Job Title: R&amp;D TechnicianJob DescriptionThe Research Technician II in Cell Production is responsible for performing routine and innovative laboratory tasks, including cell plating, expansion, media changes, and sampling to complete various R&amp;D experiments. The role requires maintaining laboratory records, equipment, and inventory as per the written procedures, and assisting senior staff with evolving experimental needs. This position thrives in a collaborative team environment, contributing valuable input to enhance cell culture processes within the R&amp;D department.Responsibilities<ul><li>Perform large-scale primary cell culture in 2D to support research and process development activities for a tissue-engineered product with minimal direct supervision.</li><li>Assist with the generation and upkeep of all master and working cell banks to ensure optimal functionality and longevity.</li><li>Collect, prepare, and submit analytical samples with accuracy and timeliness.</li><li>Perform routine disinfection of the cleanroom and laboratory.</li><li>Monitor inventory of supplies and equipment used in the laboratory to ensure availability and timely replenishment.</li><li>Generate and provide data for technical reports.</li><li>Adhere to good aseptic techniques as outlined in SOPs.</li><li>Ensure adherence to all defined practices and communicate any non-conformance to the supervisor and appropriate team members.</li><li>Assist with drafting protocols, procedures, SOPs, and master batch records.</li><li>Follow protocols/procedures/SOPs and demonstrate some ability to resolve issues and process deviations.</li><li>Identify issues or problems and alert team lead or supervisor.</li></ul>Essential Skills<ul><li>Bioreactor operation</li><li>Research &amp; development</li><li>Cell culture</li><li>Aseptic technique</li><li>2-3 years of extensive mammalian cell culture experience (large upscale)</li><li>2-3 years of laboratory experience</li><li>GMP Experience</li></ul>Additional Skills &amp; Qualifications<ul><li>Ability to maintain a sterile work environment and lab setting</li><li>Experience drafting protocols and SOPs</li><li>Experience with technical report generation</li></ul>Work EnvironmentThe work environment is characterized by a 'work hard, play hard' ethos, providing opportunities to engage with leadership and learn about the company. The role is part of a smaller team within the R&amp;D side of the business, fostering a collaborative and dynamic setting. The company is dedicated to improving lives through biotechnology innovations.Job Type &amp; LocationThis is a Contract position based out of Eden Prairie, MN.Pay and BenefitsThe pay range for this position is $20.00 - $23.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Eden Prairie,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.

public

R&D Technician

R&amp;D TechnicianJob DescriptionThe Research Technician II in Cell Production is responsible for performing routine and innovative laboratory tasks, including cell plating, expansion, media changes, and sampling to complete various R&amp;D experiments. The role requires maintaining laboratory records, equipment, and inventory as per the written procedures, and assisting staff with evolving experimental needs. This position thrives in a collaborative team environment, contributing valuable input to enhance cell culture processes within the R&amp;D department.Responsibilities<ul><li>Perform large-scale primary cell culture in 2D to support research and process development activities for a tissue-engineered product with minimal direct supervision.</li><li>Assist with the generation and upkeep of all master and working cell banks to ensure optimal functionality and longevity.</li><li>Collect, prepare, and submit analytical samples with accuracy and timeliness.</li><li>Perform routine disinfection of the cleanroom and laboratory.</li><li>Monitor inventory of supplies and equipment used in the laboratory to ensure availability and timely replenishment.</li><li>Generate and provide data for technical reports.</li><li>Adhere to good aseptic techniques as outlined in SOPs.</li><li>Ensure adherence to all defined practices and communicate any non-conformance to the supervisor and appropriate team members.</li><li>Assist with drafting protocols, procedures, SOPs, and master batch records.</li><li>Follow protocols/procedures/SOPs and demonstrate some ability to resolve issues and process deviations.</li><li>Identify issues or problems and alert team lead or supervisor.</li></ul>Essential Skills<ul><li>Bioreactor operation</li><li>Research &amp; development</li><li>Cell culture</li><li>Aseptic technique</li><li>2-3 years of extensive mammalian cell culture experience (large upscale)</li><li>2-3 years of laboratory experience</li><li>GMP Experience</li></ul>Job Type &amp; LocationThis is a Contract position based out of Eden Prairie, MN.Pay and BenefitsThe pay range for this position is $20.00 - $23.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Eden Prairie,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.

EU MDR Specialist - R&amp;D EngineerJob DescriptionWe are seeking an experienced R&amp;D Engineer with deep expertise in the EU Medical Device Regulation (EU MDR 2017/745) to join our team. This role will support the design, development, documentation, and compliance strategy for medical devices intended for the EU market. The ideal candidate has a strong engineering foundation combined with hands-on experience navigating EU MDR requirements throughout the product lifecycle. As part of the R&amp;D organization, you will collaborate closely with Regulatory Affairs, Quality Assurance, Clinical, and Manufacturing to ensure that products meet both technical performance expectations and global regulatory obligations.Responsibilities<ul><li>Lead and support remediation design activities for medical devices in accordance with EU MDR.</li><li>Conduct engineering studies, testing, and technical evaluations, ensuring design controls are fully aligned with regulatory requirements.</li><li>Generate technical documentation including design inputs/outputs, risk analyses, verification and validation protocols, and test reports.</li><li>Develop, update, and maintain Technical Documentation (TD) and Technical Files to satisfy EU MDR Annex II and III requirements.</li><li>Ensure compliance with General Safety and Performance Requirements (GSPR).</li><li>Support clinical evaluation, post-market surveillance, and post-market clinical follow-up documentation as needed.</li><li>Perform and maintain risk management activities, supporting FMEA, fault-tree analysis, and other risk assessment tools.</li><li>Work with Quality to ensure design documentation, DHFs, and updates meet internal SOPs and external regulatory standards.</li><li>Support manufacturing transfer activities and design changes.</li><li>Contribute to project planning, schedule development, and technical decision making.</li><li>Design and execute verification and validation (V&amp;V) testing to demonstrate safety, performance, and regulatory compliance.</li><li>Lead investigations of design issues, CAPAs, and nonconformances impacting EU markets.</li></ul>Essential Skills<ul><li>Bachelor’s or Master’s degree in Mechanical, Biomedical, Electrical, or related Engineering field.</li><li>3–7+ years of experience in R&amp;D within the medical device industry.</li><li>Demonstrated experience preparing EU MDR–compliant technical documentation.</li><li>Thorough understanding of design controls (21 CFR 820.30) and ISO/IEC standards related to the product type.</li><li>Proven experience interacting with Notified Bodies or supporting NB audits.</li><li>Excellent technical writing skills and ability to produce audit-ready documentation.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience with Class IIb or Class III medical devices.</li><li>Prior experience with EU MDD-to-MDR transition projects.</li><li>Experience with coordinating with Regulatory Affairs to address Notified Body questions, audits, and remediation actions.</li><li>SolidWorks and Windchill experience.</li><li>Experience following IEC medical electrical equipment safety requirements.</li></ul>Work EnvironmentThis position is 100% onsite based in Denver, Colorado. The role requires occasional lab work, device testing, and hands-on engineering activities. There may be occasional travel, less than 10%, for training or team meetings. The company offers 2 weeks of PTO and 6 paid holidays.Job Type &amp; LocationThis is a Contract position based out of Centennial, CO.Pay and BenefitsThe pay range for this position is $55.00 - $57.69/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 Centennial,CO.Application DeadlineThis position is anticipated to close on Feb 20, 2026.<h2>About Actalent</h2>

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

R&d Engineer

Job Title: Research and Development EngineerJob DescriptionThe Research and Development Engineer leads research, design, and development of components and complex assemblies for critical bioprocessing applications. This individual supports innovation and product development through all stages, from ideation and concept, to prototyping, and through commercialization. The role involves working with the R&amp;D team on new product introduction (NPI), supporting production and process engineering, creating manufacturing packages, and assisting with quality/customer complaints.Responsibilities<ul><li>Translate business needs and market trends into product requirements and innovative engineering solutions.</li><li>Stay current with emerging technologies, materials, and industry trends to maintain competitive advantage.</li><li>Drive innovation by exploring new technologies, tools, and methodologies.</li><li>Support intellectual property strategies by identifying patentable technologies and collaborating with the legal team.</li><li>Partner with cross-functional teams to ensure successful product development and launch, adhering to established stage-gated process and governance model.</li><li>Effectively manage project timelines, budgets, and resources to deliver high-quality results.</li><li>Oversee the planning, design, development, prototyping, testing, and validation of new products and technologies.</li><li>Conduct risk assessments using the FMEA framework and drive risk mitigations as required. Lead design and drawing reviews as needed.</li><li>Ensure compliance with applicable regulatory, safety, and quality standards throughout the development process.</li><li>Lead problem-solving, corrective, and preventative actions around product concerns originating both external and internal to the organization.</li><li>Analyze data from validation tests to determine whether systems and processes meet required criteria and specifications.</li><li>Maintain technical records within design history files.</li><li>Drive continuous improvement in product performance, design for manufacturability (DFM), and design for cost-effectiveness. Implement engineering best practices, design standards, and documentation protocols. Author SOPs, Work Instructions, and Templates.</li><li>Support Product Delivery Teams (PDT), including creating and reviewing quality documents, participating in Corrective And Preventive Action (CAPA) implementation, and generating or supporting ECR (Engineering Change Request) &amp; ECO (Engineering Change Order) activities.</li><li>Collaborate with scientists and engineers internally and externally to assess and develop appropriate design and manufacturing specifications.</li><li>Perform other duties as assigned.</li></ul>Essential Skills<ul><li>7+ years of engineering experience within a biotechnology or pharmaceutical manufacturing facility.</li><li>4+ years of Single-Use Technology (SUT) design experience, preferably with tubing, bags, and filling needles.</li><li>Expertise in the design of molded plastic parts and assemblies for fluid handling of leak-proof applications.</li><li>Thorough understanding of industry standards and regulatory guidelines, such as ISO.</li><li>Track record in product development, from concept through commercialization.</li><li>Ability to manage multiple projects in a fast-paced, collaborative environment.</li><li>Results-driven mindset with keen sense of urgency and ability to deliver ahead of deadlines.</li><li>Demonstrated attention to detail with excellent follow-up skills.</li><li>Self-motivated, adaptable to various work projects, and efficient working independently and as part of a team.</li><li>Strong knowledge of design controls, prototyping technologies such as 3D printing, testing, and validation methodologies.</li><li>Ability to read, comprehend, and interpret documents such as drawings, BOMs, blueprints, and operating procedures.</li><li>Ability to train and guide less experienced personnel on proper interpretation and best practices.</li><li>Maintain organized and controlled records of all drawings and BOMs.</li><li>Drive and facilitate assigned portions of product change management and control.</li><li>Solid understanding of mathematical fundamentals including plane and solid geometry, fractions, percentages, ratios, and proportions applied to practical situations.</li><li>Ability to interpret complex data sets, identify patterns, and draw meaningful conclusions.</li><li>Author scientific reports with conclusions and recommendations.</li><li>Use data to drive decisions tied to the business context.</li><li>Expert knowledge and demonstrated hands-on experience with CAD software, both 3D and 2D.</li><li>Proficient with Microsoft Office Suite or related software.</li></ul>Additional Skills &amp; Qualifications<ul><li>Exposure to both medical device and biopharma industries.</li><li>Opportunities for patent authorship.</li><li>Direct customer interaction.</li><li>Autonomy in design and testing.</li></ul>Work EnvironmentThe work environment offers a collaborative atmosphere where innovation is encouraged. Engineers have autonomy in design and testing, and there is exposure to both medical device and biopharma industries. The role involves direct customer interaction and provides opportunities for patent authorship. The environment is fast-paced, requiring efficient project management and adherence to regulatory standards. Dress code is professionalJob Type &amp; LocationThis is a Permanent position based out of Camarillo, CA.Pay and BenefitsThe pay range for this position is $110000.00 - $130000.00/yr.Internal company benefits providedWorkplace TypeThis is a fully onsite position in Camarillo,CA.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: Research and Development EngineerJob DescriptionThe Research and Development Engineer leads research, design, and development of components and complex assemblies for critical bioprocessing applications. This individual supports innovation and product development through all stages, from ideation and concept, to prototyping, and through commercialization. The role involves working with the R&amp;D team on new product introduction (NPI), supporting production and process engineering, creating manufacturing packages, and assisting with quality/customer complaints.Responsibilities<ul><li>Translate business needs and market trends into product requirements and innovative engineering solutions.</li><li>Stay current with emerging technologies, materials, and industry trends to maintain competitive advantage.</li><li>Drive innovation by exploring new technologies, tools, and methodologies.</li><li>Support intellectual property strategies by identifying patentable technologies and collaborating with the legal team.</li><li>Partner with cross-functional teams to ensure successful product development and launch, adhering to established stage-gated process and governance model.</li><li>Effectively manage project timelines, budgets, and resources to deliver high-quality results.</li><li>Oversee the planning, design, development, prototyping, testing, and validation of new products and technologies.</li><li>Conduct risk assessments using the FMEA framework and drive risk mitigations as required. Lead design and drawing reviews as needed.</li><li>Ensure compliance with applicable regulatory, safety, and quality standards throughout the development process.</li><li>Lead problem-solving, corrective, and preventative actions around product concerns originating both external and internal to the organization.</li><li>Analyze data from validation tests to determine whether systems and processes meet required criteria and specifications.</li><li>Maintain technical records within design history files.</li><li>Drive continuous improvement in product performance, design for manufacturability (DFM), and design for cost-effectiveness. Implement engineering best practices, design standards, and documentation protocols. Author SOPs, Work Instructions, and Templates.</li><li>Support Product Delivery Teams (PDT), including creating and reviewing quality documents, participating in Corrective And Preventive Action (CAPA) implementation, and generating or supporting ECR (Engineering Change Request) &amp; ECO (Engineering Change Order) activities.</li><li>Collaborate with scientists and engineers internally and externally to assess and develop appropriate design and manufacturing specifications.</li><li>Perform other duties as assigned.</li></ul>Essential Skills<ul><li>7+ years of engineering experience within a biotechnology or pharmaceutical manufacturing facility.</li><li>4+ years of Single-Use Technology (SUT) design experience, preferably with tubing, bags, and filling needles.</li><li>Expertise in the design of molded plastic parts and assemblies for fluid handling of leak-proof applications.</li><li>Thorough understanding of industry standards and regulatory guidelines, such as ISO.</li><li>Track record in product development, from concept through commercialization.</li><li>Ability to manage multiple projects in a fast-paced, collaborative environment.</li><li>Results-driven mindset with keen sense of urgency and ability to deliver ahead of deadlines.</li><li>Demonstrated attention to detail with excellent follow-up skills.</li><li>Self-motivated, adaptable to various work projects, and efficient working independently and as part of a team.</li><li>Strong knowledge of design controls, prototyping technologies such as 3D printing, testing, and validation methodologies.</li><li>Ability to read, comprehend, and interpret documents such as drawings, BOMs, blueprints, and operating procedures.</li><li>Ability to train and guide less experienced personnel on proper interpretation and best practices.</li><li>Maintain organized and controlled records of all drawings and BOMs.</li><li>Drive and facilitate assigned portions of product change management and control.</li><li>Solid understanding of mathematical fundamentals including plane and solid geometry, fractions, percentages, ratios, and proportions applied to practical situations.</li><li>Ability to interpret complex data sets, identify patterns, and draw meaningful conclusions.</li><li>Author scientific reports with conclusions and recommendations.</li><li>Use data to drive decisions tied to the business context.</li><li>Expert knowledge and demonstrated hands-on experience with CAD software, both 3D and 2D.</li><li>Proficient with Microsoft Office Suite or related software.</li></ul>Additional Skills &amp; Qualifications<ul><li>Exposure to both medical device and biopharma industries.</li><li>Opportunities for patent authorship.</li><li>Direct customer interaction.</li><li>Autonomy in design and testing.</li></ul>Work EnvironmentThe work environment offers a collaborative atmosphere where innovation is encouraged. Engineers have autonomy in design and testing, and there is exposure to both medical device and biopharma industries. The role involves direct customer interaction and provides opportunities for patent authorship. The environment is fast-paced, requiring efficient project management and adherence to regulatory standards. Dress code is professionalJob Type &amp; LocationThis is a Permanent position based out of Camarillo, CA.Pay and BenefitsThe pay range for this position is $110000.00 - $130000.00/yr.Internal company benefits providedWorkplace TypeThis is a fully onsite position in Camarillo,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: R&amp;D Engineering TechnicianJob DescriptionJoin our innovative team as an R&amp;D Engineering Technician, where you will be at the forefront of creating the next generation of connectivity solutions. You will work in a dynamic environment alongside a diverse group of talented individuals, contributing to groundbreaking projects that challenge and inspire. This role involves conducting lab tests and documenting findings to support our engineering initiatives.Responsibilities<ul><li>Conduct lab tests and experiments, accounting for 75% of your role.</li><li>Document and report test results and findings, contributing 25% of your responsibilities.</li><li>Collaborate with engineers and other team members to ensure accurate and reliable test outcomes.</li><li>Utilize advanced mechanical and electronic test equipment effectively.</li></ul>Essential Skills<ul><li>Associate's degree, preferably in electronics.</li><li>1-3 years of experience in a related role.</li><li>Advanced skills in using mechanical and electronics test equipment in a lab setting.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience in fiberoptic cable installation or quality backgrounds is beneficial.</li><li>Strong verbal and written communication skills.</li><li>Ability to learn quickly and adapt to new challenges.</li></ul>Work EnvironmentThis position is onsite and operates during the 2nd shift from 1:30pm to 9:30pm. You will work alongside 7 testing engineering technicians, fostering a collaborative and supportive environment. The company is committed to maintaining a diverse and inclusive workplace, providing equal employment opportunities without regard to race, gender, disability, or protected veteran status.Job Type &amp; LocationThis is a Contract position based out of Richmond, IN.Pay and BenefitsThe pay range for this position is $40000.00 - $45000.00/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 Richmond,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.

