Description- Administer, manage, communicate, and update the company’s safety program- Collaborate with project managers, supervisors, and subcontractors to integrate safety into all aspects of construction activities.- Conduct jobsite and work area audits.- Attends planning, pre-job and project meetings to ensure safety concerns are being addressed and resolved.SkillsSafety, Safety management, ConstructionTop Skills DetailsSafety,Safety managementConstructionAdditional Skills &amp; Qualifications- 3-5 years of experience working in the commercial construction industry with safety experience with the proven ability to identify workable solutions to eliminate hazards.- Relevant safety certifications (e.g., OSHA certifications, CSP)Job Type &amp; LocationThis is a Permanent position based out of Westerville, OH.Pay and BenefitsThe pay range for this position is $65000.00 - $90000.00/yr.Full medical, dental, and vision insurance. Ability to contribute to 401k.Workplace TypeThis is a fully onsite position in Westerville,OH.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.

public

Safety Specialist

Job Title: Safety SpecialistJob DescriptionAs a Safety Specialist, you will be responsible for ensuring the safety, health, and environmental compliance onsite during installation and maintenance activities. You will collaborate with various stakeholders to solve problems, conduct audits, and investigate incidents while providing service-oriented support to employees, customers, and contractors. The role involves developing and implementing safety programs and training.Responsibilities<ul><li>Develop, review, evaluate, and implement health and safety policies, programs, and procedures.</li><li>Increase health and safety awareness at all organizational levels.</li><li>Investigate all serious and critical personal injury and near-miss incidents.</li><li>Assist with root cause analysis and solution identification for incident causal factors.</li><li>Respond to and track employees' safety concerns to completion.</li><li>Maintain records in compliance with regulatory requirements and prepare reports.</li><li>Provide direction to contract safety personnel.</li><li>Conduct worksite safety inspections and collaborate with employees and management to implement controls.</li><li>Assist in developing and managing site safety plans.</li><li>Coordinate and conduct on-site customer-specific safety training.</li><li>Conduct weekly safety audits and report findings.</li><li>Arrange for workplace safety evaluations by external agencies as needed.</li><li>Liaise with customer personnel and contracted personnel regarding safety procedures.</li><li>Develop and deliver assigned safety training programs.</li><li>Coordinate training in safety areas such as first aid, accident prevention, and workplace inspections.</li><li>Liaise with customers regarding emergency procedures and safety education programs.</li><li>Analyze work processes, perform risk assessments, and implement controls.</li><li>Act as a liaison with regulatory agencies as required.</li></ul>Essential Skills<ul><li>2+ years of EHS experience in a professional environment (manufacturing or construction).</li><li>Experience in creating safety plans (SOPs).</li><li>Experience in at least two professional safety audits.</li><li>General knowledge of accident investigation and root cause analysis.</li><li>Familiarity with OSHA regulatory requirements.</li><li>Strong communication skills.</li><li>Experience working with contractors and construction safety.</li><li>Ability to deliver and document training professionally.</li><li>Organizational abilities to manage multiple projects.</li><li>Strong writing skills for process documentation and report preparation.</li><li>Ability to work collaboratively as a team member.</li><li>Ability to exercise independent judgment and take initiative.</li></ul>Additional Skills &amp; Qualifications<ul><li>BCSP certification (CHST, OHST, ASP, GSP) preferred.</li></ul>Work EnvironmentThis role is onsite at TSMC, involving work in semiconductor clean room environments. The position operates Monday through Friday during the day shift. The dress code includes casual attire with provided PPE such as long pants, long sleeve shirts, hard hats, and safety glasses. The role requires up to 90% travel, primarily domestic with potential international travel. A clean driving record is essential. The company offers great long-term career growth, excellent benefits, and bonus programs.Job Type &amp; LocationThis is a Contract to Hire position based out of Chandler, AZ.Pay and BenefitsThe pay range for this position is $38.00 - $49.00/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 Chandler,AZ.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: Safety SpecialistJob DescriptionAs a Safety Specialist, you will be responsible for ensuring the safety, health, and environmental compliance onsite during installation and maintenance activities. You will collaborate with various stakeholders to solve problems, conduct audits, and investigate incidents while providing service-oriented support to employees, customers, and contractors. The role involves developing and implementing safety programs and training.Responsibilities<ul><li>Develop, review, evaluate, and implement health and safety policies, programs, and procedures.</li><li>Increase health and safety awareness at all organizational levels.</li><li>Investigate all serious and critical personal injury and near-miss incidents.</li><li>Assist with root cause analysis and solution identification for incident causal factors.</li><li>Respond to and track employees' safety concerns to completion.</li><li>Maintain records in compliance with regulatory requirements and prepare reports.</li><li>Provide direction to contract safety personnel.</li><li>Conduct worksite safety inspections and collaborate with employees and management to implement controls.</li><li>Assist in developing and managing site safety plans.</li><li>Coordinate and conduct on-site customer-specific safety training.</li><li>Conduct weekly safety audits and report findings.</li><li>Arrange for workplace safety evaluations by external agencies as needed.</li><li>Liaise with customer personnel and contracted personnel regarding safety procedures.</li><li>Develop and deliver assigned safety training programs.</li><li>Coordinate training in safety areas such as first aid, accident prevention, and workplace inspections.</li><li>Liaise with customers regarding emergency procedures and safety education programs.</li><li>Analyze work processes, perform risk assessments, and implement controls.</li><li>Act as a liaison with regulatory agencies as required.</li></ul>Essential Skills<ul><li>2+ years of EHS experience in a professional environment (manufacturing or construction).</li><li>Experience in creating safety plans (SOPs).</li><li>Experience in at least 2 professional safety audits.</li><li>General knowledge of accident investigation and root cause analysis.</li><li>Familiarity with OSHA regulatory requirements.</li></ul>Additional Skills &amp; Qualifications<ul><li>BCSP certification (CHST, OHST, ASP, GSP) preferred.</li><li>Strong communication skills.</li><li>Experience working with contractors and construction safety.</li><li>Ability to deliver and document training professionally.</li><li>Organizational abilities to manage multiple projects.</li><li>Strong writing skills for process documentation and report preparation.</li><li>Ability to work collaboratively as a team member.</li><li>Ability to exercise independent judgment and take initiative.</li></ul>Work EnvironmentThis role is onsite with semiconductor construction on the North side of Phoenix and will involve work in clean room environments. The position operates Monday through Friday during the day shift. The dress code includes casual attire with provided PPE such as long pants, long sleeve shirts, hard hats, and safety glasses. The role requires up to 90% travel, primarily domestic with potential international travel. A clean driving record is essential. The company offers great long-term career growth, excellent benefits, and bonus programs.Job Type &amp; LocationThis is a Contract to Hire position based out of Chandler, AZ.Pay and BenefitsThe pay range for this position is $38.00 - $49.00/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 Chandler,AZ.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: Safety Systems EngineerJob DescriptionWe are seeking a Safety Systems Engineer with a passion for ensuring flight safety and airworthiness. This role offers the opportunity to work on challenging projects that directly impact aviation safety in a fully remote setting. You will be part of a well-established engineering firm that specializes in safety-critical systems for the aviation industry.Responsibilities<ul><li>Perform system and aircraft-level safety assessments in accordance with ARP4761 / ARP4761A.</li><li>Develop and maintain safety artifacts, including Functional Hazard Assessments (FHA / AFHA), Fault Tree Analyses (FTA), Common Cause Analyses (CCA / CMA), and System Safety Assessments (SSA).</li><li>Support safety aspect derivation and allocation to system and subsystem requirements.</li><li>Collaborate with systems, software, hardware, and certification engineers to ensure safety objectives are correctly implemented.</li><li>Provide safety analysis support for Part 23 aircraft and general aviation avionics systems.</li><li>Participate in design reviews to evaluate safety impacts of architectural and functional changes.</li><li>Support certification audits and data generation activities as required.</li></ul>Essential Skills<ul><li>Performing safety assessments under ARP4761 with at least 3 years of strong hands-on experience.</li><li>Experience creating FTA, CMA, and SSA deliverables.</li><li>Experience in aviation or aerospace systems safety engineering.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience supporting Part 23 aircraft programs or general aviation platforms.</li><li>Experience working with FAA or EASA certification projects.</li><li>Prior exposure to avionics, flight controls, propulsion, or aircraft systems safety.</li><li>Comfortable working in distributed, remote engineering teams.</li></ul>Work EnvironmentThis is a fully remote position. You will be provided with a home setup to support your work. You will have the flexibility to work from anywhere, contributing to general aviation programs and making a deep technical contribution to system and aircraft safety.Job Type &amp; LocationThis is a Contract position based out of Phoenix, AZ.Pay and BenefitsThe pay range for this position is $110000.00 - $130000.00/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 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.

Safety Systems Engineer

Job Title: Sales EngineerJob DescriptionThe primary focus of this role is maintaining and supporting existing accounts, with an active role in identifying and developing new business opportunities.Responsibilities<ul><li>Provide technical support to customers and internal teams regarding custom hydraulic cylinder applications.</li><li>Assist the sales department in preparing accurate and competitive quotes for custom-designed hydraulic cylinders tailored to customer-specific applications.</li><li>Interpret technical drawings and specifications to ensure accurate pricing and feasibility of manufacturing.</li><li>Proactively research and identify potential customers and market segments that align with the company’s capabilities and product offerings.</li><li>Follow up on sales leads and inquiries with a technical, solutions-based approach.</li><li>Build new customer relationships through calls, emails, and virtual/in-person meetings.</li><li>Work with the Quality Assurance department to evaluate and process customer returns (RGA’s), identifying root causes and implementing corrective actions where necessary.</li><li>Communicate with customers to resolve technical issues related to returned products.</li><li>Collaborate closely with the engineering team and shop floor personnel to ensure production requirements meet customer expectations and design parameters.</li><li>Provide internal engineering assistance, including 2D/3D documentation, design modifications, and technical validation of components.</li><li>Maintain thorough and accurate records of customer communications, quote status, product modifications, and engineering support.</li><li>Assist in preparing technical documentation and product literature as needed for internal and customer use.</li></ul>Essential Skills<ul><li>Minimum of 3 years of experience in inside sales, technical sales, or applications engineering within the fluid power or hydraulics industry.</li><li>Minimum 2 years of experience and understanding of hydraulic systems, including pressure and tonnage calculations, cylinder sizing, and pump performance.</li><li>Ability to read and interpret mechanical drawings and hydraulic schematics.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience around ERP systems is a plus.</li></ul>Work EnvironmentInitially, the role involves maintaining current accounts, transitioning to prospecting for new business opportunities. The work environment fosters collaboration with engineering and shop floor personnel to meet customer expectations.Job Type &amp; LocationThis is a Permanent position based out of New Berlin, WI.Pay and BenefitsThe pay range for this position is $90000.00 - $100000.00/yr.Family owned business -medical, dental, vision, 401KWorkplace TypeThis is a fully onsite position in New Berlin,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.

Sales Engineer

Job Title: Sales EngineerJob DescriptionThe primary focus of this role is maintaining and supporting existing accounts, with an active role in identifying and developing new business opportunities.Responsibilities<ul><li>Provide technical support to customers and internal teams regarding custom hydraulic cylinder applications.</li><li>Assist the sales department in preparing accurate and competitive quotes for custom-designed hydraulic cylinders tailored to customer-specific applications.</li><li>Interpret technical drawings and specifications to ensure accurate pricing and feasibility of manufacturing.</li><li>Proactively research and identify potential customers and market segments that align with the company’s capabilities and product offerings.</li><li>Follow up on sales leads and inquiries with a technical, solutions-based approach.</li><li>Build new customer relationships through calls, emails, and virtual/in-person meetings.</li><li>Work with the Quality Assurance department to evaluate and process customer returns (RGA’s), identifying root causes and implementing corrective actions where necessary.</li><li>Communicate with customers to resolve technical issues related to returned products.</li><li>Collaborate closely with the engineering team and shop floor personnel to ensure production requirements meet customer expectations and design parameters.</li><li>Provide internal engineering assistance, including 2D/3D documentation, design modifications, and technical validation of components.</li><li>Maintain thorough and accurate records of customer communications, quote status, product modifications, and engineering support.</li><li>Assist in preparing technical documentation and product literature as needed for internal and customer use.</li></ul>Essential Skills<ul><li>Minimum of 3 years of experience in inside sales, technical sales, or applications engineering within the fluid power or hydraulics industry.</li><li>Minimum 2 years of experience and understanding of hydraulic systems, including pressure and tonnage calculations, cylinder sizing, and pump performance.</li><li>Ability to read and interpret mechanical drawings and hydraulic schematics.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience around ERP systems is a plus.</li></ul>Work EnvironmentInitially, the role involves maintaining current accounts, transitioning to prospecting for new business opportunities. The work environment fosters collaboration with engineering and shop floor personnel to meet customer expectations.Job Type &amp; LocationThis is a Permanent position based out of New Berlin, WI.Pay and BenefitsThe pay range for this position is $90000.00 - $100000.00/yr.Family owned business -medical, dental, vision, 401KWorkplace TypeThis is a fully onsite position in New Berlin,WI.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: Sales EngineerJob DescriptionThe Sales Engineer is responsible for driving sales and effectively communicating with customers. This role involves enhancing customer satisfaction, supporting project meetings, and maintaining overall sales performance.Responsibilities<ul><li>Achieve departmental business plan objectives.</li><li>Ensure compliance with existing quality systems such as TS and ISO.</li><li>Enhance customer satisfaction expectations.</li><li>Support project and PEM meetings as required.</li><li>Maintain sales activities with assigned customers.</li><li>Develop and sustain new business with current and new customers.</li><li>Conduct customer visitations and presentations.</li><li>Communicate customer requirements with other departments.</li><li>Collect and document market data related to competitor products and market trends.</li><li>Create and modify company marketing/sales strategies.</li><li>Develop sales forecasts, cost analyses, and regulatory reports.</li></ul>Essential Skills<ul><li>Bachelor's degree in Engineering.</li><li>Strong written and verbal communication skills.</li><li>Manufacturing engineering experience.</li><li>Continuous improvement experience.</li><li>Presentation skills.</li><li>Mechanical aptitude.</li><li>Experience with creo and lean manufacturing.</li><li>Sales experience.</li></ul>Additional Skills &amp; Qualifications<ul><li>Automotive sales experience preferred.</li><li>Knowledge of TPS is advantageous.</li><li>Familiarity with TS or ISO standards.</li></ul>Work EnvironmentThe work environment is a fast-paced automotive setting, involving collaboration with a team of experienced engineers. Standard work hours are from 8 AM to 5 PM, within an assembly environment. Employees benefit from good tenure and opportunities to work on new program launches.Job Type &amp; LocationThis is a Contract to Hire position based out of Lebanon, KY.Pay and BenefitsThe pay range for this position is $33.65 - $36.00/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 Lebanon,KY.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: Sales EngineerJob DescriptionWe are seeking a dynamic Sales Engineer to join our team. This role involves responding to and generating Requests for Quotations (RFQs), presenting technical details to customers, and negotiating effectively. The primary focus is on cables, wiring, and audio components. Responsibilities<ul><li>Manage and maintain relationships with customers worldwide.</li><li>Conduct regular customer visits and manage customer interactions.</li><li>Collect and analyze necessary information from customers, including model planning and strategy.</li><li>Participate in customer visits, Kick Off Meetings, and audits.</li><li>Handle all commercial issues from daily business operations.</li><li>Support RFQ, development, tooling, and sample cost negotiation within approved conditions.</li><li>Manage RFQ and offer processes according to internal procedures.</li><li>Prepare RFQ packages and initiate the RFQ process.</li><li>Support the entire RFQ process, including technical information management.</li><li>Develop business opportunities with customers.</li><li>Maintain price lists and program life cycle dates.</li><li>Analyze portfolio information and automotive technical trends.</li><li>Manage customer contract distribution and approval.</li></ul>Essential Skills<ul><li>10 years of experience in technical sales within the automotive industry.</li><li>Experience with electrical components, such as wire harnesses, cables, and audio components.</li><li>Proven experience in responding to technical RFQs and managing them.</li><li>Strong negotiation skills with customers.</li><li>Experience in managing existing business and developing new opportunities.</li><li>Ability to communicate effectively with internal departments and external customers.</li><li>High initiative and ability to complete tasks independently.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience in technical sales with Ford and/or GM is advantageous.</li><li>Previous experience working as an engineer is beneficial.</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Orion, MI.Pay and BenefitsThe pay range for this position is $45.00 - $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 Orion,MI.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.

