluation of documentation.Responsibilities<ul><li>Review production batch documentation for compliance with cGMP good documentation requirements.</li><li>Communicate effectively and coordinate tasks with Manufacturing and Quality Control to facilitate the timely release of products.</li><li>Process 100% inspection rework activities and stock adjustments.</li><li>Track and trend functional metrics.</li><li>Support compliance initiatives and Regulatory and Customer Audits.</li><li>Assist with continuous improvement projects and participate in lean activities.</li></ul>Essential Skills<ul><li>Quality assurance and document control expertise.</li><li>Working knowledge of computer software programs such as Teams and Excel.</li><li>Self-motivated and able to work in a team environment.</li><li>Ability to work in a filing room environment and lift 50 lbs for document archival, as needed.</li></ul>Additional Skills &amp; Qualifications<ul><li>1+ years of experience in QA, QC, or manufacturing within a regulated environment such as medical device, pharmaceutical, or food manufacturing.</li><li>Background in a Medical device, cGMP, or ISO certified environment.</li><li>Data entry skills and familiarity with inventory management systems such as SAP.</li><li>Proven ability to work effectively as a member of a cross-functional team.</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Lenexa, KS.Pay and BenefitsThe pay range for this position is $23.00 - $23.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Lenexa,KS.Application DeadlineThis position is anticipated to close on Feb 28, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Quality Assurance - GMP Document ControlJob DescriptionThe QA Technician will play a crucial role in ensuring the quality of products by reviewing batch records, identifying documentation errors, and coordinating with Operations to resolve issues. This role involves filing and document retrieval as needed, and requires excellent attention to detail, organizational skills, and interpersonal skills to ensure timely and accurate evaluation of documentation.Responsibilities<ul><li>Review production batch documentation for compliance with cGMP good documentation requirements.</li><li>Communicate effectively and coordinate tasks with Manufacturing and Quality Control to facilitate the timely release of products.</li><li>Process 100% inspection rework activities and stock adjustments.</li><li>Track and trend functional metrics.</li><li>Support compliance initiatives and Regulatory and Customer Audits.</li><li>Assist with continuous improvement projects and participate in lean activities.</li></ul>Essential Skills<ul><li>Quality assurance and document control expertise.</li><li>Working knowledge of computer software programs such as Teams and Excel.</li><li>Self-motivated and able to work in a team environment.</li><li>Ability to work in a filing room environment and lift 50 lbs for document archival, as needed.</li></ul>Additional Skills &amp; Qualifications<ul><li>1+ years of experience in QA, QC, or manufacturing within a regulated environment such as medical device, pharmaceutical, or food manufacturing.</li><li>Background in a Medical device, cGMP, or ISO certified environment.</li><li>Data entry skills and familiarity with inventory management systems such as SAP.</li><li>Proven ability to work effectively as a member of a cross-functional team.</li></ul>Job Type &amp; LocationThis is a Contract position based out of Lenexa, KS.Pay and BenefitsThe pay range for this position is $23.00 - $23.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Lenexa,KS.Application DeadlineThis position is anticipated to close on Mar 5, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

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