R&d Engineering Technician

Experience Level<ul><li>Entry LevelExternal Communities Job DescriptionThis position contains the responsibility to Define, Implement, and Perform Electronic, Optical, Physical and Mechanical Laboratory Measurement, Evaluation, Analysis, Process and Procedures for Fiber Optic and Cable Products to provide technical assistance for the marketing manufacture, testing, sale and application of Belden's products.</li><li>Conduct a variety of electronic, optical, mechanical and/or physical tests on developmental or production units or components for the purpose of providing engineering groups with information and data which can be used in the analysis of product design, product performance, materials or manufacturing methods.</li><li>Assist in design of test methods or equipment for the purpose of conducting tests according to established industrial, governmental or customer requirements. Recommend changes to existing procedures to provide more accurate results or increased information for use by engineers. Audit and write new laboratory procedures.</li><li>Maintain test logs, records and prepare test reports to complete test program. Analyzed and discuss test findings with cognizant lab or engineering personnel to aid in data interpretation.</li><li>Interprets data, reports conclusions and makes recommendations for improvements based on observations of performance and testing to aid engineers in project completion.</li></ul>Required Skills and Experience<ul><li>Associate's Degree preferable in Electronics or related field or equivalent experience.</li><li>Advanced skillsets in the use of mechanical, electronic and optical test equipment within a laboratory environment.</li><li>1-3 years of experience in a related role.</li><li>MS Office experience.</li><li>Technical software experience a plus.</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Richmond, IN.Pay and BenefitsThe pay range for this position is $40000.00 - $45000.00/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 Richmond,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.

R&amp;D Engineering - NPI Testing and TroubleshootingJob DescriptionJoin our team as an R&amp;D Engineer, where you will support the New Product Introduction (NPI) testing, inspecting, and troubleshooting of balloon catheters. This role is ideal for candidates with experience in balloon catheter development, although those with extensive catheter experience are encouraged to apply.Responsibilities<ul><li>Conduct NPI testing, inspection, and troubleshooting of balloon catheters.</li><li>Utilize microscopes and handheld equipment for detailed inspection tasks.</li><li>Perform testing using Instron/tensile testing, balloon compliance testing, and fatigue testing.</li><li>Follow cleanroom protocols and maintain high standards of cleanliness and precision.</li><li>Collaborate within a team environment to support the development of innovative catheter products.</li></ul>Essential Skills<ul><li>Experience with catheter testing, inspections, and troubleshooting.</li><li>Proficiency in using microscopes and small hand tools.</li><li>Understanding of cleanroom practices and protocols.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience in prototyping and balloon compliance testing.</li><li>Familiarity with electromechanical design of catheter products.</li><li>Open to candidates with experience in NPI development, even without full-cycle exposure.</li></ul>Work EnvironmentThe role is based in Santa Clara, working at a state-of-the-art facility. It is a Monday through Friday, on-site position with flexible start times between 7am and 9am, totaling an 8-hour shift. The position offers a 9-month contract with the potential for conversion based on performance and approval.Job Type &amp; LocationThis is a Contract position based out of Santa Clara, CA.Pay and BenefitsThe pay range for this position is $39.00 - $39.00/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 Santa Clara,CA.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: R&amp;D Engineering TechnicianJob DescriptionJoin our innovative team as an R&amp;D Engineering Technician, where you will be at the forefront of creating the next generation of connectivity solutions. You will work in a dynamic environment alongside a diverse group of talented individuals, contributing to groundbreaking projects that challenge and inspire. This role involves conducting lab tests and documenting findings to support our engineering initiatives.Responsibilities<ul><li>Conduct lab tests and experiments, accounting for 75% of your role.</li><li>Document and report test results and findings, contributing 25% of your responsibilities.</li><li>Collaborate with engineers and other team members to ensure accurate and reliable test outcomes.</li><li>Utilize advanced mechanical and electronic test equipment effectively.</li></ul>Essential Skills<ul><li>Associate's degree, preferably in electronics.</li><li>1-3 years of experience in a related role.</li><li>Advanced skills in using mechanical and electronics test equipment in a lab setting.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience in fiberoptic cable installation or quality backgrounds is beneficial.</li><li>Strong verbal and written communication skills.</li><li>Ability to learn quickly and adapt to new challenges.</li></ul>Work EnvironmentThis position is onsite and operates during the 2nd shift from 1:30pm to 9:30pm. You will work alongside 7 testing engineering technicians, fostering a collaborative and supportive environment. The company is committed to maintaining a diverse and inclusive workplace, providing equal employment opportunities without regard to race, gender, disability, or protected veteran status.Job Type &amp; LocationThis is a Contract position based out of Richmond, IN.Pay and BenefitsThe pay range for this position is $40000.00 - $45000.00/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 Richmond,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: R&amp;D Formulation Scientist - CapsulesJob DescriptionWe are seeking a passionate R&amp;D Formulation Scientist to partner closely with sales and customers, addressing product requirements and technical needs. This role involves developing innovative formulations for oils, waters, soft gels, two-piece capsules, powders, and granulations. You will collaborate with sourcing and purchasing teams to ensure material availability and cost efficiency, and troubleshoot technical formulation issues, offering expert problem-solving support. The position also includes assisting with analytical testing and quality assessments, performing hands-on work in the product development laboratory, and utilizing analytical instrumentation such as GC, HPLC, and ICP-MS. You will evaluate laboratory capabilities and identify opportunities for future R&amp;D expansion, while working effectively within a predominantly Spanish-speaking laboratory team.Responsibilities<ul><li>Partner closely with sales and customers to support product requirements and technical needs.</li><li>Develop formulations for various products including oils, waters, soft gels, two-piece capsules, powders, and granulations.</li><li>Collaborate with sourcing and purchasing teams to ensure material availability and cost efficiency.</li><li>Troubleshoot technical formulation issues and provide expert problem-solving support.</li><li>Assist with analytical testing and quality assessments.</li><li>Perform hands-on work in the product development laboratory.</li><li>Utilize analytical instrumentation such as GC, HPLC, and ICP-MS.</li><li>Evaluate laboratory capabilities and identify opportunities for future R&amp;D expansion.</li><li>Work effectively with a predominantly Spanish-speaking laboratory team.</li></ul>Essential Skills<ul><li>Bachelor's Degree in Food Science, Chemistry, or a related field.</li><li>3+ years of R&amp;D formulation experience.</li><li>Expertise in powder, liquid, and capsule formulations.</li><li>Required nutraceutical experience with manufacturing knowledge.</li><li>Skilled in HPLC, GC, and ICP.</li><li>Analytical chemistry expertise.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bilingual skills are a plus.</li><li>Experience with raw material and quality control.</li><li>Knowledge in fish oils.</li></ul>Work EnvironmentThe role reports to the Quality Director until a future R&amp;D Director is hired. Currently, there are only two R&amp;D formulators on the team, which will expand following an acquisition. The shift is Monday to Friday, 8 AM to 5 PM, with 100% on-site work. The dress code is business casual.Job Type &amp; LocationThis is a Permanent position based out of Clifton, NJ.Pay and BenefitsThe pay range for this position is $75000.00 - $90000.00/yr.401K, holiday, vacation and sick time offered to internal employees. Will have potential to grow into a leadership role - the R&amp;D department is new and there will be room to expand to R&amp;D formulators that report to them.Workplace TypeThis is a fully onsite position in Clifton,NJ.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.