Sales Engineer - Monee, IL﻿Responsibilities<ul><li>Manage customer requests via phone, email, and Web Shop, ensuring accuracy in handling.</li><li>Verify customer information and conduct parts research using SAP, equipment PDFs, and email correspondence with pictures to ensure correct orders.</li><li>Validate information and create quotes to share with customers.</li><li>Collect purchase orders (POs) and communicate order details and shipping expectations to customers.</li><li>Update internal systems (MRP/CRM/SAP) with accurate lead times.</li><li>Report suggestions, customer feedback, and operational issues to the Commercial Team Lead.</li><li>Proactively upsell and cross-sell relevant products based on customer interests and buying behavior.</li><li>Maintain and update accurate part details, including part numbers, descriptions, specifications, and vendor information.</li><li>Update pricing and part details such as part numbers and descriptions.</li><li>Perform additional tasks related to troubleshooting, service, design, electrical, field service, mechanical, engineering, customer service, technical sales, and sales engineering.</li></ul>Essential Skills<ul><li>Ability to read schematics.</li><li>Experience in working with equipment, both electrically and mechanically.</li><li>Experience in phone and email customer service tied into hands-on engineering.</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Monee, IL.Pay and BenefitsThe pay range for this position is $20.00 - $28.50/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 Monee,IL.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.

<h2>Job Title: Sales Engineer</h2>Client is unable to provide visa sponsorship now or in the future. Job DescriptionThe Sales Engineer is responsible for driving sales and effectively communicating with customers. This role involves enhancing customer satisfaction, supporting project meetings, and maintaining overall sales performance.Responsibilities<ul><li>Achieve departmental business plan objectives.</li><li>Ensure compliance with existing quality systems such as TS and ISO.</li><li>Enhance customer satisfaction expectations.</li><li>Support project and PEM meetings as required.</li><li>Maintain sales activities with assigned customers.</li><li>Develop and sustain new business with current and new customers.</li><li>Conduct customer visitations and presentations.</li><li>Communicate customer requirements with other departments.</li><li>Collect and document market data related to competitor products and market trends.</li><li>Create and modify company marketing/sales strategies.</li><li>Develop sales forecasts, cost analyses, and regulatory reports.</li></ul>Essential Skills<ul><li>Bachelor's degree in Engineering.</li><li>Strong written and verbal communication skills.</li><li>Manufacturing engineering experience.</li><li>Continuous improvement experience.</li><li>Presentation skills.</li><li>Mechanical aptitude.</li><li>Experience with creo and lean manufacturing.</li><li>Sales experience.</li></ul>Additional Skills &amp; Qualifications<ul><li>Automotive sales experience preferred.</li><li>Knowledge of TPS is advantageous.</li><li>Familiarity with TS or ISO standards.</li></ul>Work EnvironmentThe work environment is a fast-paced automotive setting, involving collaboration with a team of experienced engineers. Standard work hours are from 8 AM to 5 PM, within an assembly environment. Employees benefit from good tenure and opportunities to work on new program launches.Job Type &amp; LocationThis is a Contract to Hire position based out of Lebanon, KY.Pay and BenefitsThe pay range for this position is $33.65 - $36.00/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 Lebanon,KY.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: Sales EngineerJob DescriptionThe Sales &amp; Estimating Engineer is a customer-facing technical lead responsible for managing the front end of the opportunity pipeline. This includes everything from RFQ intake and qualification through cost modeling, proposal creation, and handoff to production. The role blends applications engineering with consultative selling to secure profitable work aligned with metal spinning, sheet hydroforming, complex machining, laser cutting, and welding capabilities. The engineer ensures that estimates reflect quality systems and special process controls.Responsibilities<ul><li>Lead technical discussions on the manufacturability of exotic alloy components such as ducts, shrouds, heat shields, manifolds, and housings formed via metal spinning and hydroforming, with laser trimming as needed.</li><li>Prepare customer presentations and quotations that articulate the company's certifications, process controls, and value proposition.</li><li>Translate drawings, models, and specifications into costed routings covering materials, tooling/fixturing, forming, machining, laser cutting, welding, inspection, and logistics.</li><li>Build pricing models that incorporate cycle times, yields for exotic alloys, setup, run labor, special process compliance, and risk/contingency.</li><li>Draft clear statements of work and commercial terms, ensuring alignment with customer specifications and quality certifications.</li><li>Lead cross-functional kickoff meetings from award through engineering release, partnering with R&amp;D/prototyping, production, and quality teams.</li><li>Maintain visibility on quotes, orders, and delivery commitments using an operations approach.</li><li>Capture pricing and actuals feedback to continuously refine estimating accuracy and margin performance.</li><li>Maintain CRM discipline and drive quarterly bookings and margin targets.</li><li>Monitor market trends in super alloys/exotic metals and recommend campaigns and target accounts.</li></ul>Essential Skills<ul><li>Bachelor’s degree in Mechanical or Aerospace Engineering, or equivalent technical experience.</li><li>Experience with estimating, applications engineering, or technical sales within precision metal fabrication/forming or machining in the aerospace/defense industry.</li><li>Hands-on experience with manufacturing and fabrication processes.</li><li>Ability to read GD&amp;T prints; competence with CAD/CAM or cost-modeling tools.</li><li>Working knowledge of AS9100 and NADCAP requirements and their impact on estimating and production planning.</li><li>Strong commercial acumen: margin analysis, price-to-win strategies, and value-based proposals.</li><li>Excellent communication and customer engagement skills.</li><li>Experience with AS9100 and 5+ years of technical sales and estimating experience.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience with sales and estimating supporting companies like GE Aerospace, Rolls Royce, Pratt &amp; Whitney.</li><li>Familiarity with metal spinning, sheet hydroforming, multi-axis machining, laser cutting, and welding processes, including constraints of exotic alloys.</li></ul>Work Environment<ul><li>This role is within a small company with family values experiencing strong growth. </li><li>As the sole sales and estimating engineer on staff, you will work closely with the President and own efforts related to sales and estimating. </li><li>The company, consisting of 35 employees, is seeing increased orders from customers due to its success. </li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Brazil, IN.Pay and BenefitsThe pay range for this position is $48.07 - $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 fully onsite position in Brazil,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: Sales RepresentativeJob DescriptionAs a Sales Representative, you will maintain ongoing communication with current clients, proactively reaching out to understand their plumbing or water-related concerns and recommending appropriate solutions. You will use company pricing tools and insurance parameters to prepare accurate, competitive estimates for repairs or replacements, guiding customers toward the best option and securing sales. Serving as a knowledgeable point of contact, you will offer clear and reliable information to help customers make informed decisions. You will also utilize prospecting tools to follow up on leads for residential and commercial clients experiencing water damage or plumbing issues.Responsibilities<ul><li>Identify opportunities to repair or replace sewer lines for both residential and commercial properties.</li><li>Perform video inspections of sewer systems to evaluate issues such as root intrusion, structural damage, or other conditions requiring excavation or line replacement.</li><li>Present solutions for addressing water-related property damage in homes and businesses.</li><li>Conduct on-site evaluations to measure moisture levels, determine the extent of damage, and assess necessary restoration steps such as demolition or drying.</li></ul>Essential Skills<ul><li>Minimum of 2 years of customer interfacing sales experience.</li><li>Ability to articulate sales information effectively.</li><li>High level of awareness and ability to communicate clearly with homeowners and insurance adjusters.</li><li>Eagerness, upbeat attitude, and self-motivation.</li><li>Sales discipline, resilience, and ability to learn on the fly.</li><li>Results-oriented with a drive and competitive fire.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience in water restoration and excavation is advantageous.</li><li>Certifications in water restoration are beneficial.</li><li>No specific educational requirements.</li></ul>Work EnvironmentThe role involves working across San Bernardino, Riverside, and Orange counties, with a focus on areas such as Monrovia and Duarte. Candidates should be open to working nights and weekends, as these are the busiest times. Regular team meetings are held, sometimes requiring in-person attendance at least once a month. Training is hands-on, with a duration of 3-4 weeks, and involves modules specific to water restoration. Company vehicles are provided for excavation roles, while personal vehicles are used for water restoration, reimbursed at $0.725 per mile. An HIS License through the state of CA is required, with the company covering the fee and application process. Certifications in water restoration are expected within the first 6 months.Job Type &amp; LocationThis is a Permanent position based out of Corona, CA.Pay and BenefitsThe pay range for this position is $26000.00 - $100000.00/yr.Company Benefits
Medical insurance with a Prescription Drug Card
Accident and Critical Illness Insurance
Dental Insurance
Vision Insurance
Paid Vacation
Paid Training
Life Insurance
Matching 401K Retirement Savings Plan
Tuition Reimbursement
Profit SharingWorkplace TypeThis is a hybrid position in Corona,CA.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.

Sales Representative

Job Title: Sales RepresentativeJob DescriptionMaintain ongoing communication with current clients, reaching out proactively to understand their plumbing or water-related concerns and recommend appropriate solutions. Use company pricing tools and insurance parameters to prepare accurate, competitive estimates for repairs or replacements, guiding customers toward the best option and securing the sale. Serve as a knowledgeable point of contact, offering clear and reliable information to help customers make informed decisions. Utilize prospecting tools to follow up on leads for residential and commercial clients experiencing water damage or plumbing issues.Responsibilities<ul><li>Identify opportunities to repair or replace sewer lines for residential and commercial properties.</li><li>Perform video inspections of sewer systems to evaluate issues such as root intrusion, structural damage, or other conditions requiring excavation or line replacement.</li><li>Identify and present solutions for addressing water-related property damage in homes and businesses.</li><li>Conduct on-site evaluations to measure moisture levels, determine the extent of damage, and assess the necessity for demolition, drying, or other restoration steps.</li></ul>Essential Skills<ul><li>Experience in outside sales, preferably 6 months to 1 year in customer-facing roles.</li><li>Eagerness and self-motivation with a strong customer service orientation.</li></ul>Additional Skills &amp; Qualifications<ul><li>Clean and valid driver's license is mandatory.</li><li>Stability in career path, with a preference for those with customer-facing sales experience.</li><li>Background in construction, roofing, or home remodeling is beneficial.</li><li>Willingness to work additional shifts, including weekends.</li></ul>Work EnvironmentThis role involves working as a Field Supervisor for the Water Restoration and Excavation teams, covering Alameda County, Contra Costa County, and parts of San Joaquin County. Employees have the flexibility to start their day from home and are expected to be in the service area at the start of their shifts. Shifts vary, including 9am – 5pm, mid-shift 11am – 8pm, and 2pm – 10pm, with the possibility of longer days for Water Restoration roles. Weekend work may be required. Employees in excavation receive a company vehicle, while those in water restoration use personal vehicles with mileage reimbursement. Training is provided and lasts 4-6 weeks. The work environment is commission-based with uncapped potential, and there are incentives such as the Diamond Club for achieving sales targets.Job Type &amp; LocationThis is a Permanent position based out of Tracy, CA 95376.Pay and BenefitsThe pay range for this position is $26000.00 - $52000.00/yr.Medical insurance with a Prescription Drug Card
Accident and Critical Illness Insurance
Dental Insurance
Vision Insurance
Paid Vacation
Paid Training
Life Insurance
Matching 401K Retirement Savings Plan
Tuition Reimbursement
Profit SharingWorkplace TypeThis is a hybrid position in Tracy,CA 95376.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.

