field_job_occupational_field_parents_all

field_job_employment_type

job_organization_name

city

state

<h3>Job Description</h3>
Job Description
Job Title: Senior Scientist
Job Description
We are seeking a highly skilled and motivated Senior Scientist to join our team. This role involves the start-up of a lab, including the setup of single-use technology bioreactors, ensuring all documentation meets compliance and validation standards. The successful candidate will manage materials and inventory, establish a structured storage area, and implement an efficient inventory management system. Additionally, you will support project and operational activities, assisting the project team in achieving daily and weekly milestones and facilitating lab equipment testing and setup.
Responsibilities
<ul>
<li>Setup single-use technology bioreactors, including equipment delivery, unboxing, assembly, setup, and operation.</li>
<li>Troubleshoot issues and ensure documentation meets compliance and validation standards.</li>
<li>Establish and organize a structured storage area for raw materials and spare equipment.</li>
<li>Implement an inventory management system to track consumables, reagents, and spare parts.</li>
<li>Support the overall project team in meeting key daily and weekly milestones.</li>
<li>Facilitate receipt, setup, and functional testing of lab equipment at all scales.</li>
<li>Develop and maintain a list of spares for all deployed equipment.</li>
</ul>
Essential Skills
<ul>
<li>Experienced with single-use technology bioreactors: unbox, setup, start-up, troubleshoot, and operate.</li>
<li>Understanding of turnover packages (TOPs).</li>
<li>Proficiency with DeltaV distributed control system.</li>
<li>Bachelor’s degree in Biotechnology, Biochemistry, Chemical Engineering, or a related field.</li>
<li>Minimum 5 years of experience in lab operations or bioprocessing involving single-use technologies.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Proven ability to work cross-functionally with engineering, procurement, and project management teams.</li>
<li>Comfortable working with a remote manager and providing weekly updates.</li>
<li>Willingness to track work completed on a weekly basis and monitor deliverables.</li>
<li>Ability to organize schedule and work independently.</li>
</ul>
Work Environment
This role is based in a lab environment onsite, requiring hands-on work with advanced technologies and equipment. The successful candidate will be comfortable working independently and collaboratively, with a focus on achieving project milestones and maintaining an organized workspace.
Job Type &amp; Location
This is a Contract position based out of Plainville, MA.
Pay and Benefits
The pay range for this position is $57.00 - $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 Type
This is a fully onsite position in Plainville,MA.
Application Deadline
This position is anticipated to close on Dec 15, 2025.
About Actalent
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 <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

Senior Scientist

<h3>Job Description</h3>
Job DescriptionSalary: 
JOB SUMMARY
The Microbiologist conducts validation and feasibility testing for quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products through compendial methods and client specific test protocols.
 
PRIMARY DUTIES AND RESPONSIBILITIES
<ul>
<li>Performs validation testing to analyze samples to determine an accurate microbiological procedure for the following analyses: Microbial enumeration methods, absence of specified microorganisms, endotoxin, and water quality analysis (bioburden, TOC, Conductivity).</li>
<li>Performs Disinfectant Efficacy testing for clients facilities utilizing specific disinfectants, surfaces, and organisms determined by the clients.</li>
<li>Perform feasibility work with guidance from USP and BA SOPs. Being able to work independently with little to no guidance to figure out and apply test methods to different products and materials.</li>
<li>Documents work in a clear and organized manner.</li>
<li>Revises procedures and ELNs under close supervision.</li>
<li>Writes validation reports and client protocols for QC Micro to follow for routine testing.</li>
<li>Follows all safety rules and regulations and conducts periodic safety audits.</li>
<li>Follows all cGMP rules and regulations.</li>
<li>Under close supervision confers with Microbiologists and other client personnel regarding research, procedures performed, related results and prepares reports.</li>
<li>Under close supervision will be trained to become proficient at assigned tasks in order to become subject matter experts.</li>
<li>Performs data generation and problem solving with a minimal rework.</li>
<li>Works under close supervision to ensure all work performed is executed in compliance with standard operating procedures, good manufacturing practices, and the regulations of the Food and Drug Administration.</li>
<li>Ensures all work performed strictly adheres to Company, client and Pharmacopeial methodologies.</li>
<li>Performs system maintenance and calibrations to ensure equipment is operating with specified requirements.</li>
<li>Proper handling of hazardous waste in compliance with the Company and DES hazardous waste rules.</li>
</ul>
REQUIREMENTS &amp; QUALIFICATIONS
Qualifications include a BA or BS degree in Microbiology or related science discipline with 0-2 years of related experience is required. Knowledge of cGMP and related compliance regulations and guidances is preferred.
 