R&d Formulation Scientist - Capsules

Job Title: R&amp;D Formulation Scientist - Soft GelJob DescriptionJoin our dynamic team as an R&amp;D Formulation Scientist specializing in Soft Gel products. You will play a pivotal role in supporting product requirements and technical needs by partnering closely with Sales and Customers. This position involves developing innovative formulations for oils, waters, soft gels, two-piece capsules, powders, and granulations.Responsibilities<ul><li>Collaborate with Sourcing and Purchasing teams to ensure material availability and cost efficiency.</li><li>Troubleshoot technical formulation issues and provide expert problem-solving support.</li><li>Assist with analytical testing and quality assessments.</li><li>Perform hands-on work in the Product Development laboratory.</li><li>Utilize analytical instrumentation including GC, HPLC, and ICP-MS.</li><li>Evaluate laboratory capabilities and identify opportunities for future R&amp;D expansion.</li><li>Work effectively with a predominantly Spanish-speaking laboratory team; bilingual skills are not required, but comfort using translation tools is helpful.</li></ul>Essential Skills<ul><li>Bachelor's Degree in Food Science, Chemistry or related field.</li><li>3+ years of R&amp;D formulation experience.</li><li>Expertise in Soft Gels.</li><li>Required nutraceutical experience with manufacturing knowledge.</li><li>Skilled in HPLC, GC, and ICP.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bilingual skills are a plus.</li><li>Experience with raw material quality control.</li><li>Analytical chemistry expertise.</li><li>Knowledge of fish oils.</li></ul>Work EnvironmentYou will report to the Quality Director until a future R&amp;D Director is hired. Currently, there are only two R&amp;D formulators on the team, but the team will expand following the acquisition. The position involves working Monday to Friday, from 8 AM to 5 PM, 100% on-site. The dress code is business casual.Job Type &amp; LocationThis is a Permanent position based out of Clifton, NJ.Pay and BenefitsThe pay range for this position is $75000.00 - $90000.00/yr.401K, holidays and vacation hours along with sick time. Will be able to have a team under them in the future for the new R&amp;D department!Workplace TypeThis is a fully onsite position in Clifton,NJ.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.

R&d Formulation Scientist - Soft Gel

Job Title: R&amp;D Formulation Scientist - Soft GelJob DescriptionJoin our dynamic team as an R&amp;D Formulation Scientist specializing in Soft Gel products. You will play a pivotal role in supporting product requirements and technical needs by partnering closely with Sales and Customers. This position involves developing innovative formulations for oils, waters, soft gels, two-piece capsules, powders, and granulations.Responsibilities<ul><li>Collaborate with Sourcing and Purchasing teams to ensure material availability and cost efficiency.</li><li>Troubleshoot technical formulation issues and provide expert problem-solving support.</li><li>Assist with analytical testing and quality assessments.</li><li>Perform hands-on work in the Product Development laboratory.</li><li>Utilize analytical instrumentation including GC, HPLC, and ICP-MS.</li><li>Evaluate laboratory capabilities and identify opportunities for future R&amp;D expansion.</li><li>Work effectively with a predominantly Spanish-speaking laboratory team; bilingual skills are not required, but comfort using translation tools is helpful.</li></ul>Essential Skills<ul><li>Bachelor's Degree in Food Science, Chemistry or related field.</li><li>3+ years of R&amp;D formulation experience.</li><li>Expertise in Soft Gels.</li><li>Required nutraceutical experience with manufacturing knowledge.</li><li>Skilled in HPLC, GC, and ICP.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bilingual skills are a plus.</li><li>Experience with raw material quality control.</li><li>Analytical chemistry expertise.</li><li>Knowledge of fish oils.</li></ul>Work EnvironmentYou will report to the Quality Director until a future R&amp;D Director is hired. Currently, there are only two R&amp;D formulators on the team, but the team will expand following the acquisition. The position involves working Monday to Friday, from 8 AM to 5 PM, 100% on-site. The dress code is business casual.Job Type &amp; LocationThis is a Permanent position based out of Clifton, NJ.Pay and BenefitsThe pay range for this position is $75000.00 - $90000.00/yr.401K, holidays and vacation hours along with sick time. Will be able to have a team under them in the future for the new R&amp;D department!Workplace TypeThis is a fully onsite position in Clifton,NJ.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.

REMOTE Clinical Trial ManagerSmall BiotechMust support west coast hoursreports to the Sr. CTMJob DescriptionSupport the Study Lead and Study Execution Team (SET) to ensure trials are initiated efficiently and completed on time, within budget, and in compliance with Standard Operating Procedures (SOPs), FDA regulations, and ICH/GCP guidelines with minimal supervision. Collaborate with SET to develop, review, and facilitate Request for Proposals (RFPs), and contribute to bid defense meetings to select Contract Research Organizations (CROs) and other clinical vendors for the right strategic fit.Responsibilities<ul><li>Manage various clinical vendors to ensure that project and corporate goals are achieved on time and within budget, including review of monitoring reports, recruitment, and quality metrics in collaboration with CRO.</li><li>Actively manage and resolve site issues in collaboration with other functional lines and the CRO partner.</li><li>Contribute to the development and review of key clinical documents such as protocols, informed consent forms (ICFs), case report forms (CRFs), study reference manuals, and study plans.</li><li>Serve as a subject matter expert (SME) on various company/department initiatives and participate in the development, review, and implementation of departmental SOPs and processes.</li><li>Oversee and manage vendor contracts, forecast financials in partnership with finance, reconcile invoices against accruals, and ensure the accuracy of all CRO/vendor work order and change order updates.</li><li>Participate in the implementation and oversight of clinical systems including CTMS, TMF, EDC, and IRT.</li><li>Conduct clinical data review of data listings and summary tables, including query generation.</li><li>Engage in other study activities as needed, such as site selection, start-up, recruitment, protocol deviation, and TMF review.</li><li>Provide input and support in the development and review of key study documents, including protocols, ICFs, CRFs, study plans, Clinical Study Reports (CSR), and track key study metrics and progress reports.</li><li>Anticipate complex obstacles and clinical trial challenges, and implement creative solutions to achieve project goals and timelines.</li><li>Proactively identify potential study risks, recommend mitigation strategies/solutions, and facilitate discussions with internal and external stakeholders for implementation.</li><li>Establish and maintain strong relationships with internal cross-functional teams, CROs and vendors, and clinical research site personnel for successful execution of clinical trials.</li><li>Train investigators and site staff, vendors, and team members on study protocol and trial conduct processes.</li><li>Ensure that the Trial Master File (TMF) is set up and maintained appropriately throughout the trial, and conduct periodic TMF reviews/QCs as needed.</li><li>Ensure the clinical trial(s) are inspection-ready at all times and participate in Quality Assurance and/or regulatory authority inspection audits as needed.</li></ul>Essential Skills<ul><li>Clinical trial management experience, particularly in oncology and early phase trials.</li><li>Must be at CTM level with global study and vendor management experience.</li><li>Bachelor's degree in life sciences or related discipline with 6+ years of experience in clinical and drug development.</li><li>Advanced knowledge of domestic and global clinical study management and vendor management experience in oncology.</li><li>Understanding and implementation of FDA and ICH/GCP regulations and guidelines.</li><li>Self-motivated with a drive for continuous improvement and innovative thinking.</li><li>Results-oriented team player who enjoys collaboration and building positive relationships.</li><li>Detail-oriented and creative thinker with a passion for process optimization.</li><li>Excellent organizational, analytical, and communication (verbal and written) skills.</li><li>Ability to analyze and triage problems, prioritize accordingly, and propose solutions.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience in early phase oncology trial management, including precision medicine trials.</li></ul>Work EnvironmentThis position offers a remote work environment, providing flexibility and a dynamic, fast-paced atmosphere in a rapidly growing company.Job Type &amp; LocationThis is a Contract position based out of Houston, TX.Pay and BenefitsThe pay range for this position is $80.00 - $107.00/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 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.

REMOTE Clinical Trial Manager

Job Title: Flight Test Engineer - REMOTEJob DescriptionWe are seeking a skilled and experienced Flight Test Engineer to join our team. The role involves developing and executing flight test plans, analyzing test data, and collaborating with cross-functional teams to ensure the success of our aviation projects.Responsibilities<ul><li>Support the development of flight test plans, test cards, and test objectives aligned with program and system requirements.</li><li>Define test configurations, instrumentation needs, and data collection strategies.</li><li>Coordinate with systems, controls, and operations teams to ensure test readiness.</li><li>Participate in aircraft ground and flight test activities, supporting pre-flight, in-flight, and post-flight operations.</li><li>Monitor aircraft systems and telemetry during test execution to identify anomalies or safety concerns.</li><li>Support real-time decision-making during test events in collaboration with pilots, flight test leads, and engineering teams.</li><li>Analyze flight test data to assess system performance, aircraft behavior, and compliance with test objectives.</li><li>Correlate flight test results with system expectations, simulations, or analytical models.</li><li>Document findings, anomalies, and lessons learned, and communicate results to cross-functional teams.</li><li>Work closely with systems, controls, avionics, and simulation engineers to investigate issues and support root-cause analysis.</li><li>Support refinement of test procedures and system designs based on flight test outcomes.</li><li>Contribute to continuous improvement of flight test processes and documentation.</li></ul>Essential Skills<ul><li>Minimum of 3 years of experience working as a Flight Test Engineer.</li><li>At least 3 years of hands-on experience with aircraft flight test execution, including ground and/or flight activities.</li><li>Experience developing or supporting flight test plans and test procedures.</li><li>Strong experience in flight test data analysis and post-flight reporting.</li><li>Systems-level understanding of aircraft and subsystem interactions.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience supporting autonomous, optionally piloted, or experimental aircraft programs.</li><li>Familiarity with telemetry systems, data acquisition, or flight test instrumentation.</li><li>Experience working alongside flight controls or simulation teams.</li><li>Exposure to simulation-based test planning or test correlation.</li><li>Experience in regulated aerospace environments or certification-adjacent testing.</li></ul>Work EnvironmentThis position offers a fully remote work environment, allowing you the flexibility to manage your work-life balance while contributing to cutting-edge aviation projects.Job Type &amp; LocationThis is a Contract position based out of Houston, TX.Pay and BenefitsThe pay range for this position is $55.00 - $66.00/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 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.

REMOTE Flight Test Engineer

Job Title: Simulation EngineerJob DescriptionWe are seeking a Simulation Engineer to develop, maintain, and validate simulation models for aircraft aerodynamics, flight dynamics, and control systems. This role involves building MATLAB/Simulink models, implementing simulation logic using C++, and collaborating with engineering teams to ensure accurate and regulatory-aligned simulations.Responsibilities<ul><li>Develop, maintain, and validate simulation models for aircraft aerodynamics, flight dynamics, and control systems.</li><li>Build and refine MATLAB/Simulink models to support model-based design, analysis, and testing.</li><li>Implement simulation logic and performance models using C++ for integration with broader simulation frameworks.</li><li>Support simulation-based evaluation of aircraft behavior across nominal and off-nominal conditions.</li><li>Collaborate with systems, controls, and flight test engineers to correlate simulation results with real-world flight data.</li><li>Contribute to certification-oriented simulation efforts, including environments aligned with FAA Part 60 where applicable.</li><li>Support verification, validation, and documentation of simulation models to ensure accuracy and regulatory alignment.</li></ul>Essential Skills<ul><li>Understanding of aircraft aerodynamics, flight dynamics, and control systems.</li><li>Hands-on experience developing models using MATLAB/Simulink.</li><li>Professional experience with C++.</li><li>Experience working with or supporting flight test data, including model correlation or validation.</li><li>Experience working collaboratively across simulation, systems, and controls engineering teams.</li></ul>Additional Skills &amp; Qualifications<ul><li>Master's or PhD in engineering or related field.</li><li>Experience with FAA Part 60 simulation environments or certification-related simulation efforts.</li><li>Experience supporting autonomous, optionally piloted, or advanced aircraft systems.</li><li>Familiarity with verification and validation of simulation models in regulated aerospace environments.</li><li>Experience integrating Simulink models into larger software or simulation frameworks.</li><li>Exposure to hardware-in-the-loop (HIL), software-in-the-loop (SIL), or model-in-the-loop (MIL) environments.</li></ul>Work EnvironmentThis position offers a fully remote work environment, allowing flexibility and convenience while engaging in cutting-edge simulation projects.Job Type &amp; LocationThis is a Contract position based out of Phoenix, AZ.Pay and BenefitsThe pay range for this position is $55.00 - $66.00/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 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.