Sales Representative - Base Pay + Uncapped Commission

Sample Prep Technician - 2nd shift (2-10:30pm)Job DescriptionJoin a dynamic team in a fast-paced food laboratory environment as a Sample Prep Technician. This role involves supporting the preparation staff by labeling containers, washing glassware, and transporting samples. The position offers the opportunity for cross-training and advancement within the lab setting, with the possibility of transitioning into lab positions after a year.Responsibilities<ul><li>Assist in labeling and storing samples.</li><li>Reduce samples to powder or liquid form using liquid nitrogen.</li><li>Maintain strong documentation and adhere to company regulations.</li><li>Stand for the majority of the day and use a 5lb hammer to grind samples.</li><li>Work in specialty areas such as vessel washing and data entry.</li><li>Be flexible to work an average of 5 hours of overtime per week based on workload.</li></ul>Essential Skills<ul><li>High attention to detail and documentation.</li><li>Ability to work independently and reliability verified through references.</li><li>1+ years of experience with Microsoft Word and Excel.</li><li>Experience working under Good Laboratory Practice (GLP) regulations.</li></ul>Additional Skills &amp; Qualifications<ul><li>Associate's degree in Biotechnology with 2 years of industry lab experience, or</li><li>High School diploma with 3-4+ years of repetitive work experience and ability to lift 40-50 lbs.</li><li>Backgrounds in restaurant/cooking, pharmacy tech, landscaping, delivery driving, or assembly line work are beneficial.</li></ul>Work EnvironmentWork in a loud but fun prep lab environment where teamwork is key. The lab has recently moved to a new location to accommodate growth, and the Sample Prep team is experiencing a 20% increase in test production. The environment is fast-paced, similar to production work, with numerous promotional opportunities available. The team consists of 12-15 employees on the first and second shifts.Job Type &amp; LocationThis is a Contract to Hire position based out of Madison, WI.Pay and BenefitsThe pay range for this position is $20.17 - $20.17/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 Madison,WI.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.

Sample Prep Technician

<h1>Plant Hygiene &amp; Sanitation Manager – Job Description</h1><h2>Overview</h2>The Plant Hygiene &amp; Sanitation Manager leads all sanitation, hygiene, and environmental control programs within a food manufacturing facility. This role ensures that cleaning and sanitation systems effectively control microbiological, chemical, and physical hazards to protect food safety, product quality, and regulatory compliance. The position provides technical and scientific oversight of sanitation chemistry, environmental monitoring, and hygienic design while developing a high‑performing sanitation team and maintaining audit‑ready standards.<h2></h2><h2>Key Responsibilities</h2><h3>Sanitation &amp; Hygiene Program Leadership</h3><ul><li>Design, implement, and maintain sanitation and hygiene programs aligned with the facility’s Food Safety Management System (FSMS) and hazard control strategies.</li><li>Validate and verify sanitation procedures to ensure effective control of pathogenic and spoilage microorganisms.</li><li>Oversee sanitation of production equipment, processing lines, utilities, and facility infrastructure to prevent cross‑contamination and environmental risks.</li><li>Conduct sanitation verification through visual inspection, ATP testing, microbiological sampling, and chemical concentration checks.</li></ul><h3>Technical Expertise &amp; Environmental Control</h3><ul><li>Provide scientific oversight of cleaning and sanitizing chemicals, including detergents, acids, alkalis, oxidizers, and disinfectants.</li><li>Ensure proper chemical selection, dilution, application, storage, and disposal in accordance with SDS, regulatory standards, and environmental requirements.</li><li>Support and enhance environmental monitoring programs, including zone‑based sampling, trending, and risk‑based improvements.</li><li>Partner with chemical suppliers and internal teams to optimize sanitation chemistry for efficacy, material compatibility, and cost efficiency.</li></ul><h3>Regulatory Compliance &amp; Audit Readiness</h3><ul><li>Ensure sanitation and hygiene programs meet GMPs, FSMA Preventive Controls, and all applicable federal, state, and local regulations.</li><li>Support compliance with environmental, wastewater, and chemical discharge requirements.</li><li>Maintain audit‑ready documentation and support internal audits, third‑party food safety audits, and regulatory inspections.</li><li>Lead investigations of sanitation‑related deviations, root cause analysis, and corrective/preventive actions.</li></ul><h3>Leadership &amp; Cross‑Functional Collaboration</h3><ul><li>Lead, train, and develop sanitation personnel with a focus on food safety, hygiene science, and safe chemical handling.</li><li>Coordinate sanitation schedules with Production, Quality, Maintenance, and Engineering to support operational efficiency and hygienic design principles.</li><li>Promote a culture of food safety, scientific discipline, accountability, and continuous improvement.</li><li>Drive sanitation‑related continuous improvement initiatives using data, trend analysis, and risk‑based decision making.</li></ul><h3>Documentation &amp; Data Management</h3><ul><li>Maintain accurate sanitation records, logs, validation data, and verification documentation.</li><li>Review and trend sanitation, environmental, and microbiological data to assess program effectiveness.</li><li>Ensure sanitation procedures, work instructions, and training materials remain current and aligned with food safety requirements.</li></ul><h2>Essential Skills &amp; Experience</h2><ul><li>5–10 years of sanitation experience in food or beverage manufacturing.</li><li>Minimum 2–3 years in a supervisory or management role.</li><li>Experience managing downtime, operational priorities, and sanitation activities around production schedules.</li><li>Demonstrated success leading corrective actions, continuous improvement, and sanitation investigations.</li><li>Strong communication, leadership, and training capabilities.</li><li>Ability to interpret scientific data and apply findings to sanitation and food safety improvements.</li></ul><h2>Preferred Qualifications</h2><ul><li>Bachelor’s degree in Food Science, Microbiology, Environmental Science, or related field.</li><li>Relevant certifications strongly preferred: HACCP, SQF Practitioner, AIB, GMP, CIP, OSHA; PCQI a plus.</li><li>Proven sanitation leadership experience in a food or beverage manufacturing environment.</li><li>Strong understanding of microbial control, sanitation chemistry, and hygienic manufacturing principles.</li><li>Experience with environmental monitoring, allergen controls, and sanitation verification methods.</li><li>Working knowledge of GMPs, FSMA, HACCP-based systems, and audit expectations.</li><li>High attention to detail and strong problem‑solving skills.</li><li>Ability to make sound decisions in a regulated, high‑risk manufacturing environment.</li><li>Commitment to continuous improvement and professional development in food safety and sanitation science.</li></ul><h2>Work Environment</h2>This role operates within a manufacturing environment with exposure to water, chemicals, and varying temperatures. Use of personal protective equipment is required. The position may require flexible scheduling and support for off‑shift sanitation activities.Job Type &amp; LocationThis is a Permanent position based out of Memphis, TN.Pay and BenefitsThe pay range for this position is $73958.00 - $122031.00/yr.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 Memphis,TN.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.

Sanitation Manager

<h2 style="text-align:center;">Sanitation Technician</h2>Job DescriptionEnsuring compliance with hygiene and safety standards through meticulous sample collection and manual audits. You will prepare reagent solutions, document audit findings, and report to the appropriate health authorities. Additionally, you will maintain accurate records through data entry and report preparation, while supporting safety initiatives alongside the Safety &amp; Occupational Health team.Responsibilities<ul><li>Conduct sample collection and perform manual audits to ensure compliance with hygiene and safety standards.</li><li>Prepare reagent solutions for manual audits.</li><li>Document audit findings accurately and promptly, reporting to the Minnesota Department of Health.</li><li>Perform accurate documentation, including filing, data entry, and report preparation.</li><li>Maintain a clean and organized work environment through housekeeping duties.</li><li>Collaborate with the Safety &amp; Occupational Health team to support various initiatives and projects.</li><li>Adhere to company policies and procedures related to safety and hygiene.</li></ul>Skills &amp; Qualifications<ul><li>High school diploma minimum</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Eagan, MN.Pay and BenefitsThe pay range for this position is $22.00 - $22.00/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 Eagan,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.

Sanitation Technician

Job Title: Sanitation TechnicianJob DescriptionThe Sanitation Technician operates within safety and quality standards, adhering to good manufacturing practices (GMPs) and company policies and procedures. The role requires ensuring the use of proper personal protective equipment (PPE) and meeting quality standards for sanitation, including chemical concentrations, time and temperature, cleaning times, and flow rate. The technician monitors the C.I.P. operation, ensuring cleaning is completed to specifications and documented, while effectively communicating with management regarding equipment, food safety, quality, and sanitation issues.Responsibilities<ul><li>Monitor and document C.I.P. operations to ensure cleaning meets specifications.</li><li>Communicate effectively with management about equipment, food safety, quality, and sanitation issues.</li><li>Assist in inventory of chemicals, cleaning supplies, and parts.</li><li>Inspect sanitation work and follow up to ensure all standards are met for a safe start of production.</li><li>Meet expectations and results set for the position.</li><li>Perform other duties and responsibilities as assigned.</li></ul>Essential Skills<ul><li>Experience with GMP, sanitation, food safety, HACCP, and FDA regulations.</li><li>1-2 years of previous sanitation experience, preferably in the Food and Beverage industry.</li><li>Ability to comply with Quality Management and Food Safety Management requirements.</li><li>Effective communication skills in English, both verbal and written.</li><li>Ability to prioritize workload and adapt to shifts in daily priorities.</li><li>High attention to detail and a sense of urgency in addressing problems.</li><li>Basic math skills including addition, subtraction, multiplication, division, and averages.</li><li>Strong interpersonal skills fostering trust, accountability, collaboration, and teamwork.</li><li>Completion of Food Safety Training (Qualified Individual).</li></ul>Additional Skills &amp; Qualifications<ul><li>High school diploma or equivalent required.</li><li>Ability to work overtime as needed.</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Random Lake, WI.Pay and BenefitsThe pay range for this position is $26.50 - $27.00/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 Random Lake,WI.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 style="text-align:center;">Sanitation Technician</h2>Job DescriptionEnsuring compliance with hygiene and safety standards through meticulous sample collection and manual audits. You will prepare reagent solutions, document audit findings, and report to the appropriate health authorities. Additionally, you will maintain accurate records through data entry and report preparation, while supporting safety initiatives alongside the Safety &amp; Occupational Health team.Responsibilities<ul><li>Conduct sample collection and perform manual audits to ensure compliance with hygiene and safety standards.</li><li>Prepare reagent solutions for manual audits.</li><li>Document audit findings accurately and promptly, reporting to the Minnesota Department of Health.</li><li>Perform accurate documentation, including filing, data entry, and report preparation.</li><li>Maintain a clean and organized work environment through housekeeping duties.</li><li>Collaborate with the Safety &amp; Occupational Health team to support various initiatives and projects.</li><li>Adhere to company policies and procedures related to safety and hygiene.</li></ul>Skills &amp; Qualifications<ul><li>High school diploma minimum</li></ul>Job Type &amp; LocationThis is a Contract position based out of Eagan, MN.Pay and BenefitsThe pay range for this position is $22.00 - $22.00/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 Eagan,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.

Sterilization AssociateJob DescriptionAs a Data Collection Associate, you will conduct sample collection and perform manual audits to ensure compliance with hygiene and safety standards. You will prepare reagent solutions for manual audits, accurately report and document audit findings, and perform data entry and report preparation. Additionally, you will support housekeeping duties to maintain a clean and organized environment and collaborate with the Safety &amp; Occupational Health team on various projects.Responsibilities<ul><li>Conduct sample collection and perform manual audits in compliance with hygiene and safety standards.</li><li>Prepare reagent solutions for manual audits.</li><li>Report and document audit findings accurately and promptly.</li><li>Perform accurate documentation, filing, data entry, and report preparation.</li><li>Maintain a clean and organized work environment through housekeeping duties.</li><li>Collaborate with the Safety &amp; Occupational Health team to support initiatives and projects.</li><li>Adhere to all company policies and procedures related to safety and hygiene.</li></ul>Additional Skills &amp; Qualifications<ul><li>High school diploma minimum</li><li>Strong attention to detail and organizational skills</li><li>Ability to work independently and as part of a team</li></ul>Work EnvironmentThis is an office-based role with a 4 on-4 off schedule from 6am to 6pm. Also have a 4 on-4off schedule night shift 6pm to 6amJob Type &amp; LocationThis is a Contract position based out of Eagan, MN.Pay and BenefitsThe pay range for this position is $21.00 - $21.00/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 Eagan,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.

<h1>Job Title: Scheduler</h1><h2>Job Description</h2>We are seeking a detail-oriented Scheduler to join our team. The role involves completing detailed calculations to verify system design meets code and standard requirements, participating in pre/post project design meetings, and attending customer/site coordination meetings. The Scheduler will develop bills of materials to facilitate construction, support Project Managers to maintain or improve project margins, and manage the development, maintenance, and monitoring of construction CPM Schedules.<h2>Responsibilities</h2><ul><li>Verify system design meets code and standard requirements through detailed calculations.</li><li>Participate in pre/post project design meetings and attend customer/site coordination meetings.</li><li>Develop bills of materials to facilitate construction.</li><li>Provide support to Project Managers to maintain or improve project margins.</li><li>Develop, maintain, and monitor construction CPM Schedules.</li><li>Review project documents and specifications to develop baseline schedules including all required dates, activities, and milestones.</li><li>Perform progress schedule updates, including comprehensive reporting and narratives.</li><li>Manage resources and report accordingly.</li></ul><h2>Essential Skills</h2><ul><li>Experience with Primavera P6</li><li>Proficiency in Primavera, Bluebeam, Excel, Navisworks, and CAD</li><li>5+ years of experience in scheduling</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Associate or Bachelor's degree in construction management, mechanical, or drafting</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Green Bay, WI.Pay and BenefitsThe pay range for this position is $38.00 - $58.00/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 Green Bay,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.