MINIMUM SKILLS REQUIREMENTS
<ul>
<li>Must have the ability and skill to perform the detailed job requirements noted above competently, safely and proficiently.</li>
<li>A self-starter, motivated person who possesses good interpersonal skills capable of effectively interacting with all departments and client personnel.</li>
<li>Must have excellent organizational, verbal communication and technical documentation skills.</li>
<li>Solid computer skills.</li>
<li>Knowledge of safe laboratory practices, including the proper procedures in handling chemicals and samples.</li>
<li>Must be a team player with integrity and concern for the quality of Company products, services and staff members.</li>
</ul>

Microbiologist I, VD

<h3>Job Description</h3>
Job DescriptionCompany Description 
The work we do at Eurofins Professional Scientific Services matters, and so do our employees. At Eurofins PSS, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package.
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.
If you’re looking for a rewarding career, a place to call home, apply with us today.
Job Description 
We are seeking a highly skilled, passionate, and motivated scientist to join our diabetes team. This position will play a key lab-based role in advancing iPSC stem cell engineering and will contribute to the development of the next generation of islet cell therapies. Successful candidates will have experience with gene editing, molecular biology techniques, assay development, and human iPSC cell culture, differentiation, and banking.
Key Responsibilities:
<ul>
<li>Enabling and advancing iPSC gene editing, cell line development, and evaluation of differentiated cells.</li>
<li>Routine iPSC cell culture, passaging, and media making.</li>
<li>Optimize workflows for iPSC CRISPR based gene-editing, gRNA screening, and delivery.</li>
<li>Optimize and perform assays for on-/off-target analysis via PCR and NGS workflows.</li>
<li>Generate clonal gene edited iPSC lines and characterize via flow cytometry, ddPCR, dPCR and qPCR.</li>
<li>Culture and execute routine directed differentiation of human iPSCs to pancreatic islets performing drug substance assessments such as cell counts, viability, and metabolite assessments.</li>
<li>Assist scientists in the team to evaluate and design mitigation strategies to ensure genomic stability of the iPSC lines and drug substance.</li>
<li>Collaborate cross-functionally to support transfer of R&amp;D assays to GMP.</li>
<li>Maintain accurate and detailed records of all experiments, synthesize results, prepare reports, and present in meetings. Contribute to SOP development.</li>
<li>Work seamlessly in executing workplans and meeting deadlines.</li>
</ul>
Qualifications 
Minimum Required Qualifications:
<ul>
<li>B.S. in Stem Cell Biology, Cell Biology, Bioengineering or a related field with 3-4 years relevant industry experience in gene editing and cell therapy.&nbsp; M.S. in Stem Cell Biology, Cell Biology, Bioengineering or related field with 1-2 years relevant industry experience in gene editing and cell therapy.</li>
<li>Extensive hands-on experience with human iPSC culture, gene editing, and molecular biology techniques.</li>
<li>Proficiency in CRISPR gene editing and cell line development, including optimization of protocols, familiarity with flow-based sorting.</li>
<li>Proficiency in molecular biology techniques including construct design, PCR, ddPCR, dPCR, and NGS.</li>
<li>Hands-on experience with assay development including luciferase assays, ELISA, and flow cytometry.</li>
<li>Hands-on experience with cell delivery methods of gene editing tools.</li>
<li>Excellent communication and interpersonal skills, with the ability to work effectively in a team-oriented environment.</li>
<li>Strong organizational skills and diligent record keeping.</li>
</ul>
Preferred Qualifications:
<ul>
<li>Hands-on experience in pancreatic islet directed differentiation.</li>
<li>Hands-on experience in transitioning research-grade processes to GMP-grade.</li>
<li>Familiarity with electronic lab notebook (ELN) documentation.</li>
<li>Authorization to work in the United States indefinitely without restriction or sponsorship.</li>
</ul>
 Additional Information 
Position is Full Time, Monday-Friday, 8am-5pm with occasional weekends (on a rotational basis to support cell culture). Candidates currently living within a commutable distance of Boston, MA are encouraged to apply.
What to Expect in the Hiring Process: 
<ul>
<li>10-15 Minute Phone Interview with Region Recruiter</li>
<li>45-60 Minute Virtual Interview with Manager and/or Group Leader</li>
<li>45-60 Minute In-Person Meeting over Coffee for a Casual Discussion of the Role</li>
</ul>
What We Offer:
<ul>
<li>Target pay range: $37-41/hr</li>
<li>Excellent full-time benefits including comprehensive medical coverage, dental, and vision options</li>
<li>Life and disability insurance</li>
<li>401(k) with company match</li>
<li>Paid vacation and holidays</li>
<li>Yearly goal-based bonus &amp; eligibility for merit-based increases</li>
</ul>
Eurofins Lancaster Laboratories Professional Scientific Services® (PSS) is a global, award-winning insourcing solution that places our people at our clients’ sites dedicated to running and managing laboratory services while eliminating headcount, co-employment, and project-management worries.
We infuse our 55-year track record of scientific and laboratory operations expertise, as well as HR, and a great place to work best practices, to recruit, hire, train, and manage highly qualified scientists to perform laboratory services using our client’s quality systems and equipment.
To learn more about Eurofins Lancaster Laboratories, please explore our website <a href="http://www.eurofinsus.com" target="_blank">www.eurofinsus.com</a>
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Associate Scientist, Gene Editing and iPSC Engineering