REMOTE Simulation Engineer - Matlab, C++

Job Title: Displays Focal EngineerJob DescriptionThis role involves being the primary engineer for aircraft display systems, ensuring that system requirements are comprehensively defined, verified, and aligned with aircraft architecture and operational needs.Responsibilities<ul><li>Act as the focal engineer for aircraft display systems, supporting system-level requirements definition and decomposition.</li><li>Ensure display system requirements align with overall aircraft system architecture and operational needs.</li><li>Support requirements validation, verification, and certification activities in compliance with ARP4754A.</li><li>Author, review, and manage system and subsystem requirements using Jama.</li><li>Maintain bidirectional traceability between requirements, design artifacts, and verification evidence.</li><li>Support audits and certification reviews by ensuring requirements completeness and traceability.</li><li>Develop, review, and execute system-level and subsystem-level test procedures.</li><li>Apply appropriate requirement verification methods, including analysis, test, inspection, and demonstration.</li><li>Ensure verification activities and artifacts comply with ARP4754A verification and traceability processes.</li><li>Investigate and reproduce issues originating from flight crew observations and flight test activities.</li><li>Perform system- and subsystem-level troubleshooting and fault isolation.</li><li>Correlate flight test data with system requirements and expected system behavior.</li><li>Manage problem reports, verification tasks, and workflows using Jira.</li><li>Configure and maintain Jira dashboards, filters, and reports to support engineering project tracking and visibility.</li><li>Support cross-functional teams by clearly communicating issue status, impacts, and resolution progress.</li></ul>Essential Skills<ul><li>Minimum of 3 years of displays engineering experience on commercial aircrafts.</li><li>Experience in ARP4745A system development lifecycle.</li><li>Proficiency with Jama for requirements management.</li><li>Experience with Jira for configuration and issue management.</li></ul>Additional Skills &amp; Qualifications<ul><li>5 years of commercial aircraft displays engineering experience is preferred.</li><li>Familiarity with Simulink.</li><li>Master's or PhD in engineering or a similar degree is highly advantageous.</li></ul>Work EnvironmentThe position is fully remote, offering flexibility and the opportunity to work from the comfort of your home.Job Type &amp; LocationThis is a Contract position based out of Houston, TX.Pay and BenefitsThe pay range for this position is $55.00 - $66.00/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 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.

REMOTE: Displays Focal Engineer

Job Title: RF Technician AJob DescriptionWe are seeking a skilled technician to repair remote radio heads and baseband units. The ideal candidate will have a solid understanding of RF signals and 4G/5G technologies, as well as expertise in electronics components and troubleshooting. PCB soldering experience is essential, and IPC certification is a plus. Proficiency with a multimeter is required, while experience with oscilloscopes and spectrum analyzers is preferred. Experience with Ericsson repairs is highly valued.Responsibilities<ul><li>Use soldering equipment to repair, modify, and replace parts on electronic circuit boards for remote radio heads and baseband units.</li><li>Validate symptoms and diagnose issues using information from automated diagnostic machines.</li><li>Disassemble devices, identify defective components, and perform PCB repairs.</li><li>Reassemble and test units to ensure they are fully functional.</li><li>Troubleshoot electronic components to the component level, resolving complex technical issues.</li><li>Read and interpret schematics.</li><li>Maintain satisfactory quality performance levels.</li><li>Keep a clean and organized workstation.</li><li>Train and assist other technicians in repair processes.</li></ul>Essential Skills<ul><li>Electronics certification.</li><li>Minimum of 2 years' experience as a Repair Technician or equivalent.</li><li>Proficient in soldering and desoldering techniques.</li><li>In-depth knowledge of electronic circuit components and theory.</li><li>Basic understanding of RF signals and 4G/5G technologies.</li><li>Proficiency with multimeters.</li><li>Experience with PCB repair.</li><li>Ability to read and interpret schematics.</li></ul>Additional Skills &amp; Qualifications<ul><li>IPC certification.</li><li>Experience with oscilloscopes and spectrum analyzers.</li><li>Previous experience with Ericsson repairs.</li><li>Successful completion of a technical aptitude test.</li></ul>Work EnvironmentThe position operates on the 1st shift from 7:00 am to 3:30 pm, Monday through Friday. The work environment is part of a large-scale Engineering, Repair, and Logistics company, engaging with some of the nation's largest wireless telecommunications providers. The workplace encourages maintaining a clean and organized workstation.Job Type &amp; LocationThis is a Contract to Hire position based out of West Chester, PA.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 Chester,PA.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.

RF Technician

Job Title: RF Test EngineerJob DescriptionWe are seeking a talented RF Test Engineer to join our team. You will play a crucial role in defining architecture requirements and interfaces, developing system-focused analyses for lineup analysis and link budgets, and designing test configurations. Your expertise will be essential in ensuring product verification through compliance matrices and verification reports.Responsibilities<ul><li>Define requirements and interfaces for architecture.</li><li>Develop system-focused analyses for lineup analysis and link budgets.</li><li>Design system block diagrams and evaluate test criteria.</li><li>Create test configurations and develop requirements verification compliance matrices.</li><li>Perform analysis on identified issues and manage requirements changes.</li><li>Assess system-level impacts and performance estimates.</li></ul>Essential Skills<ul><li>Experience in Production, Assembly, and Electronics.</li><li>Environmental testing expertise.</li><li>Proficiency in working on a test rack/bench for systems-level testing.</li></ul>Additional Skills &amp; Qualifications<ul><li>Ability to create architecture diagrams and requirements specification.</li><li>Proficiency in interface control documents.</li><li>Experience with analysis tools and outputs.</li><li>Skill in developing Integration &amp; Test Plans.</li><li>Capability in producing verification reports.</li></ul>Work EnvironmentYou will have the opportunity to work on a low orbiting satellite project, offering a dynamic and challenging environment.Job Type &amp; LocationThis is a Contract position based out of Los Angeles, CA.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 fully onsite position in Los Angeles,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.

RF Test Engineer

Job Title: RF Test EngineerJob DescriptionWe are seeking a talented RF Test Engineer to join our team. You will play a crucial role in defining architecture requirements and interfaces, developing system-focused analyses for lineup analysis and link budgets, and designing test configurations. Your expertise will be essential in ensuring product verification through compliance matrices and verification reports.Responsibilities<ul><li>Define requirements and interfaces for architecture.</li><li>Develop system-focused analyses for lineup analysis and link budgets.</li><li>Design system block diagrams and evaluate test criteria.</li><li>Create test configurations and develop requirements verification compliance matrices.</li><li>Perform analysis on identified issues and manage requirements changes.</li><li>Assess system-level impacts and performance estimates.</li></ul>Essential Skills<ul><li>Experience in Production, Assembly, and Electronics.</li><li>Environmental testing expertise.</li><li>Proficiency in working on a test rack/bench for systems-level testing.</li></ul>Additional Skills &amp; Qualifications<ul><li>Ability to create architecture diagrams and requirements specification.</li><li>Proficiency in interface control documents.</li><li>Experience with analysis tools and outputs.</li><li>Skill in developing Integration &amp; Test Plans.</li><li>Capability in producing verification reports.</li></ul>Work EnvironmentThe position requires working onsite five days a week in Northridge, CA. You will have the opportunity to work on a low orbiting satellite project, offering a dynamic and challenging environment.Job Type &amp; LocationThis is a Contract position based out of Los Angeles, CA.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 fully onsite position in Los Angeles,CA.Application DeadlineThis position is anticipated to close on Feb 25, 2026.<h2>About Actalent</h2>

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

Job Title: RF Test EngineerJob DescriptionWe are seeking a talented RF Test Engineer to join our team. You will play a crucial role in defining architecture requirements and interfaces, developing system-focused analyses for lineup analysis and link budgets, and designing test configurations. Your expertise will be essential in ensuring product verification through compliance matrices and verification reports.Responsibilities<ul><li>Define requirements and interfaces for architecture.</li><li>Develop system-focused analyses for lineup analysis and link budgets.</li><li>Design system block diagrams and evaluate test criteria.</li><li>Create test configurations and develop requirements verification compliance matrices.</li><li>Perform analysis on identified issues and manage requirements changes.</li><li>Assess system-level impacts and performance estimates.</li></ul>Essential Skills<ul><li>Experience in Production, Assembly, and Electronics.</li><li>Environmental testing expertise.</li><li>Proficiency in working on a test rack/bench for systems-level testing.</li></ul>Additional Skills &amp; Qualifications<ul><li>Ability to create architecture diagrams and requirements specification.</li><li>Proficiency in interface control documents.</li><li>Experience with analysis tools and outputs.</li><li>Skill in developing Integration &amp; Test Plans.</li><li>Capability in producing verification reports.</li></ul>Work EnvironmentYou will have the opportunity to work on a low orbiting satellite project, offering a dynamic and challenging environment.Job Type &amp; LocationThis is a Contract position based out of Los Angeles, CA.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 fully onsite position in Los Angeles,CA.Application DeadlineThis position is anticipated to close on Feb 25, 2026.<h2>About Actalent</h2>

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

Job Title: RF Test EngineerJob DescriptionWe are seeking a talented RF Test Engineer to join our team. You will play a crucial role in defining architecture requirements and interfaces, developing system-focused analyses for lineup analysis and link budgets, and designing test configurations. Your expertise will be essential in ensuring product verification through compliance matrices and verification reports.Responsibilities<ul><li>Define requirements and interfaces for architecture.</li><li>Develop system-focused analyses for lineup analysis and link budgets.</li><li>Design system block diagrams and evaluate test criteria.</li><li>Create test configurations and develop requirements verification compliance matrices.</li><li>Perform analysis on identified issues and manage requirements changes.</li><li>Assess system-level impacts and performance estimates.</li></ul>Essential Skills<ul><li>Experience in Production, Assembly, and Electronics.</li><li>Environmental testing expertise.</li><li>Proficiency in working on a test rack/bench for systems-level testing.</li></ul>Additional Skills &amp; Qualifications<ul><li>Ability to create architecture diagrams and requirements specification.</li><li>Proficiency in interface control documents.</li><li>Experience with analysis tools and outputs.</li><li>Skill in developing Integration &amp; Test Plans.</li><li>Capability in producing verification reports.</li></ul>Work EnvironmentYou will have the opportunity to work on a low orbiting satellite project, offering a dynamic and challenging environment.Job Type &amp; LocationThis is a Contract position based out of Los Angeles, CA.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 fully onsite position in Los Angeles,CA.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.

Job Title: RF Test EngineerJob DescriptionWe are seeking a talented RF Test Engineer to join our team. You will play a crucial role in defining architecture requirements and interfaces, developing system-focused analyses for lineup analysis and link budgets, and designing test configurations. Your expertise will be essential in ensuring product verification through compliance matrices and verification reports.Responsibilities<ul><li>Define requirements and interfaces for architecture.</li><li>Develop system-focused analyses for lineup analysis and link budgets.</li><li>Design system block diagrams and evaluate test criteria.</li><li>Create test configurations and develop requirements verification compliance matrices.</li><li>Perform analysis on identified issues and manage requirements changes.</li><li>Assess system-level impacts and performance estimates.</li></ul>Essential Skills<ul><li>Experience in Production, Assembly, and Electronics.</li><li>Environmental testing expertise.</li><li>Proficiency in working on a test rack/bench for systems-level testing.</li></ul>Additional Skills &amp; Qualifications<ul><li>Ability to create architecture diagrams and requirements specification.</li><li>Proficiency in interface control documents.</li><li>Experience with analysis tools and outputs.</li><li>Skill in developing Integration &amp; Test Plans.</li><li>Capability in producing verification reports.</li></ul>Work EnvironmentYou will have the opportunity to work on a low orbiting satellite project, offering a dynamic and challenging environment.Job Type &amp; LocationThis is a Contract position based out of Los Angeles, CA.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 fully onsite position in Los Angeles,CA.Application DeadlineThis position is anticipated to close on Feb 28, 2026.<h2>About Actalent</h2>

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

Immediate hiring for "Remote Clinical Review RN " Job Description: <ul><li>Review approximately 20 cases a day for medical necessity.</li><li>Advocate for and protect members from unnecessary hospital admissions.</li><li>Follow established procedures and processes to complete authorizations.</li><li>Collaborate with a team of nurses to assist each other and complete cases.</li><li>Communicate with doctors and case managers to make decisions and obtain additional information about members' conditions.</li><li>Utilize multiple resources to ensure the successful completion of cases.</li></ul>.Qualification :<ul><li>3+ Years of experience working with prior authorization is Mandatory</li><li>Active RN License is Mandatory</li></ul>If you are Interested , Kindly give a call : (726) 216-6069Job Type &amp; LocationThis is a Contract position based out of Austin, TX.Pay and BenefitsThe pay range for this position is $35.00 - $40.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

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

RN - Prior Authorization Nurse (Remote)

Urgent hiring for "Remote Clinical Review RN " Job Description: <ul><li>Review approximately 20 cases a day for medical necessity.</li><li>Advocate for and protect members from unnecessary hospital admissions.</li><li>Follow established procedures and processes to complete authorizations.</li><li>Collaborate with a team of nurses to assist each other and complete cases.</li><li>Communicate with doctors and case managers to make decisions and obtain additional information about members' conditions.</li><li>Utilize multiple resources to ensure the successful completion of cases.</li></ul>.Qualification :<ul><li>3+ Years of experience working with prior authorization is Mandatory</li><li>Active RN License is Mandatory</li></ul>If you are Interested , Kindly give a call : (726) 216-6069Job Type &amp; LocationThis is a Contract position based out of San Antonio, TX.Pay and BenefitsThe pay range for this position is $35.00 - $40.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