Scheduler

Position Summary:Actalent 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 Project Controls Analyst/Scheduler will develop, maintain, and analyze project schedules using Primavera P6. They will provide cost loaded schedules as well as completed ready to execute resource loaded and logic driven schedules. They will conduct schedule maintenance, collect progress data, develop and implement project schedule/ status reports, and provide consistent, accurate information to the project team. They will mentor and train less experience Project Controls Analysts.Primary Duties and Responsibilities:<ul><li>Perform all Primavera project schedule and cost related updates throughout the lifecycle of projects assigned.</li><li>Interface with engineering, construction, planning, project management, and other transmission partners to verify updated Primavera schedule, resource, and cost information.</li><li>Conduct and lead project schedule baseline review meetings with team members.</li><li>Analyze project progress and make recommendations as to forecasted costs. </li><li>Maintain estimated costs in Primavera. </li><li>Perform final project assessment to ensure compliance with PCG standards. </li><li>Assist in developing metrics and measures for the TE&amp;PS project portfolio. </li><li>Participate in development of project control standards and guidelines. </li><li>Ensure planning, engineering, construction, and project management are following PLMP processes.</li><li>They will mentor and train less experience Project Controls Analysts.</li></ul>Education and Experience Requirements:<ul><li>Bachelor’s Degree in Construction Management, Engineering, Accounting, or Business</li><li>Three to seven years of experience in scheduling or project controls in construction</li><li>Three to seven years of experience interfacing with engineering, construction, planning, and project management</li><li>Three to seven years of experience using a scheduling software.</li></ul>Requisite Abilities and Skills:<ul><li>Demonstrate ability to manage time effectively and efficiently, show capable of having organizational and planning skills, as well as having an aptitude for accuracy and attention to detail.</li><li>Strong written and verbal communication </li><li>Team player with ability to work in a highly cross-functional and virtual environment</li><li>Ability to plan, set, and achieve goals </li><li>Superior level of personal character and integrity</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 $31.25 - $35.10/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 New Albany,OH.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: SchedulerJob DescriptionThe Scheduler position requires onsite presence in Muskogee, OK, working on a hyperscale data center project. The role involves assisting in the preparation, development, and updating of project schedules with the project team, including performing schedule reviews and communicating findings diplomatically. The Scheduler actively participates in construction planning and scheduling processes, supports Lean and Pull Planning sessions, and aids in the preparation of various reports for assigned projects.Responsibilities<ul><li>Assist in preparing, developing, and updating project schedules with the project team.</li><li>Perform schedule reviews to identify variations and notify project teams.</li><li>Diplomatically communicate review comments to the project team.</li><li>Participate in the creation of proposal schedules, baseline schedules, and ongoing schedule updates.</li><li>Utilize company-provided training of industry-standard scheduling software for proficiency.</li><li>Assist with the development of best practices for planning and scheduling efforts.</li><li>Review job status and apply ongoing changes to update project schedules.</li><li>Attend project-related meetings with an emphasis on schedule discussions.</li><li>Support Lean and Pull Planning sessions to ensure CPM schedule alignment.</li><li>Prepare reports required for assigned projects.</li><li>Add resource loading and cost loading to schedules as required.</li><li>Provide planning and scheduling support to operations, marketing, and other corporate functions.</li></ul>Essential Skills<ul><li>Experience with Primavera P6 software is preferred.</li><li>High school diploma or GED equivalent required.</li><li>Bachelor’s degree in Construction Management, Engineering, or Business Management, or at least three years of electrical field trade experience.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience in electrical mission critical hyperscale data center construction projects is highly preferred.</li><li>Knowledge of Installation Work Packages (IWP) in the hyperscale environment is highly preferred.</li></ul>Work EnvironmentThe work environment requires onsite presence in Muskogee, OK. Per diem is available for individuals whose homes are not in the general area, based on GSA rates, with travel home twice a month. The position is eligible for an annual bonus based on company performance and individual contribution. There is a bring-your-own-device policy, with a monthly reimbursement for business use of personal cell phones. The Scheduler will report to the Sr Project Manager and interface with the General Contractor/Owner and other contractors in a client-facing role.Job Type &amp; LocationThis is a Permanent position based out of Tulsa, OK.Pay and BenefitsThe pay range for this position is $110000.00 - $130000.00/yr.Workflex policy
Educational Assistance program after two years
Immediate PTO, birthday pay, and holiday pay
Volunteer community service paid time off
Parental and grandparent paid time off after one year
Bereavement paid time off
Company paid life insurance
Company paid disability insurance
Company paid Employee Assistance Program with counseling
Company paid financial education &amp; wellness program with budgeting resources
401K retirement plan with fully vested annual company contribution equal to 3% of compensation, and additional discretionary annual company contribution subject to vesting (not based on employee paycheck deferral contributions)
Health with HSA, Dental, and Vision insurance
Dependent Care FSA
Voluntary Life insurance
Voluntary Hospital Indemnity, Critical Illness, and Accident insurance plans
Voluntary Hinge Health Musculoskeletal Digital Exercise Therapy Program
Voluntary LegalShield and Identity Theft protection plans
Education 529 College Savings plan
Employee DiscountsWorkplace TypeThis is a fully onsite position in Tulsa,OK.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.

Overview:We are looking for an experienced Scheduler that will be responsible for building and maintaining an Integrated Master Schedule (IMS) and collaborating with the production team for inventory control and Manufacturing Order (MO) generation/closeout. This position will be supporting the Unmanned Systems Division.Description:<ul><li>Plans, prepares, issues and controls production schedules and coordinates with material requirements to ensure a controlled flow of approved materials timed to meet production requirements. </li><li>Advises management of the status of work in progress, material availability, and potential production problems to ensure that personnel, equipment, materials and services are provided as needed. </li><li>Schedules equipment and personnel, confirms material supply and demands, prepares work orders or purchase requests for the production or purchase of components or parts based on a master production schedule, shop load and inventory requirements. </li><li>Coordinates interdepartmental activity with quality assurance, manufacturing, purchasing, engineering, inventory control, traffic, etc.; schedules and expedites the movement of parts by means of move orders, stock transfers and requests for shipping orders.</li></ul>Qualifications:<ul><li>US Citizenship.</li><li>6 years relevant experience with Bachelors in related field preferred. High School Diploma or equivalent and 10 years relevant experience.</li><li>Mastery of MS Project required.</li><li>Proficiency with Primavera P6 desired.</li><li>Proficiency with MS Excel required.</li><li>Experience preparing, updating, and evaluating schedules and schedule metrics required.</li><li>Must be able to work independently and in team/group settings.</li><li>Must be able to obtain and maintain a government clearance. </li><li>Deltek/Costpoint (MRP) experience preferred but not required.</li></ul>Job Type &amp; LocationThis is a Permanent position based out of Virginia Beach, VA.Pay and BenefitsThe pay range for this position is $45.00 - $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 fully onsite position in Virginia Beach,VA.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 Controls Analyst / SchedulerJob Description:<ul><li>Perform all Primavera project schedule and cost related updates throughout the lifecycle of projects assigned.</li><li>Interface with engineering, construction, planning, project management, and other transmission partners to verify updated Primavera schedule, resource, and cost information.</li><li>Conduct and lead project schedule baseline review meetings with team members.</li><li>Analyze project progress and make recommendations as to forecasted costs.</li><li>Maintain estimated costs in Primavera.</li><li>Perform final project assessment to ensure compliance with PCG standards.</li><li>Assist in developing metrics and measures for the TE&amp;PS project portfolio.</li><li>Participate in development of project control standards and guidelines.</li><li>Ensure planning, engineering, construction, and project management are following PLMP processes.</li></ul>Job Type &amp; LocationThis is a Contract position based out of Tulsa, OK.Pay and BenefitsThe pay range for this position is $31.25 - $35.10/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 Tulsa,OK.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.

Project Controls Analyst / SchedulerJob Description:<ul><li>Perform all Primavera project schedule and cost related updates throughout the lifecycle of projects assigned.</li><li>Interface with engineering, construction, planning, project management, and other transmission partners to verify updated Primavera schedule, resource, and cost information.</li><li>Conduct and lead project schedule baseline review meetings with team members.</li><li>Analyze project progress and make recommendations as to forecasted costs.</li><li>Maintain estimated costs in Primavera.</li><li>Perform final project assessment to ensure compliance with PCG standards.</li><li>Assist in developing metrics and measures for the TE&amp;PS project portfolio.</li><li>Participate in development of project control standards and guidelines.</li><li>Ensure planning, engineering, construction, and project management are following PLMP processes.</li></ul>Job Type &amp; LocationThis is a Contract position based out of New Albany, OH.Pay and BenefitsThe pay range for this position is $31.25 - $35.10/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 New Albany,OH.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.

Job Title: SchedulerJob DescriptionAs a Scheduler, you will be responsible for developing and managing integrated project schedules using industry-standard tools. You will break down complex scopes into logical, resource-loaded activities and ensure regular updates based on contractor inputs and field progress.Responsibilities<ul><li>Build and maintain integrated project schedules using industry-standard tools, such as MS Project.</li><li>Break down complex project scopes into logical, resource-loaded activities with clear durations, predecessors, and constraints.</li><li>Update project schedules regularly based on contractor inputs, field progress, and internal milestones.</li><li>Perform critical path analysis, float analysis, and 'what if' scenario modeling to support project planning.</li><li>Generate weekly and monthly schedule reports for leadership, highlighting risks, variances, and recovery options.</li><li>Track procurement lead times, long lead items, and permitting timelines to ensure alignment with construction sequencing.</li></ul>Essential Skills<ul><li>3+ years of experience in construction scheduling, project controls, or related project management roles.</li><li>Proficiency with scheduling software, such as MS Project.</li><li>Strong understanding of construction sequencing, permitting processes, and trade coordination.</li><li>Ability to interpret construction drawings, specifications, and contractor schedules.</li><li>Excellent analytical skills with the ability to communicate complex information clearly.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience supporting large-scale commercial, industrial, or mission-critical construction projects.</li><li>Familiarity with construction delivery models or similar fast-paced, multi-project environments.</li><li>Experience with construction principles, Last Planner System, or pull planning.</li><li>Ability to influence without authority and drive alignment across diverse stakeholders.</li><li>Strong Excel and data analysis skills; comfort working with dashboards and reporting tools.</li></ul>Work EnvironmentThe work environment involves engaging with diverse stakeholders in a fast-paced setting. You'll work with advanced scheduling software and tools, and the role requires excellent communication skills to effectively convey complex information. The position may require coordinating with various departments to ensure project timelines and objectives are met.Job Type &amp; LocationThis is a Contract position based out of Seattle, WA.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 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.

<h2 style="text-align:center;">Actalent is Hiring a Team of Scientists // First and Second Shift!!</h2>Job DescriptionWe are seeking a dedicated Associate Scientist to perform routine tests on various samples including finished products, stability samples, raw materials, and more using techniques such as UV and HPLC in a regulated laboratory environment. The role involves evaluating test results, maintaining accurate lab documentation, and ensuring compliance with SOPs and cGMP standards.Responsibilities<ul><li>Conduct routine tests of finished products, stability samples, raw materials, and CV samples using techniques such as assays, chromatographic purity, and particle size distribution.</li><li>Evaluate test results and determine the acceptability of samples based on the results.</li><li>Maintain accurate lab notebooks and complete all related analytical reports and documentation in compliance with SOPs.</li><li>Ensure laboratories are maintained with good housekeeping practices and in compliance with cGMP standards.</li><li>Review notebooks promptly and ensure compliance with SOPs.</li><li>Analyze and interpret results in both written and oral formats.</li><li>Assist in training new analysts.</li><li>Conduct laboratory investigations and initiate Quality Events, CAPA, and Change Controls as needed.</li><li>Follow all SOPs and safety guidelines to ensure compliance with a cGMP environment.</li></ul>Essential Skills<ul><li>Proficiency in HPLC, UPLC, and UV-Vis techniques.</li><li>Strong analytical Familiarity with FDA and GMP regulations.</li><li>Ability to analyze and interpret complex data.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor’s degree in Chemistry or related scientific field with 1-2 years of related experience in pharmaceutical analysis, or a Master’s degree with 1 year of experience.</li><li>Problem-solving skills involving several concrete variables in standardized situations.</li><li>Ability to perform necessary computations and interpret graphs.</li><li>Working knowledge of instrumentation software used in laboratories.</li></ul>Work EnvironmentThis position is based in a lab environment regulated by FDA and GMP standards. Work schedule is 1st shift 8am-5pm OR 2nd shift 2pm-11pm, with all training taking place during the first shift. Job Type &amp; LocationThis is a Contract to Hire position based out of Coral Springs, FL.Pay and BenefitsThe pay range for this position is $29.00 - $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 Coral Springs,FL.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.