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

RN Care ManagerJob DescriptionThe RN Care Manager plays a vital role in providing clinical assessment, developing member-centered care plans, ongoing care coordination, quality assurance, and monitoring of services for program members, who may be older adults and/or individuals with intellectual or physical disabilities.Responsibilities<ul><li>Achieve member outcomes and goals through adherence to standards of care and best practices.</li><li>Interact with members and their families with the highest level of respect, compassion, and integrity.</li><li>Identify and participate in efforts to continuously improve the quality of member care and services.</li><li>Foster a member-centered culture daily.</li><li>Participate in efforts to enhance work experiences.</li><li>Actively seek and participate in training and development opportunities.</li><li>Support operational goals by adhering to operational standards and complying with contractual, regulatory, and policy requirements.</li><li>Complete discipline-specific initial and ongoing comprehensive assessments.</li><li>Conduct home visits and home assessments as needed, and consult with families and other supports for additional information.</li><li>Use critical thinking to optimize members' health and quality of life to reach goals.</li><li>Develop and maintain care plans.</li><li>Educate members and families.</li></ul>Essential Skills<ul><li>Case management</li><li>Medicare and Medicaid knowledge</li><li>Managed care experience</li><li>Healthcare industry expertise</li><li>Healthcare management systems proficiency</li><li>Care Management</li><li>RN certification</li><li>Care Plan development</li><li>Social work, psychology, and human services knowledge</li><li>Certified Functional Screener</li><li>Healthcare management</li><li>Prior authorization processes</li></ul>Additional Skills &amp; Qualifications<ul><li>RN Degree and Wisconsin License</li><li>LTC Functional Screener Certified Functional Screener</li><li>2 plus years of Care Management Experience</li></ul>Work EnvironmentThe RN Care Manager will manage their schedule based on members' needs, primarily working day shift hours. The role requires in-home and/or LTC Facility visits with members. While remote work is possible, access to an office is required for training and internal meetings. Training will generally occur in the office for the first 3-6 months, after which more remote work is possible. Staff are generally asked to be in the office three days per week. Training and orientation will be held in Milwaukee at the Vliet Location, with reimbursement for mileage.Job Type &amp; LocationThis is a Contract to Hire position based out of Sheboygan, WI.Pay and BenefitsThe pay range for this position is $32.69 - $38.46/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 Sheboygan,WI.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.

RN Care Manager

Job Title: RN Care ManagerJob DescriptionThe RN Care Manager plays a vital role in providing clinical assessment, developing member-centered care plans, ongoing care coordination, quality assurance, and monitoring of services for program members, who may be older adults and/or individuals with intellectual or physical disabilities.Responsibilities<ul><li>Achieve member outcomes and goals through adherence to standards of care and best practices.</li><li>Interact with members and their families with the highest level of respect, compassion, and integrity.</li><li>Identify and participate in efforts to continuously improve the quality of member care and services.</li><li>Foster a member-centered culture daily.</li><li>Participate in efforts to enhance work experiences.</li><li>Actively seek and participate in training and development opportunities.</li><li>Support operational goals by adhering to operational standards and complying with contractual, regulatory, and policy requirements.</li><li>Complete discipline-specific initial and ongoing comprehensive assessments.</li><li>Conduct home visits and home assessments as needed, and consult with families and other supports for additional information.</li><li>Use critical thinking to optimize members' health and quality of life to reach goals.</li><li>Develop and maintain care plans.</li><li>Educate members and families.</li></ul>Essential Skills<ul><li>Case management</li><li>Medicare and Medicaid knowledge</li><li>Managed care experience</li><li>Healthcare industry expertise</li><li>Healthcare management systems proficiency</li><li>Care Management</li><li>RN certification</li><li>Care Plan development</li><li>Social work, psychology, and human services knowledge</li><li>Certified Functional Screener</li><li>Healthcare management</li><li>Prior authorization processes</li></ul>Additional Skills &amp; Qualifications<ul><li>LPN or RN Degree and Wisconsin License</li><li>LTC Functional Screener Certified Functional Screener</li><li>2 plus years of Care Management Experience</li></ul>Work EnvironmentThe RN Care Manager will manage their schedule based on members' needs, primarily working day shift hours. The role requires in-home and/or LTC Facility visits with members. While remote work is possible, access to an office is required for training and internal meetings. Training will generally occur in the office for the first 3-6 months, after which more remote work is possible. Staff are generally asked to be in the office three days per week. Training and orientation will be held in Milwaukee at the Vliet Location, with reimbursement for mileage.Job Type &amp; LocationThis is a Contract to Hire position based out of Sheboygan, WI.Pay and BenefitsThe pay range for this position is $32.69 - $38.46/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 Sheboygan,WI.Application DeadlineThis position is anticipated to close on Feb 23, 2026.<h2>About Actalent</h2>

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

Job Title: RN Case ManagerJob DescriptionThe RN Case Manager will be an integral part of the PACE program, performing assessments and coordinating interdisciplinary care for participants. You will participate in developing care plans and collaborate with the Utilization Management Committee to ensure comprehensive care delivery.Responsibilities<ul><li>Conduct initial RN assessments for PACE participants.</li><li>Coordinate care for a caseload of PACE participants, ensuring skilled services are delivered as needed.</li><li>Document care delivery, care coordination, and interdisciplinary team (IDT) care planning.</li><li>Develop viable discharge plans in collaboration with patients and their families.</li><li>Support patients throughout the service area, ensuring access to necessary services.</li></ul>Essential Skills<ul><li>Minimum of 2 years of acute care case management experience, ideally 5+ years.</li><li>Active and unencumbered California RN license.</li><li>Certification in Basic Life Support (BLS) from the American Heart Association.</li><li>Knowledge of case and utilization management practices and methodologies.</li><li>Understanding of state and federal healthcare regulations and accreditation.</li></ul>Additional Skills &amp; Qualifications<ul><li>Home Health experience is a plus.</li><li>Travel experience is not required.</li><li>Nationally recognized certification in Utilization Management or Case Management preferred.</li><li>Minimum of two years inpatient acute care experience required.</li><li>Minimum of one year of Hospital Case Management or Hospital Utilization Management experience.</li></ul>Work EnvironmentThe position is based in the PACE Clinic setting, part of a long-term care model designed to help older adults stay independent and safe in their own homes. This comprehensive care program for seniors with complex medical needs provides services through a coordinated organization, managing everything from primary care to transportation. The program has expanded significantly, serving over 350 participants, emphasizing continual learning and development within a large academic medical center recognized for its excellence and Magnet status.Job Type &amp; LocationThis is a Contract position based out of Loma Linda, CA.Pay and BenefitsThe pay range for this position is $50.00 - $70.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Loma Linda,CA.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.

RN Case Manager

Job Title: RN Case ManagerJob DescriptionThe RN Case Manager will be an integral part of the PACE program, performing assessments and coordinating interdisciplinary care for participants. You will participate in developing care plans and collaborate with the Utilization Management Committee to ensure comprehensive care delivery.Responsibilities<ul><li>Conduct initial RN assessments for PACE participants.</li><li>Coordinate care for a caseload of PACE participants, ensuring skilled services are delivered as needed.</li><li>Document care delivery, care coordination, and interdisciplinary team (IDT) care planning.</li><li>Develop viable discharge plans in collaboration with patients and their families.</li><li>Support patients throughout the service area, ensuring access to necessary services.</li></ul>Essential Skills<ul><li>Minimum of 2 years of acute care case management experience, ideally 5+ years.</li><li>Active and unencumbered California RN license.</li><li>Certification in Basic Life Support (BLS) from the American Heart Association.</li><li>Knowledge of case and utilization management practices and methodologies.</li><li>Understanding of state and federal healthcare regulations and accreditation.</li></ul>Additional Skills &amp; Qualifications<ul><li>Home Health experience is a plus.</li><li>Travel experience is not required.</li><li>Nationally recognized certification in Utilization Management or Case Management preferred.</li><li>Minimum of two years inpatient acute care experience required.</li><li>Minimum of one year of Hospital Case Management or Hospital Utilization Management experience.</li></ul>Work EnvironmentThe position is based in the PACE Clinic setting, part of a long-term care model designed to help older adults stay independent and safe in their own homes. This comprehensive care program for seniors with complex medical needs provides services through a coordinated organization, managing everything from primary care to transportation. The program has expanded significantly, serving over 350 participants, emphasizing continual learning and development within a large academic medical center recognized for its excellence and Magnet status.Job Type &amp; LocationThis is a Contract position based out of Loma Linda, CA.Pay and BenefitsThe pay range for this position is $50.00 - $70.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Loma Linda,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.

Job Title: RN Case ManagerJob DescriptionThe RN Case Manager plays a crucial role in the patient care delivery team within a level one trauma designation, ST-Elevation Myocardial Infarction (STEMI) receiving center, and Comprehensive Stroke and Chest Pain Center. This role requires the use of clinical expertise and independent judgment to perform the nursing process, including assessment, care planning, intervention, and evaluation, within a patient-centered care professional practice model.Responsibilities<ul><li>Work efficiently in a fast-paced environment, utilizing clinical expertise in case management functions.</li><li>Maintain a solid working knowledge of case and utilization management methodologies.</li><li>Ensure medical appropriateness criteria are met and documented from admission through discharge.</li><li>Collaborate in a healthcare environment to implement an interdisciplinary plan of care with a comprehensive discharge plan.</li><li>Reevaluate the plan of care based on the patient's changing needs and condition.</li><li>Exhibit a positive mindset with changes in the workforce, clinical practice, and operational setting.</li><li>Engage in opportunities to influence decision-making for bedside clinical practice.</li><li>Work calmly and respond courteously under pressure.</li></ul>Essential Skills<ul><li>Minimum of 2 years of acute inpatient experience.</li><li>Experience in trauma level 1 hospital discharge planning.</li><li>RN license with active and unencumbered California RN license.</li><li>Active BLS certification from the American Heart Association.</li><li>Bachelor’s degree in nursing.</li><li>Minimum of two years inpatient acute care experience.</li><li>Minimum of one year of hospital case management or hospital utilization management experience.</li></ul>Additional Skills &amp; Qualifications<ul><li>Nationally recognized certification in Utilization Management or Case Management preferred.</li><li>Knowledge of state and federal healthcare regulations and accreditation.</li></ul>Work EnvironmentThis role offers the opportunity to work at a Magnet Recognized large tertiary academic medical center, which emphasizes continual learning and development. The case management team is extensive, providing substantial career-pathing opportunities. You will be working in a 400-bed, level one trauma acute setting. The position requires working every other weekend, and shifts are conducted within a collaborative and supportive healthcare environment.Job Type &amp; LocationThis is a Contract position based out of Loma Linda, CA.Pay and BenefitsThe pay range for this position is $50.00 - $70.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Loma Linda,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.

Job Title: Field EngineerJob DescriptionJoin a dynamic team leading the deployment and replacement of civil air traffic surveillance radars—both approach and en-route—across the United States. As a Field Engineer, you will play a key role in delivering advanced radar solutions that enhance the safety and efficiency of air traffic nationwide.Responsibilities<ul><li>Lead the definition of system architecture and analyze functional and technical requirements for large-scale radar deployments.</li><li>Design and document technical interfaces, ensuring seamless integration of all components, including COTS (commercial off-the-shelf) and third-party systems.</li><li>Coordinate and drive internal and formal technical reviews, maintaining the highest standards of quality and compliance.</li><li>Prepare essential technical documentation, such as Interface Control Documents (ICD) and System Test Plans (TP), in collaboration with the Product Department.</li><li>Oversee and approve partial deliverables throughout all project phases, working closely with Field Engineering teams.</li><li>Ensure successful delivery and integration of radar systems at multiple sites distributed across the United States.</li><li>Foster collaboration with the System Engineering organization and other multidisciplinary teams to guarantee project success.</li><li>Maintain clear and effective communication with all stakeholders, proactively resolving issues and promoting continuous improvement.</li></ul>Essential Skills<ul><li>2-3+ years of experience in field engineering or systems engineering.</li><li>Customer service and technical support experience.</li><li>Proficiency in electrical and radar systems.</li><li>Experience or exposure to radars, air surveillance, or air traffic equipment.</li><li>Product support and electronics knowledge.</li><li>Experience with FAA, aerospace defense, air traffic, and air surveillance.</li></ul>Additional Skills &amp; Qualifications<ul><li>3-5+ years of experience in field engineering, systems engineering, technical management, and project management within radar, air traffic surveillance, or similar sectors.</li><li>Bachelor's degree or higher preferred (Technical or Engineering Degree).</li><li>Strong organizational, analytical, and problem-solving skills.</li><li>Ability to work effectively in cross-functional and geographically distributed teams.</li></ul>Work EnvironmentThis role involves traveling up to 30-50% of the time, generally closer to 30%. The company is in a growth phase, planning to double in size over the next year and again in the next five years. The team will move into a brand-new facility in the next six months, with phases of expansion occurring consistently across the US.Job Type &amp; LocationThis is a Contract to Hire position based out of Overland Park, KS.Pay and BenefitsThe pay range for this position is $38.46 - $43.27/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 Overland Park,KS.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.

Radar/Avionics Field Engineer

Job Title: Radiologic TechnologistJob DescriptionAs a Radiologic Technologist, you will perform all routine diagnostic and therapeutic radiographic procedures, ensuring the production of high-quality images with minimal repeats. You will apply radiation and physical safety measures, calculate appropriate exposure factors, and evaluate images for diagnostic quality. Your role includes explaining procedures and observing patients to ensure safety and comfort during exams.Responsibilities<ul><li>Perform routine diagnostic and therapeutic radiographic procedures.</li><li>Produce high-quality images with minimal repeats while applying safety measures.</li><li>Calculate appropriate exposure factors and evaluate images for diagnostic quality.</li><li>Explain procedures to patients and ensure their safety and comfort during exams.</li><li>Demonstrate knowledge of contrast media injections and monitor for reactions.</li><li>Oversee duties assigned to student radiographers.</li><li>Handle telephone scheduling procedures.</li><li>Operate the PACS computer system.</li></ul>Essential Skills<ul><li>Radiology</li><li>Radiologic Technology</li><li>Imaging</li></ul>Additional Skills &amp; Qualifications<ul><li>Graduate of an accredited two-year Radiologic Technology training program approved by the Council of Medical Education of the AMA.</li><li>Registered or registry eligible with the ARRT.</li><li>Basic Life Support certification.</li></ul>Work EnvironmentYou will work in a 656-bed hospital that includes specialized centers such as The Alexander Burn Center, The Peggy V. Helmerich Women’s Health Center, and the Oklahoma Heart Institute. The schedule is Monday through Friday, 7:00 AM - 3:30 PM. The hospital is open to training in specialties and other modalities, offering a great opportunity for those looking to specialize further. We thrive in a people-first environment, offering career growth opportunities, tuition assistance, and a supportive, inclusive culture with comprehensive health benefits and paid time off. Our advanced technology supports our team and enhances patient care.Job Type &amp; LocationThis is a Permanent position based out of Tulsa, OK.Pay and BenefitsThe pay range for this position is $60000.00 - $70000.00/yr.Company benefits - active first day of the month after 30 days of employmentWorkplace TypeThis is a fully onsite position in Tulsa,OK.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.

Radiologic Technologist

Job Title: Lab TechnologistJob DescriptionWe are seeking a dedicated Lab Technologist to perform equipment and instrument set-up according to established procedures. This role requires the ability to manage all necessary documentation and deliver high-quality patient care independently and without supervision. The main shift is a 4-day schedule with 10-hour shifts.Responsibilities<ul><li>Process and manage all necessary documentation</li><li>Deliver high-quality patient care and ensure patient safety</li></ul>Essential Skills<ul><li>BLS Certification</li><li>At least 5+ years of experience as a Technologist, preferably in a hospital setting</li></ul>Additional Skills &amp; Qualifications<ul><li>OR experience is advantageous</li><li>Must possess excellent patient care skills</li></ul>Work EnvironmentThe work schedule consists of 10-hour shifts with variable start times at 0700 and end times at 1730. There is an on-call requirement after weekday shifts until the next morning at 0700, occurring 3 times per week. Weekend on-call duties are 24 hours from Saturday 0700 to Sunday 0700 and/or Sunday 0700 to Monday 0700. The contract duration is 13 weeks. The organization provides a Christian-focused, service-oriented environment emphasizing compassion, integrity, humility, and teamwork. If converted to a full-time employee, benefits include comprehensive health coverage with no-deductible options, strong retirement matching, and an emphasis on employee spiritual and physical health through the Employee Wholeness program. Opportunities for career advancement exist within this prestigious, award-winning academic medical system.Job Type &amp; LocationThis is a Contract position based out of Murrieta, CA.Pay and BenefitsThe pay range for this position is $50.00 - $60.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Murrieta,CA.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.

<h1>Job Title: Radiology Technologist</h1><h2>Job Description</h2>Perform radiographic procedures by operating equipment using ionizing radiation according to established procedures and under the direction of a radiologist. Process all documentation and perform all duties independently and without supervision.<h2>Responsibilities</h2><ul><li>Operate radiographic equipment using ionizing radiation.</li><li>Perform radiographic procedures as directed by a radiologist.</li><li>Ensure all documentation is processed accurately and promptly.</li><li>Provide patient care in accordance with established protocols.</li><li>Maintain a safe and clean work environment.</li></ul><h2>Essential Skills</h2><ul><li>Basic Life Support (BLS) certification.</li><li>Experience with Radiology, X-ray, Phillips C-ARM, and FUJI Portable X-ray.</li><li>OR experience and patient care skills.</li><li>ARRT Certification.</li><li>Diagnostic Radiologic Technology Certificate (CRT).</li><li>California permit in Radiologic Technology and Fluoroscopy.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Fully Licensed X-Ray Tech (CRT) with Fluoroscopy Permit.</li><li>BLS-AHA Certified.</li></ul>Work EnvironmentMid Shift 3 pm – 11:30 pm (+every other weekend) *Occasional Graveyard shift as needed. The work environment is located in the cities of Covina, Glendora, and West Covina in the East San Gabriel Valley, known for being a great place to work. This is a contract position based out of West Covina, California. The work environment is dynamic, with facilities recognized as a 'Best Place to Work' in 2021.Job Type &amp; LocationThis is a Contract position based out of West Covina, CA.Pay and BenefitsThe pay range for this position is $37.71 - $56.57/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 Covina,CA.Application DeadlineThis position is anticipated to close on Feb 21, 2026.<h2>About Actalent</h2>

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

Radiologic Technologist (Full Time PM Shift)

<h1>Job Title: Radiology Technologist</h1><h2>Job Description</h2>Perform radiographic procedures by operating equipment using ionizing radiation according to established procedures and under the direction of a radiologist. Process all documentation and perform all duties independently and without supervision.<h2>Responsibilities</h2><ul><li>Operate radiographic equipment using ionizing radiation.</li><li>Perform radiographic procedures as directed by a radiologist.</li><li>Ensure all documentation is processed accurately and promptly.</li><li>Provide patient care in accordance with established protocols.</li><li>Maintain a safe and clean work environment.</li></ul><h2>Essential Skills</h2><ul><li>Basic Life Support (BLS) certification.</li><li>Experience with Radiology, X-ray, Phillips C-ARM, and FUJI Portable X-ray.</li><li>OR experience and patient care skills.</li><li>ARRT Certification.</li><li>Diagnostic Radiologic Technology Certificate (CRT).</li><li>California permit in Radiologic Technology and Fluoroscopy.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Fully Licensed X-Ray Tech (CRT) with Fluoroscopy Permit.</li><li>BLS-AHA Certified.</li></ul>Work EnvironmentMid Shift 3 pm – 11:30 pm (+every other weekend) *Occasional Graveyard shift as needed. The work environment is located in the cities of Covina, Glendora, and West Covina in the East San Gabriel Valley, known for being a great place to work. This is a contract position based out of West Covina, California. The work environment is dynamic, with facilities recognized as a 'Best Place to Work' in 2021.Job Type &amp; LocationThis is a Contract position based out of West Covina, CA.Pay and BenefitsThe pay range for this position is $37.71 - $56.57/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 Covina,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.

Radiologic Technologist (Full Time)

<h2>Job Title: Radiology Technologist</h2>Job Description:We are seeking a dedicated Radiology Technologist. This role requires the ability to manage all necessary duties and deliver high-quality patient care independently and without supervision. The main shift is a 4-day schedule with 10-hour shifts.Responsibilities<ul><li>Operate radiographic equipment</li><li>Perform radiographic procedures as directed by a radiologist.</li><li>Ensure all documentation is processed accurately and promptly.</li><li>Provide patient care in accordance with established protocols.</li><li>Maintain a safe and clean work environment.</li></ul>Essential Skills<ul><li>Basic Life Support (BLS) certification.</li><li>5+ years of experience as a Radiology Technologist</li><li>OR experience and patient care skills.</li><li>ARRT Certification.</li><li>Diagnostic Radiologic Technology Certificate (CRT).</li><li>California permit in Radiologic Technology and Fluoroscopy.</li></ul>Additional Skills &amp; Qualifications<ul><li>BLS-AHA Certified.</li><li>Must possess excellent patient care skills</li></ul>Work EnvironmentThe work schedule consists of 10-hour shifts with variable start times at 0700 and end times at 1730. There is an on-call requirement after weekday shifts until the next morning at 0700, occurring 3 times per week. Weekend on-call duties are 24 hours from Saturday 0700 to Sunday 0700 and/or Sunday 0700 to Monday 0700. The contract duration is 13 weeks. The organization provides a Christian-focused, service-oriented environment emphasizing compassion, integrity, humility, and teamwork. If converted to a full-time employee, benefits include comprehensive health coverage with no-deductible options, strong retirement matching, and an emphasis on employee spiritual and physical health through the Employee Wholeness program. Opportunities for career advancement exist within this prestigious, award-winning academic medical system.Job Type &amp; LocationThis is a Contract position based out of Murrieta, CA.Pay and BenefitsThe pay range for this position is $50.00 - $60.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Murrieta,CA.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.

Radiology Technologist

As a Regional Clinical Trial Manager, you will oversee the day-to-day operations of clinical trials within your designated region, ensuring compliance with protocols, ICH GCP, and regulatory requirements. You will work closely with CRO partners, study vendors, and cross-functional team members to ensure successful trial execution, leading activities that promote quality, consistency, and cross-functional alignment.Responsibilities<ul><li>Manage clinical trials in LATAM (Brazil and Argentina), overseeing CRO vendors and other study vendors.</li><li>Ensure timely shipments of vendor supplies to LATAM sites, including Central Lab kits.</li><li>Manage study budgets, timelines, and metrics, ensuring adherence.</li><li>Oversee Study Start-Up activities, site selection, activation timelines, and contract negotiations.</li><li>Serve as the primary escalation point for regional and site-related issues.</li><li>Participate in weekly meetings with CRO partners and study vendors, ensuring cross-functional alignment.</li><li>Review study-related clinical plans and documents.</li><li>Perform quality and monitoring oversight activities, ensuring audit-ready condition of clinical trial documentation.</li><li>Conduct Monitoring Oversight visits to assess compliance, as required.</li><li>Oversee participant recruitment and retention strategies.</li><li>Coordinate regulatory and ethics committee submission activities, ensuring compliance with local regulatory requirements.</li><li>Assist with Investigator and Site Initiation visits.</li></ul>Essential Skills<ul><li>Bachelor's degree in Life Sciences, Nursing, or equivalent.</li><li>Minimum 5 years of experience in Clinical Operations.</li><li>Minimum 3 years of experience in clinical study management.</li><li>Hands-on experience managing studies in LATAM.</li><li>Spanish and/or Portuguese speaking is preferred.</li></ul>Additional Skills &amp; Qualifications<ul><li>Ph.D. in a related life science discipline is preferred.</li><li>Operational experience managing at least two studies as a regional CTM for LATAM.</li><li>Knowledge of regulatory requirements in Brazil.</li><li>Ability to travel approximately 20% of the time to LATAM.</li></ul>Work EnvironmentThis is a remote role, with a preference for candidates located on the east coast. The position requires the ability to travel approximately 20% of the time, particularly to Brazil and Argentina.Job Type &amp; LocationThis is a Contract position based out of Boston, MA.Pay and BenefitsThe pay range for this position is $70.00 - $70.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