Scientist

<h2 style="text-align:center;">Actalent is Hiring a Team of Chemists // Second Shift!</h2>Job DescriptionWe are seeking dedicated Chemists to perform routine tests on various samples, including finished products, stability samples, raw materials, and more using techniques such as UV and HPLC in a regulated laboratory environment. The role involves evaluating test results, maintaining accurate lab documentation, and ensuring compliance with SOPs and cGMP standards.Responsibilities<ul><li>Conduct routine tests of finished products, stability samples, raw materials, and CV samples using techniques such as assays, chromatographic purity, and particle size distribution.</li><li>Evaluate test results and determine the acceptability of samples based on the results.</li><li>Maintain accurate lab notebooks and complete all related analytical reports and documentation in compliance with SOPs.</li><li>Ensure laboratories are maintained with good housekeeping practices and in compliance with cGMP standards.</li><li>Review notebooks promptly and ensure compliance with SOPs.</li><li>Analyze and interpret results in both written and oral formats.</li><li>Assist in training new analysts.</li><li>Conduct laboratory investigations and initiate Quality Events, CAPA, and Change Controls as needed.</li><li>Follow all SOPs and safety guidelines to ensure compliance with a cGMP environment.</li></ul>Essential Skills<ul><li>Proficiency in HPLC, UPLC, and UV-Vis techniques.</li><li>Strong analytical background in chemistry.</li><li>Familiarity with FDA and GMP regulations.</li><li>Ability to analyze and interpret complex data.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor’s degree in Chemistry or related scientific field with 1-2 years of related experience in pharmaceutical analysis, or a Master’s degree with 1 year of experience.</li><li>Problem-solving skills involving several concrete variables in standardized situations.</li><li>Ability to perform necessary computations and interpret graphs.</li><li>Working knowledge of instrumentation software used in laboratories.</li></ul>Work EnvironmentThis position is based in a lab environment regulated by FDA and GMP standards. Work schedule is 2nd shift 2pm-11pm, with all training taking place during the first shift.Job Type &amp; LocationThis is a Contract to Hire position based out of Boca Raton, FL.Pay and BenefitsThe pay range for this position is $29.00 - $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 Boca Raton,FL.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.

<h2 style="text-align:center;">Actalent is Hiring a Team of Chemists // First and Second Shift!!</h2>Job DescriptionWe are seeking a dedicated Associate Scientist to perform routine tests on various samples including finished products, stability samples, raw materials, and more using techniques such as UV and HPLC in a regulated laboratory environment. The role involves evaluating test results, maintaining accurate lab documentation, and ensuring compliance with SOPs and cGMP standards.Responsibilities<ul><li>Conduct routine tests of finished products, stability samples, raw materials, and CV samples using techniques such as assays, chromatographic purity, and particle size distribution.</li><li>Evaluate test results and determine the acceptability of samples based on the results.</li><li>Maintain accurate lab notebooks and complete all related analytical reports and documentation in compliance with SOPs.</li><li>Ensure laboratories are maintained with good housekeeping practices and in compliance with cGMP standards.</li><li>Review notebooks promptly and ensure compliance with SOPs.</li><li>Analyze and interpret results in both written and oral formats.</li><li>Assist in training new analysts.</li><li>Conduct laboratory investigations and initiate Quality Events, CAPA, and Change Controls as needed.</li><li>Follow all SOPs and safety guidelines to ensure compliance with a cGMP environment.</li></ul>Essential Skills<ul><li>Proficiency in HPLC, UPLC, and UV-Vis techniques.</li><li>Strong analytical background in chemistry.</li><li>Familiarity with FDA and GMP regulations.</li><li>Ability to analyze and interpret complex data.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor’s degree in Chemistry or related scientific field with 1-2 years of related experience in pharmaceutical analysis, or a Master’s degree with 1 year of experience.</li><li>Problem-solving skills involving several concrete variables in standardized situations.</li><li>Ability to perform necessary computations and interpret graphs.</li><li>Working knowledge of instrumentation software used in laboratories.</li></ul>Work EnvironmentThis position is based in a lab environment regulated by FDA and GMP standards. Work schedule is 1st shift 8am-5pm OR 2nd shift 2pm-11pm, with all training taking place during the first shift.Job Type &amp; LocationThis is a Contract to Hire position based out of Boca Raton, FL.Pay and BenefitsThe pay range for this position is $29.00 - $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 Boca Raton,FL.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.

Job Title: ScientistJob DescriptionThe Translational Pathology Biomarker Testing Laboratory (TPBTL) within the Translational Sciences organization is seeking a highly motivated, multidisciplinary scientist to assist with the development, implementation, and execution of biomarker testing for drug programs that have progressed to early phase clinical development. This position will primarily support immunohistochemistry (IHC) and in situ hybridization (ISH) assay development and clinical testing in a CLIA-certified, CAP-accredited laboratory. The role includes performing and documenting standardized experiments, assisting with specimen accessioning, testing, imaging, data analysis, quality control, report writing, and other tasks as needed. Additionally, responsibilities include general laboratory operational tasks such as maintaining laboratory equipment, ordering, and inventory management. The scientist will work in a dynamic, cross-functional team that includes pathologists, program managers, clinical technicians, data management, quality, regulatory, and management.Responsibilities<ul><li>Develop and validate immunohistochemistry (IHC) and in situ hybridization (ISH) assays.</li><li>Utilize microscopes and imaging systems, including commercial image analysis software packages, on a daily basis.</li><li>Independently plan and execute laboratory experiments, collect data, and communicate and present results to internal teams with guidance as needed.</li><li>Maintain current and broad knowledge in Molecular &amp; Cellular Biology, Cancer Biology, and Pathology.</li><li>Collect, analyze, and synthesize data into presentations, posters, and reports.</li><li>Assist in writing, following, and maintaining Standard Operating Procedures.</li><li>Work in a regulated environment associated with maintaining a high-performing CLIA-certified, CAP-accredited laboratory.</li><li>Order and maintain reagents and supplies, ensure instrument maintenance, and manage general lab operations.</li><li>Maintain a great team culture, participate in department initiatives, and seek career development opportunities.</li></ul>Essential Skills<ul><li>B.S. and 2+ years of laboratory experience; M.S. and 0-2 years in a biological science-related field.</li><li>Experience working in a laboratory setting.</li><li>Ability to follow and execute standard operating procedures.</li><li>Excellent written and oral communication skills.</li><li>Strong interpersonal skills and ability to work in a multi-disciplinary team environment.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience with molecular biology and/or histology techniques.</li><li>Experience working in a regulated clinical laboratory, CLIA and/or CAP environment is strongly preferred.</li><li>Knowledge in cancer biology, immunology, or histopathology.</li><li>Use of microscopes, imaging systems, and image analysis software.</li><li>Experience in multiplexing and/or fluorescent IHC, a plus.</li><li>Assay development using automated platforms.</li><li>Data management, data analysis, and statistical software packages.</li></ul>Work EnvironmentThe work environment involves working in a CLIA-certified, CAP-accredited laboratory. The position requires collaboration with a dynamic, cross-functional team including pathologists, program managers, clinical technicians, data management, quality, and regulatory professionals. The laboratory utilizes advanced microscopes, imaging systems, and commercial image analysis software packages. The role involves maintaining laboratory equipment and managing inventory in a regulated setting.Job Type &amp; LocationThis is a Contract position based out of Bothell, WA.Pay and BenefitsThe pay range for this position is $57.70 - $57.70/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 Bothell,WA.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.

<h2 style="text-align:center;">Actalent is Hiring a Team of Chemists // Second Shift!</h2>Job DescriptionWe are seeking dedicated Chemists to perform routine tests on various samples, including finished products, stability samples, raw materials, and more using techniques such as UV and HPLC in a regulated laboratory environment. The role involves evaluating test results, maintaining accurate lab documentation, and ensuring compliance with SOPs and cGMP standards.Responsibilities<ul><li>Conduct routine tests of finished products, stability samples, raw materials, and CV samples using techniques such as assays, chromatographic purity, and particle size distribution.</li><li>Evaluate test results and determine the acceptability of samples based on the results.</li><li>Maintain accurate lab notebooks and complete all related analytical reports and documentation in compliance with SOPs.</li><li>Ensure laboratories are maintained with good housekeeping practices and in compliance with cGMP standards.</li><li>Review notebooks promptly and ensure compliance with SOPs.</li><li>Analyze and interpret results in both written and oral formats.</li><li>Assist in training new analysts.</li><li>Conduct laboratory investigations and initiate Quality Events, CAPA, and Change Controls as needed.</li><li>Follow all SOPs and safety guidelines to ensure compliance with a cGMP environment.</li></ul>Essential Skills<ul><li>Proficiency in HPLC, UPLC, and UV-Vis techniques.</li><li>Strong analytical Experience in chemistry.</li><li>Familiarity with FDA and GMP regulations.</li><li>Ability to analyze and interpret complex data.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor’s degree in Chemistry or related scientific field with 1-2 years of related experience in pharmaceutical analysis, or a Master’s degree with 1 year of experience.</li><li>Problem-solving skills involving several concrete variables in standardized situations.</li><li>Ability to perform necessary computations and interpret graphs.</li><li>Working knowledge of instrumentation software used in laboratories.</li></ul>Work EnvironmentThis position is based in a lab environment regulated by FDA and GMP standards. Work schedule is 2nd shift 2pm-11pm, with all training taking place during the first shift.Contract to hire: 6 monthsPay Rate: $29- 35/hrJob Type &amp; LocationThis is a Contract to Hire position based out of Coral Springs, FL.Pay and BenefitsThe pay range for this position is $29.00 - $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 Coral Springs,FL.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.

<h2 style="text-align:center;">Associate Scientist/Chemist</h2>Job DescriptionWe are seeking dedicated Chemists to perform routine tests on various samples, including finished products, stability samples, raw materials, and more using techniques such as UV and HPLC in a regulated laboratory environment. The role involves evaluating test results, maintaining accurate lab documentation, and ensuring compliance with SOPs and cGMP standards.Responsibilities<ul><li>Conduct routine tests of finished products, stability samples, raw materials, and CV samples using techniques such as assays, chromatographic purity, and particle size distribution.</li><li>Evaluate test results and determine the acceptability of samples based on the results.</li><li>Maintain accurate lab notebooks and complete all related analytical reports and documentation in compliance with SOPs.</li><li>Ensure laboratories are maintained with good housekeeping practices and in compliance with cGMP standards.</li><li>Review notebooks promptly and ensure compliance with SOPs.</li><li>Analyze and interpret results in both written and oral formats.</li><li>Assist in training new analysts.</li><li>Conduct laboratory investigations and initiate Quality Events, CAPA, and Change Controls as needed.</li><li>Follow all SOPs and safety guidelines to ensure compliance with a cGMP environment.</li></ul>Essential Skills<ul><li>Proficiency in HPLC, UPLC, and UV-Vis techniques.</li><li>Strong analytical Experience in chemistry.</li><li>Familiarity with FDA and GMP regulations.</li><li>Ability to analyze and interpret complex data.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor’s degree in Chemistry or related scientific field with 1-2 years of related experience in pharmaceutical analysis, or a Master’s degree with 1 year of experience.</li><li>Problem-solving skills involving several concrete variables in standardized situations.</li><li>Ability to perform necessary computations and interpret graphs.</li><li>Working knowledge of instrumentation software used in laboratories.</li></ul>Work EnvironmentThis position is based in a lab environment regulated by FDA and GMP standards. Job Type &amp; LocationThis is a Contract to Hire position based out of Coral Springs, FL.Pay and BenefitsThe pay range for this position is $29.00 - $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 Coral Springs,FL.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.

We are seeking a collaborative, curious, and motivated contractor to join the Synthetic Molecule Pharmaceutics group, contributing to parenteral formulation development and drug‑delivery research for programs across our pipeline.Our team focuses on synthetic molecules and novel modalities—including nucleic acids, peptides, and conjugates—administered through parenteral routes such as intravenous, subcutaneous, intrathecal, and intravitreal delivery. We design formulations, advance innovative drug‑delivery strategies, and develop manufacturing processes that enable these novel therapeutics to reach patients across diverse disease areas.Responsibilities: <ul><li>Independently prepare drug‑product formulations of varying compositions to support pre‑clinical studies and pharmaceutics work packages</li><li>Develop and optimize drug‑product processes for both simple and complex dosage forms, including nanoparticle‑based formulations</li><li>Characterize formulations using a wide range of analytical techniques to assess physicochemical properties, composition, and structure</li><li>Clearly and promptly document experimental work in electronic lab notebooks and presentations</li><li>Analyze experimental data, identify trends and key insights, and propose hypothesis‑driven follow‑up studies</li><li>Collaborate with internal partners and external collaborators to deliver on project goals and share findings</li></ul>Job Type &amp; LocationThis is a Contract position based out of South San Francisco, CA.Pay and BenefitsThe pay range for this position is $40.00 - $48.00/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 South San Francisco,CA.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.

Scientist I

Scientist I (Molecular Biology)MUST have NGS experience (can be from academia but industry preferred) Job DescriptionThe Molecular Biologist will play a crucial role in the execution of verification and validation (V&amp;V) and research and development (R&amp;D) strategies designed by senior team members. The position is primarily laboratory-based, and candidates should have a strong background in molecular biological techniques, especially real-time PCR and NGS. A deep knowledge of the field and experience with quantitative PCR, digital drop PCR, or equivalent is essential. The role requires effective collaboration within a dynamic team, strong organizational skills, attention to detail, and the ability to maintain accurate records.Responsibilities<ul><li>Participate in training on new assays.</li><li>Conduct experiments related to clinical trials.</li><li>Share results and collaborate with other team members.</li></ul>Essential Skills<ul><li>Minimum of 3 years of direct laboratory testing experience in relevant specialties.</li><li>Strong experience in molecular biology techniques.</li><li>Hands-on experience with next-generation sequencing (NGS), preferably with Ion Torrent technology.</li><li>Proficiency in data analysis and the use of computer systems for data entry, retrieval, and analyses.</li></ul>Additional Skills &amp; Qualifications<ul><li>A BS degree in Biological Sciences is required; an MS degree in a molecular field is preferred.</li><li>Demonstrated ability to perform complex data analyses.</li><li>Excellent verbal and written communication skills.</li><li>Strong understanding of good laboratory practices and regulatory compliance.</li></ul>Work EnvironmentThis is an on-site position located in West Sacramento, California. The work is primarily laboratory-based, involving the handling of highly infectious agents and hazardous chemicals. The role requires the ability to sit or stand for long periods, handle equipment and specimens, and perform tasks that involve bending, stretching, and lifting up to 40 lbs. Visual acuity to distinguish colors and auditory ability to hear equipment timers are necessary. The position involves some office work, including writing experiments, validation documents, and standard operating procedures.Job Type &amp; LocationThis is a Contract to Hire position based out of West Sacramento, CA.Pay and BenefitsThe pay range for this position is $30.00 - $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 West Sacramento,CA.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.