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

Regional Clinical Trial Manager

As a Regional Clinical Trial Manager, you will oversee the day-to-day operations of clinical trials within your designated region, ensuring compliance with protocols, ICH GCP, and regulatory requirements. You will work closely with CRO partners, study vendors, and cross-functional team members to ensure successful trial execution, leading activities that promote quality, consistency, and cross-functional alignment.Responsibilities<ul><li>Manage clinical trials in LATAM (Brazil and Argentina), overseeing CRO vendors and other study vendors.</li><li>Ensure timely shipments of vendor supplies to LATAM sites, including Central Lab kits.</li><li>Manage study budgets, timelines, and metrics, ensuring adherence.</li><li>Oversee Study Start-Up activities, site selection, activation timelines, and contract negotiations.</li><li>Serve as the primary escalation point for regional and site-related issues.</li><li>Participate in weekly meetings with CRO partners and study vendors, ensuring cross-functional alignment.</li><li>Review study-related clinical plans and documents.</li><li>Perform quality and monitoring oversight activities, ensuring audit-ready condition of clinical trial documentation.</li><li>Conduct Monitoring Oversight visits to assess compliance, as required.</li><li>Oversee participant recruitment and retention strategies.</li><li>Coordinate regulatory and ethics committee submission activities, ensuring compliance with local regulatory requirements.</li><li>Assist with Investigator and Site Initiation visits.</li></ul>Essential Skills<ul><li>Bachelor's degree in Life Sciences, Nursing, or equivalent.</li><li>Minimum 5 years of experience in Clinical Operations.</li><li>Minimum 3 years of experience in clinical study management.</li><li>Hands-on experience managing studies in LATAM.</li><li>Spanish and/or Portuguese speaking is preferred.</li></ul>Additional Skills &amp; Qualifications<ul><li>Ph.D. in a related life science discipline is preferred.</li><li>Operational experience managing at least two studies as a regional CTM for LATAM.</li><li>Knowledge of regulatory requirements in Brazil.</li><li>Ability to travel approximately 20% of the time to LATAM.</li></ul>Work EnvironmentThis is a remote role, with a preference for candidates located on the east coast. The position requires the ability to travel approximately 20% of the time, particularly to Brazil and Argentina.Job Type &amp; LocationThis is a Contract position based out of Parsippany-Troy Hills, NJ.Pay and BenefitsThe pay range for this position is $70.00 - $70.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

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

ARCHITECT- direct hire opportunitiesDescriptionSeeking a talented Architect to join our multi-discipline project team to support the programming, conceptual development, design, and construction document preparation of facility-related projects from conception through construction.Key responsibilities include project scope development, design and creation of visual representations, design drawings, writing specifications, and assisting with construction administration services. Meetings and communication with clients as well as within a design team working remotely or in other offices occur daily throughout the span of projects. QualificationsA degree in architecture is required along with 5+ years of experienceProfessional registration or the ability to become licensed as a Registered Architect in Michigan is requiredPreferred candidates will have experience working with Revit softwareExperience in AutoCAD is a plusCandidates should have a successful work history collaborating with other consultants, owners, and contractors on projects using various project delivery methodsLEED accreditation is a plus as is experience working with commercial, industrial, healthcare, multi-family and municipal projectsThe candidate must have excellent communication skills and be able to work in a team environmentSkillsRevit, Architecture, Construction document, Autocad, Design, Construction administration, Architectural design, Project management, Sketchup, Design development, Drafting, Retail, Revit architecture, Health care, Mixed use, Registered architect, Licensed Architect, Multi-FamilyTop Skills DetailsRevit,Architecture,Construction document,Autocad,Design,Construction administration,Architectural design,Project management,Sketchup,Design development,Drafting,Retail,Revit architecture,Health care,Mixed use,Registered architect,Additional Skills &amp; QualificationsMust Haves:- Bachelor Degree in Architecture - Proficient in Revit or AutoCAD- Licensed/Registered- Architecture experience within Commercial Buildings, Mixed-Use, Industrial, or MuncipalExperience LevelIntermediate LevelJob Type &amp; LocationThis is a Permanent position based out of Saginaw, MI.Pay and BenefitsThe pay range for this position is $35.00 - $52.00/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 Saginaw,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.

Registed Architect

Job Title: Registered NurseJob DescriptionWe are seeking a dedicated Registered Nurse to facilitate patient care, manage electronic medical records, and triage phone calls for nurse-related questions. The role involves coordinating follow-up on patient care, reviewing imaging orders, biopsies, medication reviews, and conducting nurse visits in the office. You will be responsible for organizing medications for doctors, updating EMR, and handling prescription refills.Responsibilities<ul><li>Employ appropriate and timely use of Tasking in EHR.</li><li>Maintain efficient patient flow.</li><li>Function as the liaison between patients, staff, and physicians.</li><li>Assure all patients are correctly identified prior to providing and/or documenting care.</li><li>Ensure proper preparation for patient visits and prepare pertinent information needed.</li><li>Provide referrals and consult orders appropriately and in a timely manner in the PMS and EHR.</li><li>Check and maintain logs for emergency equipment according to policy.</li><li>Collect lab specimens according to departmental guidelines and accurately label specimens.</li><li>Demonstrate telephone triage protocols and document in EHR.</li><li>Schedule appointments appropriately and accurately according to department guidelines.</li><li>Review and update medication lists in EHR, demonstrating understanding of prescription control and prescription refill procedures.</li><li>Accurately document known allergies in EHR.</li><li>Enter orders and schedule appointments in the Practice Management System (PMS) and EHR.</li></ul>Essential Skills<ul><li>Active NJ State Nursing License</li><li>Experience with EMR systems (Athena or Epic preferred)</li><li>Patient care skills</li><li>RN license</li><li>Associates degree required, BSN preferred</li><li>Experience in Orthopedic, Pain management, Podiatry, or Muscular/Skeletal settings</li></ul>Additional Skills &amp; Qualifications<ul><li>Outpatient experience is nice to have</li><li>Experience in primary care or hospital facility</li><li>Experience with triage and healthcare protocols</li></ul>Work EnvironmentThe work environment is supportive, with a team of staff and providers dedicated to patient care. The role involves building long-term relationships with patients, seeing them quarterly or biannually. Working hours are Monday to Friday with rotations of 7:30-4, 8-4:30, and 8:30-5:00, including six Saturdays a year. Physical requirements include pushing, pulling, lifting heavy objects, physical mobility and agility, dexterity, balance, and endurance.Job Type &amp; LocationThis is a Contract to Hire position based out of Florham Park, NJ.Pay and BenefitsThe pay range for this position is $38.00 - $50.00/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 Florham Park,NJ.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.

Registered Nurse

Job Title: Registered NurseJob DescriptionWe are seeking a dedicated Registered Nurse to facilitate patient care, manage electronic medical records, and triage phone calls for nurse-related questions. The role involves coordinating follow-up on patient care, reviewing imaging orders, biopsies, medication reviews, and conducting nurse visits in the office. You will be responsible for organizing medications for doctors, updating EMR, and handling prescription refills.Responsibilities<ul><li>Employ appropriate and timely use of Tasking in EHR.</li><li>Maintain efficient patient flow.</li><li>Function as the liaison between patients, staff, and physicians.</li><li>Assure all patients are correctly identified prior to providing and/or documenting care.</li><li>Ensure proper preparation for patient visits and prepare pertinent information needed.</li><li>Provide referrals and consult orders appropriately and in a timely manner in the PMS and EHR.</li><li>Check and maintain logs for emergency equipment according to policy.</li><li>Collect lab specimens according to departmental guidelines and accurately label specimens.</li><li>Demonstrate telephone triage protocols and document in EHR.</li><li>Schedule appointments appropriately and accurately according to department guidelines.</li><li>Review and update medication lists in EHR, demonstrating understanding of prescription control and prescription refill procedures.</li><li>Accurately document known allergies in EHR.</li><li>Enter orders and schedule appointments in the Practice Management System (PMS) and EHR.</li></ul>Essential Skills<ul><li>Active NJ State Nursing License</li><li>Experience with EMR systems (Athena or Epic preferred)</li><li>Patient care skills</li><li>RN license</li><li>Associates degree required, BSN preferred</li><li>Experience in Orthopedic, Pain management, Podiatry, or Muscular/Skeletal settings</li></ul>Additional Skills &amp; Qualifications<ul><li>Outpatient experience is nice to have</li><li>Experience in primary care or hospital facility</li><li>Experience with triage and healthcare protocols</li></ul>Work EnvironmentThe work environment is supportive, with a team of staff and providers dedicated to patient care. The role involves building long-term relationships with patients, seeing them quarterly or biannually. Working hours are Monday to Friday with rotations of 7:30-4, 8-4:30, and 8:30-5:00, including six Saturdays a year. Physical requirements include pushing, pulling, lifting heavy objects, physical mobility and agility, dexterity, balance, and endurance.Job Type &amp; LocationThis is a Contract to Hire position based out of Florham Park, NJ.Pay and BenefitsThe pay range for this position is $38.00 - $50.00/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 Florham Park,NJ.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.

Actalent is looking for a registered nurse located in Odessa to support an Oncology clinic.Schedule: Monday–Friday, 8:30 AM–5:00 PMCompensation: $35–$45 per hour (based on experience)Overview: Our oncology clinic in Odessa is seeking a compassionate and skilled Infusion Nurse to join our care team. This role focuses on providing high‑quality infusion services to oncology patients in a supportive outpatient environment. The ideal candidate is detail‑oriented, patient‑focused, and comfortable working in a fast‑paced clinical setting.Key responsibilities:<ul><li>Administer chemotherapy, immunotherapy, and other IV infusions in accordance with provider orders and safety protocols</li><li>Monitor patients for infusion reactions and provide appropriate interventions</li><li>Perform venipuncture, access ports, and maintain central lines</li><li>Document all treatments, assessments, and patient interactions accurately in the EMR</li><li>Collaborate with oncologists, nurse practitioners, and support staff to ensure coordinated patient care</li><li>Educate patients and families on treatment plans, side effects, and post‑infusion care</li><li>Maintain a clean, safe, and compliant infusion environment</li><li>Follow all OSHA, HIPAA, and oncology‑specific safety standards</li></ul>Qualifications:<ul><li>Active RN license in the state of Texas</li><li>Previous infusion or oncology experience preferred (but strong IV skills may be considered)</li><li>OCN certification is a plus</li><li>Strong assessment and critical‑thinking skills</li><li>Excellent communication and patient‑care abilities</li></ul>If you are interested in this position, please apply today! Only one spot available. Job Type &amp; LocationThis is a Contract to Hire position based out of Odessa, TX.Pay and BenefitsThe pay range for this position is $35.00 - $45.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

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

Infusion Registered Nurse (RN) — Odessa, TXSchedule: Monday–Friday only, normal business hoursPay &amp; Benefits: Competitive pay + full benefitsJoin a reputable outpatient infusion setting in Odessa, TX, providing compassionate, high‑quality patient care in a predictable weekday schedule.<h3>Key Responsibilities</h3><ul><li>Administer IV therapies, medications, and blood products with accuracy and safety.</li><li>Perform venipuncture, access ports, and manage central line care.</li><li>Assess patients, review labs, and collaborate with physicians on dose modifications.</li><li>Educate patients and families on treatments and care instructions.</li><li>Maintain thorough clinical documentation.</li></ul><h3>Qualifications</h3><ul><li>Current RN license in the state of Texas.</li><li>0–3+ years of RN experience (all levels considered).</li><li>BLS certification required.</li><li>BSN preferred.</li></ul><h3>Why This Role</h3><ul><li>Monday–Friday schedule — no weekends.</li><li>Strong compensation and great benefits package.</li><li>Stable, professional outpatient environment.</li></ul>Apply today to be considered for this opportunity in Odessa, TX.Job Type &amp; LocationThis is a Contract to Hire position based out of Odessa, TX.Pay and BenefitsThe pay range for this position is $35.00 - $45.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Odessa,TX.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: Pharmacy TechnicianJob DescriptionWe are seeking a dedicated Pharmacy Technician to join our fulfillment team. In this role, you will be responsible for back-end operations, which include packaging, scanning prescriptions, and loading medicines into automated dispensing machines. This position requires standing on your feet during 8-hour shifts.Responsibilities<ul><li>Package and scan prescriptions accurately.</li><li>Load medicines into automated dispensing machines.</li><li>Ensure all order entries are completed promptly and accurately.</li><li>Assist in the fulfillment process to maintain efficient pharmacy operations.</li></ul>Essential Skills<ul><li>Pharmacy technician license (CPhT preferred).</li><li>Proficiency in pharmacy order entry and fulfillment.</li><li>Strong data entry and computer skills.</li><li>Experience in retail pharmacy and specialty pharmacy operations.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience with insurance processes.</li><li>Ability to lift up to 25 lbs.</li><li>Registered Pharmacy Technician certification.</li><li>Previous experience in a retail pharmacy setting.</li></ul>Work EnvironmentThis position operates within a closed-door dispensing pharmacy environment. Employees must be comfortable standing for 8-hour shifts, Monday through Friday, with some weekend shifts possible. The role offers a hybrid work schedule, promotional opportunities, and internal benefits, including holiday and PTO.Job Type &amp; LocationThis is a Contract to Hire position based out of Lakeland, FL.Pay and BenefitsThe pay range for this position is $17.00 - $17.00/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 Lakeland,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.