Scientist I (Molecular Biology)

Scientist II (MUST HAVE NGS HANDS ON EXPERIENCE) Job DescriptionWe are seeking a dedicated Scientist II with substantial experience in molecular biology and PCR techniques to join our CAP-accredited CLIA laboratory in West Sacramento, California. This on-site position offers an opportunity to contribute to the development of new cancer tests and the application of new drugs for cancer patients enrolled in clinical trials. The ideal candidate will have a profound impact on the team and the advancement of cancer research.Responsibilities<ul><li>Train on new assays to stay updated with the latest methodologies.</li><li>Perform experiments related to clinical trials with precision and accuracy.</li><li>Share experimental results with team members to foster collaboration and innovation.</li></ul>Essential Skills<ul><li>At least 2-3 years of experience with PCR, Quantitative PCR, digital drop PCR, or equivalent techniques.</li><li>Minimum of 5 years of direct experience in laboratory testing for specialties performed by the Life Technologies Clinical Services Lab.</li><li>Hands-on experience with next-generation sequencing, preferably with Ion Torrent technology.</li><li>Proficiency in laboratory-based experimental techniques in a broad array of molecular biology methods.</li><li>Demonstrated ability to perform complex data analysis with strong analytical skills.</li></ul>Additional Skills &amp; Qualifications<ul><li>A BS degree in Biological Sciences from an accredited college or university is required.</li><li>An MS degree in a molecular field is preferred.</li><li>Excellent verbal and written communication skills.</li><li>Strong understanding of good laboratory practices and regulatory compliance.</li><li>Use of computer systems for data entry, retrieval, and analyses involving word processing programs, spreadsheets, and complex computer-driven instrumentation.</li><li>Ability to problem-solve highly complex analyses.</li></ul>Work EnvironmentThe role is primarily laboratory-based, requiring the handling of infectious agents and hazardous chemicals. Candidates must be able to sit or stand for extended periods, manipulate specimens, and operate equipment. Physical requirements include lifting up to 40 lbs, distinguishing colors for analysis, and auditory abilities to hear equipment timers. The work schedule is contingent, spanning Sunday to Saturday.Job Type &amp; LocationThis is a Contract to Hire position based out of West Sacramento, CA.Pay and BenefitsThe pay range for this position is $35.00 - $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 West Sacramento,CA.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.

Scientist II

Job Title: Scientist II (MUST HAVE NGS HANDS ON EXPERIENCE) Job DescriptionWe are seeking a dedicated Scientist II with substantial experience in molecular biology and PCR techniques to join our CAP-accredited CLIA laboratory in West Sacramento, California. This on-site position offers an opportunity to contribute to the development of new cancer tests and the application of new drugs for cancer patients enrolled in clinical trials. The ideal candidate will have a profound impact on the team and the advancement of cancer research.Responsibilities<ul><li>Train on new assays to stay updated with the latest methodologies.</li><li>Perform experiments related to clinical trials with precision and accuracy.</li><li>Share experimental results with team members to foster collaboration and innovation.</li></ul>Essential Skills<ul><li>At least 2-3 years of experience with PCR, Quantitative PCR, digital drop PCR, or equivalent techniques.</li><li>Minimum of 5 years of direct experience in laboratory testing for specialties performed by the Life Technologies Clinical Services Lab.</li><li>Hands-on experience with next-generation sequencing, preferably with Ion Torrent technology.</li><li>Proficiency in laboratory-based experimental techniques in a broad array of molecular biology methods.</li><li>Demonstrated ability to perform complex data analysis with strong analytical skills.</li></ul>Additional Skills &amp; Qualifications<ul><li>A BS degree in Biological Sciences from an accredited college or university is required.</li><li>An MS degree in a molecular field is preferred.</li><li>Excellent verbal and written communication skills.</li><li>Strong understanding of good laboratory practices and regulatory compliance.</li><li>Use of computer systems for data entry, retrieval, and analyses involving word processing programs, spreadsheets, and complex computer-driven instrumentation.</li><li>Ability to problem-solve highly complex analyses.</li></ul>Work EnvironmentThe role is primarily laboratory-based, requiring the handling of infectious agents and hazardous chemicals. Candidates must be able to sit or stand for extended periods, manipulate specimens, and operate equipment. Physical requirements include lifting up to 40 lbs, distinguishing colors for analysis, and auditory abilities to hear equipment timers. The work schedule is contingent, spanning Sunday to Saturday.Job Type &amp; LocationThis is a Contract position based out of West Sacramento, CA.Pay and BenefitsThe pay range for this position is $35.00 - $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 West Sacramento,CA.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: Scientist IIJob DescriptionWe are seeking a dedicated Scientist II to perform cGMP cell-based potency assays testing in support of the manufacture of biologics products. This role entails generating, compiling, and evaluating data for technical reports to support both commercial and clinical supplies. The successful candidate will be responsible for maintaining laboratory documentation, ensuring data integrity, and supporting regulatory inspections.Responsibilities<ul><li>Perform cGMP cell-based potency assays testing.</li><li>Generate, compile, and evaluate data for technical reports.</li><li>Review and approve raw data and laboratory logbooks/worksheets.</li><li>Perform cell culture and cell banking.</li><li>Manage critical reagents and supplies.</li><li>Write quality systems records including laboratory investigations, change controls, non-conformances.</li><li>Support regulatory inspections as needed.</li><li>Ensure proper use and maintenance of lab equipment, supporting equipment validation and preventive maintenance.</li><li>Generate and update standard operating procedures (SOPs).</li><li>Adhere to and support all Environmental Health and Safety (EHS) standards, procedures, and policies.</li><li>Understand regulations and business processes to maintain laboratory data integrity.</li></ul>Essential Skills<ul><li>Experience in a GMP regulated environment.</li><li>Experience in bioassays, Chemi-ECL ELISA, PCR and automation.</li><li>Experience with aseptic cell culture and cell banking.</li><li>Proficiency in quality systems.</li><li>Ability to perform laboratory investigations, change controls, and manage non-conformances.</li></ul>Additional Skills &amp; Qualifications<ul><li>MS in Chemistry/Biochemistry/Cell Biology or a related Biological Science field with 3+ years of relevant industrial experience.</li><li>BS in Chemistry/Biochemistry/Cell Biology or a related Biological Science field with 5+ years of relevant industrial experience.</li><li>Proficiency in Microsoft Project and Excel.</li></ul>Work EnvironmentThis is a 100% onsite role requiring full compliance with all governmental and legislative requirements. The position is a 1-year contract for one individual, offering an opportunity to work in a regulated environment committed to enhancing the welfare of customers, employees, and the community.Job Type &amp; LocationThis is a Contract position based out of Irvine, CA.Pay and BenefitsThe pay range for this position is $43.00 - $46.00/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 Irvine,CA.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: Scientist II - Antibody ConjugationJob DescriptionWe are seeking a dedicated Scientist II to join our Antibody Conjugation team on the 2nd shift in Carlsbad, CA. You will play a vital role in the production of fluorescent labeled bioconjugates, which are essential for cell signaling research initiatives.Responsibilities<ul><li>Perform conjugation of monoclonal and polyclonal antibodies.</li><li>Execute accurate and aseptic lab techniques, maintaining good documentation practices and adhering to good manufacturing practices.</li><li>Utilize general lab equipment such as centrifuges, spectrophotometers, and pipettes.</li><li>Conduct chromatography, buffer and reagent preparation, and use FPLC (AKTA) systems.</li><li>Initiate and manage Problem Reports for both planned and unplanned deviations and failures/nonconformities.</li><li>Act as an agent of change and provide leadership for peers.</li><li>Accurately document and complete all manufacturing batch records independently.</li><li>Create and revise documentation related to the department by opening change orders.</li><li>Navigate laboratory database systems efficiently.</li><li>Follow verbal and written instructions meticulously.</li><li>Ensure a clean and safe work environment is maintained.</li><li>Adhere to all departmental SOPs, guidelines, and procedures.</li><li>Address issues promptly and effectively.</li></ul>Essential Skills<ul><li>Bachelor's degree in chemistry or biological science.</li><li>2+ years of experience in cellular or microbiology laboratory techniques in a manufacturing or R&amp;D environment.</li><li>Proficiency with chromatography techniques.</li><li>Understanding of GLP and GMP processes and documentation.</li><li>Excellent communication skills and ability to work in a multidisciplinary team.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience with AKTA machines and bioconjugation is preferred.</li><li>Experience with fluorescently labeled antibodies.</li><li>Experience owning problem reports, deviations, or CAPAs.</li><li>Experience opening or revising change orders.</li><li>Familiarity with laboratory database systems/LIMS.</li><li>Background in biotech or life sciences manufacturing.</li><li>Demonstrated contributions to continuous improvement.</li><li>Informal leadership or peer mentoring experience.</li></ul>Work EnvironmentThis position is based in Carlsbad, CA, working a 40-hour week from Monday to Friday on the 2nd shift. The role involves regular sitting, standing, walking, talking, and hearing, as well as handling chemicals and lifting weights up to 20 pounds, with occasional assistance required for heavier items. The work environment requires adherence to safety practices to manage fumes, airborne particles, and toxic chemicals.Job Type &amp; LocationThis is a Contract position based out of Carlsbad, CA.Pay and BenefitsThe pay range for this position is $33.00 - $33.00/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 Carlsbad,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.

Job Title: Scientist II (MUST HAVE NGS HANDS ON EXPERIENCE) Job DescriptionWe are seeking a dedicated Scientist II with substantial experience in molecular biology and PCR techniques to join our CAP-accredited CLIA laboratory in West Sacramento, California. This on-site position offers an opportunity to contribute to the development of new cancer tests and the application of new drugs for cancer patients enrolled in clinical trials. The ideal candidate will have a profound impact on the team and the advancement of cancer research.Responsibilities<ul><li>Train on new assays to stay updated with the latest methodologies.</li><li>Perform experiments related to clinical trials with precision and accuracy.</li><li>Share experimental results with team members to foster collaboration and innovation.</li></ul>Essential Skills<ul><li>At least 2-3 years of experience with PCR, Quantitative PCR, digital drop PCR, or equivalent techniques.</li><li>Minimum of 5 years of direct experience in laboratory testing for specialties performed by the Life Technologies Clinical Services Lab.</li><li>Hands-on experience with next-generation sequencing, preferably with Ion Torrent technology.</li><li>Proficiency in laboratory-based experimental techniques in a broad array of molecular biology methods.</li><li>Demonstrated ability to perform complex data analysis with strong analytical skills.</li></ul>Additional Skills &amp; Qualifications<ul><li>A BS degree in Biological Sciences from an accredited college or university is required.</li><li>An MS degree in a molecular field is preferred.</li><li>Excellent verbal and written communication skills.</li><li>Strong understanding of good laboratory practices and regulatory compliance.</li><li>Use of computer systems for data entry, retrieval, and analyses involving word processing programs, spreadsheets, and complex computer-driven instrumentation.</li><li>Ability to problem-solve highly complex analyses.</li></ul>Work EnvironmentThe role is primarily laboratory-based, requiring the handling of infectious agents and hazardous chemicals. Candidates must be able to sit or stand for extended periods, manipulate specimens, and operate equipment. Physical requirements include lifting up to 40 lbs, distinguishing colors for analysis, and auditory abilities to hear equipment timers. The work schedule is contingent, spanning Sunday to Saturday.Job Type &amp; LocationThis is a Contract to Hire position based out of West Sacramento, CA.Pay and BenefitsThe pay range for this position is $35.00 - $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 West Sacramento,CA.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.

Job Title: Scientist IIIJob DescriptionThe Scientist III will be an integral part of the Quantitative, Translational &amp; ADME Sciences group, focusing on non-regulated quantitative LC MS/MS bioanalysis of small molecule compounds from various biological samples. This hands-on role involves working with mass spectrometry, specifically using AB Sciex triple quadrupole instrumentation and Analyst software. The scientist will execute methods, review data, and analyze samples, collaborating closely with discovery and DMPK teams.Responsibilities<ul><li>Perform high throughput quantitative LC MS/MS analysis of small molecules and occasionally peptides from various biological matrices.</li><li>Review and assess LC MS data to ensure data quality and integrity.</li><li>Execute established in vitro bioanalysis workflows with minor method development.</li><li>Operate, maintain, and troubleshoot AB Sciex triple quad LC MS/MS systems, HPLCs, and autosamplers.</li><li>Maintain accurate and compliant documentation in LIMS, method files, and study records.</li><li>Collaborate with cross-functional partners in Discovery and other departments to support project needs.</li><li>Design, execute, and interpret bioanalytical experiments independently.</li></ul>Essential Skills<ul><li>Extensive experience in quantitative LC MS/MS, especially with triple quadrupole systems.</li><li>Ability to work independently with minimal supervision.</li><li>Strong understanding of small molecule bioanalysis in biological matrices.</li><li>Proficiency with AB Sciex instruments and Analyst software.</li><li>Experience working with various biological matrices such as plasma, tissues, and microsomes.</li><li>Excellent data interpretation, documentation, and communication skills.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience with reverse phase chromatography method development is a plus.</li><li>Knowledge of peptide and protein bioanalysis is advantageous.</li><li>Familiarity with ADME principles, which can be learned on the job.</li><li>Experience in regulated bioanalysis or CRO environments is preferred.</li><li>Education requirements: BS with 8+ years, MS with 6+ years, or PhD with relevant experience in Biochemistry, Analytical Chemistry, or related fields.</li></ul>Work EnvironmentThe role is based 100% onsite at Abbott Park, working Monday through Friday from 8am to 5pm. It is a contract position for 6 months with potential extensions up to 2 years. The Scientist III will work independently within a collaborative team focused on mass spectrometry.Job Type &amp; LocationThis is a Contract position based out of North Chicago, IL.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 fully onsite position in North Chicago,IL.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.

Scientist III

<h2 style="text-align:center;">Associate Scientist/Chemist</h2>Job DescriptionWe are seeking dedicated Chemists to perform routine tests on various samples, including finished products, stability samples, raw materials, and more using techniques such as UV and HPLC in a regulated laboratory environment. The role involves evaluating test results, maintaining accurate lab documentation, and ensuring compliance with SOPs and cGMP standards.Responsibilities<ul><li>Conduct routine tests of finished products, stability samples, raw materials, and CV samples using techniques such as assays, chromatographic purity, and particle size distribution.</li><li>Evaluate test results and determine the acceptability of samples based on the results.</li><li>Maintain accurate lab notebooks and complete all related analytical reports and documentation in compliance with SOPs.</li><li>Ensure laboratories are maintained with good housekeeping practices and in compliance with cGMP standards.</li><li>Review notebooks promptly and ensure compliance with SOPs.</li><li>Analyze and interpret results in both written and oral formats.</li><li>Assist in training new analysts.</li><li>Conduct laboratory investigations and initiate Quality Events, CAPA, and Change Controls as needed.</li><li>Follow all SOPs and safety guidelines to ensure compliance with a cGMP environment.</li></ul>Essential Skills<ul><li>Proficiency in HPLC, UPLC, and UV-Vis techniques.</li><li>Strong analytical Experience in chemistry.</li><li>Familiarity with FDA and GMP regulations.</li><li>Ability to analyze and interpret complex data.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor’s degree in Chemistry or related scientific field with 1-2 years of related experience in pharmaceutical analysis, or a Master’s degree with 1 year of experience.</li><li>Problem-solving skills involving several concrete variables in standardized situations.</li><li>Ability to perform necessary computations and interpret graphs.</li><li>Working knowledge of instrumentation software used in laboratories.</li></ul>Work EnvironmentThis position is based in a lab environment regulated by FDA and GMP standards. Job Type &amp; LocationThis is a Contract to Hire position based out of Coconut Creek, FL.Pay and BenefitsThe pay range for this position is $29.00 - $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 Coconut Creek,FL.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.

Scientist/ QC/ Chermist

<h2 style="text-align:center;">Associate Scientist/Chemist</h2>Job DescriptionWe are seeking dedicated Chemists to perform routine tests on various samples, including finished products, stability samples, raw materials, and more using techniques such as UV and HPLC in a regulated laboratory environment. The role involves evaluating test results, maintaining accurate lab documentation, and ensuring compliance with SOPs and cGMP standards.Responsibilities<ul><li>Conduct routine tests of finished products, stability samples, raw materials, and CV samples using techniques such as assays, chromatographic purity, and particle size distribution.</li><li>Evaluate test results and determine the acceptability of samples based on the results.</li><li>Maintain accurate lab notebooks and complete all related analytical reports and documentation in compliance with SOPs.</li><li>Ensure laboratories are maintained with good housekeeping practices and in compliance with cGMP standards.</li><li>Review notebooks promptly and ensure compliance with SOPs.</li><li>Analyze and interpret results in both written and oral formats.</li><li>Assist in training new analysts.</li><li>Conduct laboratory investigations and initiate Quality Events, CAPA, and Change Controls as needed.</li><li>Follow all SOPs and safety guidelines to ensure compliance with a cGMP environment.</li></ul>Essential Skills<ul><li>Proficiency in HPLC, UPLC, and UV-Vis techniques.</li><li>Strong analytical Experience in chemistry.</li><li>Familiarity with FDA and GMP regulations.</li><li>Ability to analyze and interpret complex data.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor’s degree in Chemistry or related scientific field with 1-2 years of related experience in pharmaceutical analysis, or a Master’s degree with 1 year of experience.</li><li>Problem-solving skills involving several concrete variables in standardized situations.</li><li>Ability to perform necessary computations and interpret graphs.</li><li>Working knowledge of instrumentation software used in laboratories.</li></ul>Work EnvironmentThis position is based in a lab environment regulated by FDA and GMP standards. Job Type &amp; LocationThis is a Contract to Hire position based out of Fort Lauderdale, FL.Pay and BenefitsThe pay range for this position is $29.00 - $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 Fort Lauderdale,FL.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.

Scientist/chemist/ QC/Associate Scientist

<h2 style="text-align:center;">Scrum Master </h2>We are seeking a dedicated Scrum Master and Process Coordinator to manage scrums, enforce processes, and coordinate sprint planning for system design and development. This role involves overseeing coding, integration, and testing to ensure seamless project execution.Work schedule is 4, 10 hour days each week (Friday's Off). Will also be able to work remotely 2 days. Offer comes with Benefits, Paid Vacation and Paid Holidays. Responsibilities<ul><li>Manage and lead scrum meetings effectively.</li><li>Enforce processes to ensure adherence to agile methodologies.</li><li>Coordinate and manage sprint planning sessions.</li><li>Oversee system design, development, coding, integration, and testing processes.</li></ul>Essential Skills<ul><li>General knowledge of software design and development processes.</li><li>Experience with JIRA software for project management.</li><li>Proficiency in enforcing processes and conducting sprint planning.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor's degree in a related discipline or equivalent experience/combined education.</li><li>Experience with AGILE Development Process and backlog grooming.</li><li>Knowledge of C++ and Linux is desired.</li><li>Experience with implementing Agile ceremonies.</li></ul>Job Type &amp; LocationThis is a Contract position based out of Liverpool, NY.Pay and BenefitsThe pay range for this position is $45.00 - $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 Liverpool,NY.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.

Scrum Master (Hybrid Schedule)

We are looking for a highly skilled Software Development Engineer in Test (SDET) to be a member on our mobile engineering team. This role blends software development expertise with a strong focus on quality engineering and automated testing.•	Contributes to both functional and non-functional areas of testing.•	Functional testing includes testing from a functionality/requirements perspective and is largely driven by acceptance criteria or user stories. Key ResponsibilitiesTest Automation•	Design, develop, and maintain robust automated test frameworks for UI, API, and integration testing.•	Build scalable and reusable test automation solutions around the Flutter platform.•	Integrate automated testing into CI/CD YAML pipelines using the test automation platform built on Azure DevOps.•	Partner with test automation platform team on improvements to the test automation platform that serves many product teams.Quality Engineering &amp; Test Strategy•	Collaborate with developers, verification engineers, and product owners to define test strategies, acceptance criteria, and quality goals.•	Perform functional, regression, smoke, performance, and reliability testing.•	Implement shift-left testing practices, ensuring quality is embedded early in the SDLC.Engineering Collaboration &amp; Debugging•	Participate in design reviews &amp; code reviews to ensure testability and reliability.•	Partner closely with DevOps, test automation platform team and developers to improve release pipelines and automate reliability checks.•	Partner with the development team on building feature/functionality. Required: •	3 - 6+ years of progressive software development experience •	2+ years of hands-on mobile app development experience in Flutter and/or iOS (Swift) and/or Android (Kotlin), contributing to production codebases•	2+ years designing and implementing automated tests for mobile applications (unit + UI/widget + integration), including test maintenance and reliability improvements•	Strong understanding of mobile architecture, state management, and data flow, and ability to apply that understanding to improve testability and reliability•	Able to read, reason about, contribute to production code and provide code review feedback•	Ability to design meaningful, deterministic tests aligned to requirements and risk controls•	Skilled in unit, widget/UI, integration, and end to end test approaches•	Experience building reliable mobile automation (e.g., Flutter integration tests, simulators/mocks, and/or API automation)•	Experience integrating test execution into CI/CD and improves the pipeline signal (e.g., reducing flakiness, stabilizing environments/data)•	Ability to produce clear, complete verification evidence suitable for audits (objective evidence, clear steps, expected results)•	Experience with agile development methodologies and project management tools (e.g., JIRA, ADO, Agile/Scrum)Preferred: •	Experience with BrowserStack•	Experience with Cloud development in Azure•	Knowledge of healthcare industry standards and regulations (e.g., HIPAA compliance, IEC 62304)•	Experience with BLE interaction testing (pairing, reconnect, retries, error states) and diagnosing failure modes across mobile to embedded device to cloud boundaries•	Familiarity with structured verification workflows and tooling (e.g., test management, traceability systems)•	Medical device/SaMD background (regulated mobile preferred)Job Type &amp; LocationThis is a Contract position based out of Golden Valley, MN.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 hybrid position in Golden Valley,MN.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.

Sdet Software Developer In Test

Job Title: Senior Automation EngineerJob DescriptionWe are seeking a Senior Automation Engineer to design, develop, and implement automation control systems, including PLC, HMI, and SCADA solutions. This role involves programming and troubleshooting automation hardware and software, supporting the design and integration of robotics, motion control, and process automation systems, and collaborating with project teams to deliver custom automation solutions on time and within budget. The engineer will provide advanced technical support and mentorship to automation technicians and develop system documentation, ensuring compliance with applicable standards.Responsibilities<ul><li>Design, develop, and implement automation control systems, including PLC, HMI, and SCADA solutions.</li><li>Program and troubleshoot automation hardware and software, using platforms such as Allen-Bradley and Siemens.</li><li>Support the design and integration of robotics, motion control, and process automation systems.</li><li>Collaborate with project teams to deliver custom automation solutions on time and within budget.</li><li>Provide advanced technical support and mentorship to automation technicians.</li><li>Develop system documentation including control logic, schematics, and operation manuals.</li><li>Ensure compliance with applicable standards such as NFPA, NEC, UL 508A, and OSHA.</li><li>Participate in system commissioning, testing, and field service as required.</li><li>Develop bid strategies and review proposals for accuracy and competitiveness.</li><li>Maintain strong vendor and subcontractor relationships to support competitive pricing.</li><li>Provide oversight and technical guidance of UL508A panel shop operations.</li><li>Continually transform automation department processes and procedures.</li></ul>Essential Skills<ul><li>Bachelor’s degree in Electrical Engineering, Automation, Controls, or related field, or equivalent experience.</li><li>7+ years of experience in automation engineering, controls design, and programming.</li><li>Proficiency in PLC, HMI, and SCADA systems programming and troubleshooting (e.g., Rockwell/Allen-Bradley, Siemens).</li><li>Experience with RSLogix, FactoryTalk View, and Ignition.</li><li>Knowledge of industrial networks such as Ethernet/IP, Profibus, and Modbus.</li><li>Strong problem-solving skills and ability to work independently.</li><li>Excellent written and verbal communication skills.</li><li>Experience in commissioning and field startup.</li><li>Knowledge of relevant codes and standards (NFPA 70, NFPA 70B, UL 508A).</li><li>Industry experience in agricultural, food and beverage, and industrial markets.</li></ul>Additional Skills &amp; Qualifications<ul><li>Proficiency with automation &amp; controls software and estimating software.</li><li>Strong understanding of NEC, construction sequencing, and industry best practices.</li><li>Automation and controls experience with a focus on commercial and industrial construction.</li><li>Subject matter expertise in leading a team of technical professionals.</li><li>Experience with design-build or design-assist projects.</li><li>Familiarity with industrial and commercial electrical installations/projects.</li><li>Strong business acumen and ability to evaluate risk and profitability.</li><li>Knowledge of local labor markets, suppliers, and subcontractors.</li><li>Rockwell Automation badges.</li><li>Experience with industrial networking (EtherNet/IP, Modbus, DeviceNet, Profibus, etc.).</li><li>Template and standards creation (AutoCAD, PLC Programming, Ignition, etc.).</li><li>Familiarity with robotics and motion control.</li></ul>Work EnvironmentThe candidate will work in an office setting with the automation team, comprising a team of 5. This position involves approximately 25% travel, primarily across Kansas, with advanced notice for any overnight travel.Job Type &amp; LocationThis is a Contract to Hire position based out of Newton, KS.Pay and BenefitsThe pay range for this position is $62.50 - $76.92/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 Newton,KS.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.

Senior Automation Engineer

Lead Beverage Technologist - Newport NewsJob DescriptionWe are seeking a highly skilled Lead Beverage Technologist to drive the development of innovative, high‑quality finished food products that showcase new flavors and technologies. This role blends hands‑on formulation, trend‑driven concept creation, sensory analysis, and cross‑functional collaboration. The ideal candidate brings deep technical expertise, creativity, and leadership within the food development space.Responsibilities<ul><li>Create finished beverage products and transferable beverage technologies (alcoholic, non‑alcoholic, wine, spirits, canned cocktails, functional beverages, etc.).</li><li>Develop new beverage formulations, including specifications, processing instructions, and documentation for filling, mixing, carbonation, and scale‑up.</li><li>Lead beverage flavor innovation by producing prototypes, specifications, and finished product samples.</li><li>Identify and propose flavor, ingredient, and concept ideas for beverage market launches.</li><li>Collaborate with sales, marketing, beverage innovation teams, and foodservice to support customer projects and brand initiatives.</li><li>Direct and support beverage innovation teams for strategic launches and trend‑driven development.</li><li>Analyze and verify beverage sensory, technical, and lab data to guide formulation decisions.</li><li>Provide documentation for beverage launches, including specifications, prototypes, and sample submissions.</li><li>Support the transfer of beverage formulations for production across various technologies (RTD, spirits, sparkling, etc.).</li></ul>Essential Qualifications<ul><li>8–10+ years of experience in the food and beverage industry, with a strong focus on food development.</li><li>Bachelor’s Degree in Food Science, Chemistry, Biochemistry, or related field.</li><li>Strong skills in beverage manufacturing, laboratory testing, and product development.</li><li>Proficiency in Biology and Chemistry.</li><li>Experience developing function beverage systems</li></ul>Additional Skills<ul><li>Leadership experience in a food or beverage environment.</li><li>Expertise in flavor innovation and beverage ingredient performance.</li><li>Experience collaborating with sales, marketing, and technology teams.</li><li>Knowledge of regulations, beverage stability, and processing techniques.</li></ul>Work EnvironmentThe role is set in a lab environment where you will work in a small, intimate team, mixing flavors and developing products. Employees gain exposure to the entire lifecycle of a flavor, collaborating directly with customers to create the perfect product. This position offers a unique opportunity to work in a family-owned company.Job Type &amp; LocationThis is a Contract to Hire position based out of Newport News, VA.Pay and BenefitsThe pay range for this position is $28.80 - $48.07/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 Newport News,VA.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.