Registered Pharmacy Technician

Job Title: Regulatory AssociateShift: M-F (8am-5pm)Job DescriptionThe Regulatory Associate is responsible for supporting the team in managing the product lifecycle management system. This includes creating specifications and verifying supplier documents, managing customer information requests, developing nutritional fact labels, and ensuring compliance with emerging regulations.Responsibilities<ul><li>Ensure the product lifecycle system is up to date.</li><li>Create and update specifications for new product rollouts and compliance with changing customer needs.</li><li>Support the change management and approval/communication process.</li><li>Ensure that specifications content accurately addresses regulatory, customer, and company needs.</li><li>Demonstrate proficiency in Genesis ESHA labeling software system to support product development and maintain accurate ingredient information.</li><li>Work with customers, sales, and facility quality assurance personnel to complete and accurately fulfill customer information requests.</li><li>Prioritize workload to achieve on-time completion of deliverables.</li><li>Verify supplier/material documentation supporting the product lifecycle management system.</li></ul>Qualifications<ul><li>Bachelor's degree in food science, nutrition, or related science field.</li><li>2 years of experience within the food industry.</li><li>Experience in creating specifications and verification documents in quality.</li><li>Experience working directly with customers on their specifications and managing the product lifecycle.</li><li>Experience ensuring customer specifications align with regulatory needs.</li><li>Knowledge in nutritional labeling and compliance, quality assurance, and regulatory affairs﻿</li></ul>Job Type &amp; LocationThis is a Contract position based out of Bartlett, IL.Pay and BenefitsThe pay range for this position is $27.85 - $33.50/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 Bartlett,IL.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.

Regulatory Affairs Associate

Job Title: Regulatory Affairs SpecialistJob DescriptionThe Regulatory Affairs Specialist plays a crucial role in supporting US FDA applications (NDAs, ANDAs, DMFs) and international drug product applications. This position involves planning, authoring, compiling, and submitting statutory reports in eCTD format for marketed products according to FDA requirements. The role also includes reviewing and assessing CMC regulatory impacts of post-approval changes and providing regulatory strategies.Responsibilities<ul><li>Plan, author, compile, and submit statutory reports in eCTD format for marketed products per FDA requirements.</li><li>Review and assess CMC regulatory impact of post-approval changes proposed at the manufacturing site and provide regulatory strategy.</li><li>Plan, author, compile, submit, and manage variations and supplements for marketed products within and outside the United States.</li><li>Participate in cross-functional teams and provide health authority requirements needed for support of post-approval changes.</li><li>Author and review updates to marketed product labeling.</li><li>Maintain regulatory knowledge of current guidelines and regulations.</li><li>Maintain current regulatory databases and produce various reports as needed.</li><li>Utilize and support electronic document management systems.</li><li>Provide mentorship for entry-level regulatory associates.</li><li>Understand and identify potential regulatory risks and recommend strategies based on current FDA/health authority requirements.</li><li>Manage multiple priorities and critically review documentation for regulatory submissions, providing input for necessary revisions.</li></ul>Essential Skills<ul><li>Experience with regulatory affairs, regulatory submissions, and regulatory documents.</li><li>Familiarity with FDA regulations and pharmaceutical industry standards.</li><li>Competence in CMC (Chemistry, Manufacturing, and Controls) processes.</li><li>Ability to author, organize, and prepare electronic (eCTD) regulatory filings.</li><li>Capability to understand and interpret FDA guidance and quality systems.</li></ul>Additional Skills &amp; Qualifications<ul><li>A minimum of 3 years experience supporting filings within regulatory, preferably in the pharmaceutical industry.</li><li>Experience with any change control software.</li><li>Strong analytical and strategic thinking skills.</li></ul>Work EnvironmentThe position is based in a standard office environment, requiring a willingness to work in a team-based setting. Flexibility to work outside regular hours is required.Job Type &amp; LocationThis is a Contract position based out of St. Louis, MO.Pay and BenefitsThe pay range for this position is $32.00 - $37.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

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

Regulatory Affairs Specialist

Job Title: Regulatory Affairs SpecialistJob DescriptionThe Regulatory Affairs Specialist plays a crucial role in supporting US FDA applications (NDAs, ANDAs, DMFs) and international drug product applications. This position involves planning, authoring, compiling, and submitting statutory reports in eCTD format for marketed products according to FDA requirements. The role also includes reviewing and assessing CMC regulatory impacts of post-approval changes and providing regulatory strategies.Responsibilities<ul><li>Plan, author, compile, and submit statutory reports in eCTD format for marketed products per FDA requirements.</li><li>Review and assess CMC regulatory impact of post-approval changes proposed at the manufacturing site and provide regulatory strategy.</li><li>Plan, author, compile, submit, and manage variations and supplements for marketed products within and outside the United States.</li><li>Participate in cross-functional teams and provide health authority requirements needed for support of post-approval changes.</li><li>Author and review updates to marketed product labeling.</li><li>Maintain regulatory knowledge of current guidelines and regulations.</li><li>Maintain current regulatory databases and produce various reports as needed.</li><li>Utilize and support electronic document management systems.</li><li>Provide mentorship for entry-level regulatory associates.</li><li>Understand and identify potential regulatory risks and recommend strategies based on current FDA/health authority requirements.</li><li>Manage multiple priorities and critically review documentation for regulatory submissions, providing input for necessary revisions.</li></ul>Essential Skills<ul><li>Experience with regulatory affairs, regulatory submissions, and regulatory documents.</li><li>Familiarity with FDA regulations and pharmaceutical industry standards.</li><li>Competence in CMC (Chemistry, Manufacturing, and Controls) processes.</li><li>Ability to author, organize, and prepare electronic (eCTD) regulatory filings.</li><li>Capability to understand and interpret FDA guidance and quality systems.</li></ul>Additional Skills &amp; Qualifications<ul><li>A minimum of 3 years experience supporting filings within regulatory, preferably in the pharmaceutical industry.</li><li>Experience with any change control software.</li><li>Strong analytical and strategic thinking skills.</li></ul>Work EnvironmentThe position is based in a standard office environment, requiring a willingness to work in a team-based setting. Flexibility to work outside regular hours is required.Job Type &amp; LocationThis is a Contract position based out of St. Louis, MO.Pay and BenefitsThe pay range for this position is $32.00 - $37.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in St. Louis,MO.Application DeadlineThis position is anticipated to close on Feb 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: Regulatory AssistantJob DescriptionWe are seeking a dedicated and detail-oriented Regulatory Assistant to ensure that new and generic pharmaceutical products comply with established state and federal regulations. The role involves providing guidance for the submission of federal regulations, reviewing product labels and raw material information, and preparing electronic regulatory documents for submission to the FDA.Responsibilities<ul><li>Ensure compliance of pharmaceutical products with state and federal regulations.</li><li>Provide guidance for the submission of federal regulatory documents.</li><li>Review and analyze product labels and raw material information.</li><li>Research and analyze industry-specific regulations in pharmaceutical manufacturing.</li><li>Prepare electronic regulatory documents for FDA review and submission.</li></ul>Essential Skills<ul><li>Experience in regulatory affairs and documentation.</li><li>Bachelor's degree in Science.</li><li>Experience with regulatory labeling in a regulated industry with FDA requirements.</li><li>Strong attention to detail.</li><li>Proficiency in Microsoft Office.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience in documentation or regulatory affairs is preferred.</li><li>Experience in a regulated industry such as cosmetics or food is a plus.</li></ul>Work EnvironmentThe position is located in a building adjacent to the main administration and regulatory affairs office. The team is smaller, and the role may require working independently at times. The position follows a first shift schedule from Monday to Friday, 8 AM to 5 PM.Job Type &amp; LocationThis is a Contract to Hire position based out of Columbus, OH.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 Columbus,OH.Application DeadlineThis position is anticipated to close on Feb 27, 2026.<h2>About Actalent</h2>

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

Regulatory Assistant

We are hiring for a Regulatory Affairs Technician role that will be focused on reviewing regulatory documentation to be submitted to the FDA and other regulatory bodies for review. This role is primarily a desk based job and will specifically focus on working with regulatory requirements around labeling pharmaceutical products. An ideal candidate for this role will have a Bachelors Degree in a Scientific field. This is an entry-level position and a great opportunity for someone who wants to be in the sciences without being in a laboratory environment.Job DescriptionWe are seeking a dedicated and detail-oriented Regulatory Affairs Technician to ensure that new and generic pharmaceutical products comply with established state and federal regulations. The role involves providing guidance for the submission of federal regulations, reviewing product labels and raw material information, and preparing electronic regulatory documents for submission to the FDA.Responsibilities<ul><li>Ensure compliance of pharmaceutical products with state and federal regulations.</li><li>Provide guidance for the submission of federal regulatory documents.</li><li>Review and analyze product labels and raw material information.</li><li>Research and analyze industry-specific regulations in pharmaceutical manufacturing.</li><li>Prepare electronic regulatory documents for FDA review and submission.</li></ul>Qualifications:<ul><li>Bachelor's degree in a scientific field.</li><li>Comfortability with being in a desk based, non-laboratory role in the sciences.</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Columbus, OH.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 Columbus,OH.Application DeadlineThis position is anticipated to close on Feb 27, 2026.<h2>About Actalent</h2>

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

Regulatory Compliance EngineerResponsibilities<ul><li>Plan and execute transmitter compliance testing, including output power, bandwidth, frequency stability, and emissions.</li><li>Own and manage Part 15 unintentional radiator testing for radiated and conducted emissions.</li><li>Coordinate compliance activities with external test labs and Telecom Certification Bodies (TCBs).</li><li>Support and manage MIL-STD environmental testing, including shock, vibration, temperature cycling, humidity, and altitude.</li><li>Lead debug and root cause analysis for test failures and performance margin issues.</li><li>Drive corrective actions such as shielding, grounding, filtering, layout improvements, and firmware changes.</li><li>Produce compliance documentation, including test plans, results summaries, FCC exhibits, and reports.</li><li>Work cross-functionally to ensure compliance is integrated into product design from the start.</li></ul>Essential Skills<ul><li>Bachelor’s or Associate degree in Electrical Engineering, Electronics, Systems Engineering, or a related field.</li><li>3+ years of experience in regulatory compliance or qualification testing for RF/electronic products.</li><li>Experience with FCC intentional radiator certification</li><li>Hands-on lab experience and strong debugging skills.</li><li>Proficiency in using RF/EMC instrumentation such as spectrum analyzers, RF power meters, signal generators, and antennas.</li><li>Experience with environmental qualification testing, such as MIL-STD-810 or equivalent.</li><li>Experience working directly with certification labs and regulatory agencies.</li><li>Strong understanding of RF design and EMI mitigation best practices.</li></ul>Additional Skills &amp; Qualifications<ul><li>Aerospace &amp; Defense industry experience.</li><li>Strong knowledge of EMI troubleshooting, grounding/shielding, filtering, and system-level mitigation.</li><li>Experience in test planning, documentation, and compliance report generation.</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Schaumburg, IL.Pay and BenefitsThe pay range for this position is $35.00 - $40.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Schaumburg,IL.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.

Regulatory Compliance Engineer

Job Title: Regulatory Compliance EngineerResponsibilities<ul><li>Plan and execute transmitter compliance testing, including output power, bandwidth, frequency stability, and emissions.</li><li>Own and manage Part 15 unintentional radiator testing for radiated and conducted emissions.</li><li>Coordinate compliance activities with external test labs and Telecom Certification Bodies (TCBs).</li><li>Support and manage MIL-STD environmental testing, including shock, vibration, temperature cycling, humidity, and altitude.</li><li>Lead debug and root cause analysis for test failures and performance margin issues.</li><li>Drive corrective actions such as shielding, grounding, filtering, layout improvements, and firmware changes.</li><li>Produce compliance documentation, including test plans, results summaries, FCC exhibits, and reports.</li><li>Work cross-functionally to ensure compliance is integrated into product design from the start.</li></ul>Essential Skills<ul><li>Bachelor’s or Associate degree in Electrical Engineering, Electronics, Systems Engineering, or a related field.</li><li>3+ years of experience in regulatory compliance or qualification testing for RF/electronic products.</li><li>Experience with FCC intentional radiator certification</li><li>Hands-on lab experience and strong debugging skills.</li><li>Proficiency in using RF/EMC instrumentation such as spectrum analyzers, RF power meters, signal generators, and antennas.</li><li>Experience with environmental qualification testing, such as MIL-STD-810 or equivalent.</li><li>Experience working directly with certification labs and regulatory agencies.</li><li>Strong understanding of RF design and EMI mitigation best practices.</li></ul>Additional Skills &amp; Qualifications<ul><li>Aerospace &amp; Defense industry experience.</li><li>Strong knowledge of EMI troubleshooting, grounding/shielding, filtering, and system-level mitigation.</li><li>Experience in test planning, documentation, and compliance report generation.</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of South Barrington, IL.Pay and BenefitsThe pay range for this position is $35.00 - $40.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in South Barrington,IL.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.

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