Senior Beverage Technologist

Job Title: ChemistJob DescriptionWe are seeking a Chemist to create, test, and refine new polymers and material formulations to drive product innovation. You will work closely with engineers, chemists, and designers to align materials, processes, and product requirements. Your contributions will be vital in the development and optimization of extrusion, lamination, thermoforming, and coating processes. You'll conduct bench-scale experiments and support pilot-scale trials to transition concepts toward production, while managing lab workflows and maintaining test methods.Responsibilities<ul><li>Develop and test new polymer and material formulations.</li><li>Collaborate with engineers, chemists, and designers to ensure material and process alignment.</li><li>Optimize extrusion, lamination, thermoforming, and coating processes.</li><li>Conduct bench-scale experiments and support pilot-scale trials.</li><li>Perform sample analysis and deliver insightful reports to guide next steps.</li><li>Manage lab workflows and oversee chemical inventory.</li><li>Organize daily lab priorities and testing schedules.</li><li>Assess laboratory equipment needs and support capital improvement initiatives.</li><li>Stay informed on emerging trends in polymer and materials science.</li><li>Provide occasional support for off-shift research activities or production trials.</li></ul>Essential Skills<ul><li>5+ years of experience in polymer science or chemical R&amp;D.</li><li>Hands-on lab experience with formulation, testing, and polymer synthesis.</li><li>Experience in scaling materials from lab to pilot plant.</li><li>Bachelor's degree in Chemistry, Polymer Science, or related field.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience in aerospace, flame/smoke/toxicity (FST), or regulated materials is a plus.</li></ul>Work EnvironmentThe position is based on a Monday to Friday schedule, with a flexible start time around 7:00 AM or 7:30 AM, as long as the required hours are fulfilled. The role involves 75% oversight and administrative tasks and 25% hands-on lab work. We offer a supportive work environment with health, dental, and vision benefits, 3-4 weeks of negotiable PTO, 11 paid holidays, and a 3% annual retirement contributionJob Type &amp; LocationThis is a Permanent position based out of Kent, OH.Pay and BenefitsThe pay range for this position is $120000.00 - $150000.00/yr.Health, dental and vision benefits 

PTO 3-4 weeks (negotiable) 

11 paid holidays 

3% annual retirement contributionWorkplace TypeThis is a fully onsite position in Kent,OH.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.

Senior Chemist

Job Title: Senior Civil/Structural EngineerJob DescriptionWe are seeking a detail-focused, knowledgeable, and professional Senior Structural Engineer to join our team. The ideal candidate will have a strong background in Structural or Civil Engineering with prior experience in large-scale projects. The key focus of this position is to design, build, and oversee building projects, ensuring cost efficiency and smooth running within budget and deadlines. This role involves interaction with government agencies, engineering firms, and construction companies. This is an excellent opportunity for someone to use their experience to impact one of the largest, most historic builds happening in the country in recent history. This site has 10 years of work planned, with multiple billions of dollars of investments allocated to these projects. This person can expect to gain competitive industry experience and have opportunity for growth.Responsibilities<ul><li>Oversee the planning and execution of projects, including budgets, schedules, and resources.</li><li>Design, develop, and review technical building and infrastructure plans and drawings.</li><li>Supervise the on-site team, ensuring the design and build concepts are being followed.</li><li>Ensure proper maintenance and servicing schedules are set out for the infrastructure.</li><li>Work with the project team to foresee and avoid obstacles during the construction or planning phases.</li><li>Adhere to health and safety guidelines at all times.</li><li>Provide project reports to executives.</li><li>Make suggestions for cost-reducing procedures for the projects.</li><li>Identify risk elements and determine how to mitigate them.</li><li>Coordinate with the Civil Engineer of Record (EOR) regarding government agencies and permitting/inspection requirements.</li></ul>Essential Skills<ul><li>B.S. or Master's degree in Structural Engineering, Civil Engineering, or a related field with a Professional Engineering (PE) certification.</li><li>3+ years of in-depth understanding and practical experience with international building regulations and construction sequence.</li><li>Strong analytical skills with keen attention to detail.</li><li>Ability to lead and supervise construction activities on-site performed by general contractors.</li></ul>Additional Skills &amp; Qualifications<ul><li>Knowledge of engineering principles, including land development, design, and construction.</li><li>Experience managing large construction projects in a similar role.</li><li>Experience with traffic engineering and flood control.</li><li>Excellent computer skills, including proficiency in AutoCAD and project management software.</li><li>Strong communication skills, both written and verbal.</li><li>Ability to work to agreed deadlines and timescales.</li><li>Demonstrated knowledge of health and safety guidelines.</li><li>Good problem-solving abilities.</li><li>Ability to prioritize time and workload efficiently.</li><li>Ability to collaborate effectively with cross-functional teams.</li></ul>Work EnvironmentWork Location: Phoenix, AZShift: Monday - FridayCandidates must be willing and able to work on-site at our Phoenix Arizona facility. We offer a comprehensive and competitive benefits program, including a variety of medical, dental, and vision plans, income-protection programs, a 401(k)-retirement savings plan, competitive paid time-off programs, and paid holidays.Job Type &amp; LocationThis is a Permanent position based out of Phoenix, AZ.Pay and BenefitsThe pay range for this position is $120000.00 - $147000.00/yr.Includes four major categories: Medical &amp; Insurance, Family Care, Wellness, Development &amp; Volunteering.
Each employee receives flexible benefit points equivalent to US$250 per year to spend based on their lifestyle needs.
Newly added benefit: Pet care, included for the first time.
High usage areas:

Family care (54%)
Medical &amp; InsuranceWorkplace TypeThis is a fully onsite position in Phoenix,AZ.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.

Senior Civil/structural Engineer

Job Title: Senior Clinical Database ProgrammerJob DescriptionDesign, program, and validate clinical trial reports, listings, and visualizations using tools such as SAS, R, or Python. Collaborate with stakeholders to understand the scope of work, requirements, plan, and execute deliverables in collaboration with data managers, clinical programmers, and management while adhering to established protocols.Responsibilities Design, program, and validate clinical trial reports, listings, and visualizations using tools such as SAS, R, or Python.· Collaborate with stakeholders to understand the scope of work, requirements, plan, and execute deliverables in collaboration with data managers, clinical programmers, and management while adhering to established timelines.· Demonstrated experience in programming, testing and validating programs and reports after development, ensuring accuracy, reliability, and compliance with regulatory and organizational standards.· Strong ability to document specifications, validation processes and results, maintaining comprehensive records.· Proven ability to support clinical review processes through the development, validation, and maintenance of robust, reliable, and innovative programming solutions.· Experience with quality assurance processes and methodologies within clinical data management, including knowledge of Good Clinical Practice (GCP) and other relevant regulatory guidelines.· A deep understanding of the importance of data integrity in clinical trials, with the ability to design and implement processes that ensure the consistency, accuracy, and reliability of clinical data throughout the trial lifecycle.· Experience with automation tools and techniques to improve the efficiency of clinical programming tasks, including the testing and validation phases. Familiarity with scripting and automation in R, Python, or SAS is a plus.· Serve as a technical resource for the programming group, providing guidance on complex programming tasks, standards, and processes.· In-depth knowledge of industry regulations and standards, including 21 CFR Part 11, CDISC (Clinical Data Interchange Standards Consortium), and ICH guidelines, with the ability to ensure all programming activities are compliant.· Experience with version control systems and change management processes, ensuring that all changes to programming code and datasets are tracked, documented, and controlled.· Excellent communication skills, with the ability to clearly document programming activities, testing results, and validation processes, and effectively communicate findings and recommendations to both technical and non-technical stakeholders.<ul><li>· Participate in project management cross-functional teams that work on standard operating procedures, guidelines, process improvements, system validation and acquisition, customization and integration of new tools and technologies.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor’s in computer science or health-related field and/or related discipline with 6-8 years of experience in clinical programming or relevant work experience.</li><li>Experience in CRO or CDM vendor management in oncology.</li><li>Early phase adaptive trial management experience preferred.</li><li>Experience with CDASH terminology.</li><li>Experience with R or SAS programming techniques is a plus.</li><li>Experience with Rave, Spotfire, and/or JReview is a plus.</li><li>Self-motivated and takes pride in your work.</li><li>Results-oriented team player who enjoys working collaboratively and building positive relationships.</li><li>Attention to detail and ability to proactively identify issues with a solutions-oriented approach.</li></ul>Work EnvironmentThis is a fully remote position operating on West Coast hours.Job Type &amp; LocationThis is a Contract position based out of South San Francisco, CA.Pay and BenefitsThe pay range for this position is $80.00 - $110.00/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 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.

Senior Clinical Database Programmer

Job Title: Senior Clinical Trial ManagerJob DescriptionWe are seeking a Senior Clinical Trial Manager to oversee and manage all clinical site interactions, including IRB/EC applications, contract negotiations, enrollment tracking, and issue resolution. This role involves owning and managing trial start-up, conduct, and close-out activities according to industry and corporate standards, contributing to key clinical documents, and establishing professional rapport with investigational site personnel.Responsibilities<ul><li>Manage all clinical site interactions including IRB/EC applications, contract negotiations, enrollment tracking, clinical trial material and clinical supply requests, and issue resolution.</li><li>Own and manage all trial start-up, conduct, and close-out activities according to industry and corporate standards.</li><li>Contribute to preparation of key clinical documents such as protocols, informed consent, amendments, CRFs, training materials, project plans, monitoring plans, data plans, SAPs, and reports.</li><li>Establish professional rapport and frequent communication with investigational site personnel.</li><li>Track internal metrics, timelines, and budgets.</li><li>Communicate trial status and prepare/present updates to management.</li><li>Oversee monitoring activities to ensure compliance with GCP, ICH, FDA regulations, SOPs, and protocols.</li><li>Interact with data management teams to plan and execute analyses.</li><li>Support applications and technical files as needed.</li><li>Collaborate with DSMB, CEC, and other committees.</li><li>Assist with investigators’ meetings and manage vendors.</li><li>Travel up to 25% of the time.</li><li>Perform other duties as assigned.</li></ul>Essential Skills<ul><li>8-10 years of clinical research experience with at least 3-5 years of trial management experience.</li><li>Medical device experience required.</li><li>Previous monitoring experience highly preferred.</li><li>Expertise in IRB/EC submissions and approvals.</li><li>Track record leading complex global clinical trials.</li></ul>Additional Skills &amp; Qualifications<ul><li>Cardiovascular experience preferred.</li></ul>Work EnvironmentThe position is based in Andover, MA, and will initially require full on-site work for the first three months. Following this period, the role will transition to a hybrid schedule, working four days a week on-site. The clinical operations team is a small, collaborative group of 13 people, embodying a 'lean and mean' ethos.Job Type &amp; LocationThis is a Contract to Hire position based out of Andover, MA.Pay and BenefitsThe pay range for this position is $70.00 - $80.00/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 Andover,MA.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.

Senior Clinical Trial Manager

Learn more about free job search tools, learning opportunities, and exclusive member events.

Discover CareerCircle

Access resources to advance your job search and career growth.

Tools & Training

Explore a wide range of job opportunities that match your skills and career goals.

Search Jobs

Create a professional resume that captures the attention of top employers with our easy-to-use tool.

Resume Builder

Prepare for your next interview with our expert tips and strategies.

Interview Prep

Discover in-depth profiles of leading employers to find your ideal workplace.

Search Companies

Develop in-demand skills with curated courses for today’s job market.

Courses

Access career resources and job postings anytime, anywhere with our app.

Mobile App

Source skilled talent and build your team.

Talent Acquisition

Access skilled talent ready to excel via our AI-driven platform, virtual events, and recruitment services.

CareerCircle TalentConnect

Transform your workforce and hiring practices with essential training and continuing education.

InclusiveU

Broaden your talent pool with dedicated support for individuals with disabilities.

Getting Hired Powered by CareerCircle

Mission aligned solutions supporting Non-Profit Organizations, Educational Institutions, Local Workforce Development Boards, and Learning Providers.

Upskilling & Job Advocacy

Upskilling solutions designed to empower members with in-demand skills training and ongoing support for successful certificate completion.

CareerReady

Job advocacy solutions to connect job seekers to inclusive employers through dedicated recruiting support.

CareerAdvocacy

Learn how we connect all communities with careers and build skilled talent pipelines.

About CareerCircle

Discover answers to common questions and gain insights into our goals and services.

Reach out to us for inquiries, support, or to learn more about our mission and services.

Contact

Explore our blog for latest news and trends for job seekers and employers.

Blog

Access our virtual career fairs, job seeker workshops, and employer focused webinars.

Events

Discover valuable resources to enhance your hiring strategy and drive organizational success.

Employer Resources

Get the latest news and updates on our mission, partnerships, and community impact.

Actalent Jobs

Browse Actalent Jobs

JOB SEEKERS

EMPLOYERS

COMMUNITY PARTNERS

ABOUT

RESOURCES