<h3>Job Description</h3>
Job Description Job Title: Bench Chemist
Location: Hadley, MA
Job Type: Contract-to-Hire
Schedule: Monday–Friday, 8:00 AM – 5:00 PM
About the Role
Are you passionate about chemistry and eager to make an impact in a dynamic laboratory setting? We’re looking for a Bench Chemist who thrives on precision, problem-solving, and innovation. In this role, you’ll work with cutting-edge instrumentation and collaborate with a team dedicated to delivering high-quality results that drive product excellence.
This is an exciting opportunity to join a growing organization where your expertise will directly contribute to advancing science and improving product quality.
What You’ll Do
<ul>
<li>Perform LC and GC testing on raw materials, in-process samples, and finished goods.</li>
<li>Prepare samples, run calibration curves, and ensure system suitability through integration reviews.</li>
<li>Execute wet chemistry techniques such as pH measurement, titrations, and loss on drying (LOD).</li>
<li>Conduct first-line instrument maintenance and troubleshooting to keep operations running smoothly.</li>
<li>Support method validation efforts focusing on accuracy, precision, and detection limits.</li>
<li>Maintain a clean, organized lab environment and assist with inventory management.</li>
<li>Draft and review SOPs to uphold compliance and quality standards.</li>
</ul>
What We’re Looking For
<ul>
<li>Education: Master’s degree in Chemistry or Analytical Chemistry with 3–5 years of QC lab experience (food or supplement industry preferred).</li>
<li>Technical Skills: Proficient in HPLC and GC systems, chromatography software (OpenLab, ChemStation), and wet chemistry techniques.</li>
<li>Knowledge: Familiarity with USP/AOAC methods and cGMP documentation.</li>
<li>Strong commitment to lab safety, accuracy, and continuous improvement.</li>
</ul>
Preferred:
<ul>
<li>Bachelor’s degree in Chemistry with equivalent experience.</li>
<li>Background in organic chemistry, formulation, or R&amp;D.</li>
</ul>
Why Join Us?
<ul>
<li>Work with state-of-the-art equipment in a collaborative, science-driven environment.</li>
<li>Opportunity for career growth through a contract-to-hire pathway.</li>
<li>Be part of a team that values innovation, quality, and professional development.</li>
</ul>
Job Type &amp; Location
This is a Contract to Hire position based out of Hadley, MA.
Pay and Benefits
The pay range for this position is $40.00 - $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 Type
This is a fully onsite position in Hadley,MA.
Application Deadline
This position is anticipated to close on Dec 12, 2025.
About Actalent
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 <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

Bench Chemist

<h3>Job Description</h3>
Job Description
Description
As a Microbiologist, you will conduct general food microbiological testing, including pathogenic microorganism analysis, under the guidance of the Quality Assurance Supervisor or as outlined in the protocol. You will obtain samples from production, process sample preparations for micro testing, including media preparation as directed, and count and record micro plate counts. Additionally, you will assist in processing samples from receipt through testing, ensuring thorough documentation and recordkeeping, including data entry in the internal electronic system, and communicate promptly with the Quality Assurance Supervisor.
 - Conduct general food micro testing, including generic pathogenic micro testing.
 - Obtain and process samples for micro testing, including media preparation.
 - Count and record micro plate counts.
 - Conduct specific micro testing under the guidance of the microbiologist.
 - Assist in processing samples from receipt through testing, including documentation and recordkeeping.
 - Communicate promptly with the Quality Assurance Supervisor.
 Record SOP.
 - Adhere to good manufacturing practices (GMP) and good laboratory practices (GLP) at all times.
 - Proficiency in microbiology and environmental monitoring.
 - Expertise in aseptic techniques and microbiology testing.
 - Experience with sample preparation and media preparation.
 - Knowledge in bioburden testing and food science.
 - Experience in food analysis testing.
Additional Skills &amp; Qualifications
• 1 -2 years micro test or food analysis lab experiences and basic knowledge of microbiology 
• Prior QA/QC experience in food manufacturing is a plus
• B.S. degree in food, chemistry, microbiology, biology or related is required
Experience Level
Entry Level
Job Type &amp; Location
This is a Contract to Hire position based out of Ayer, MA.
Pay and Benefits
The pay range for this position is $26.00 - $26.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
 • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Ayer,MA.
Application Deadline
This position is anticipated to close on Dec 11, 2025.
About Actalent
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 <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

Microbiologist

<h3>Job Description</h3>
Job DescriptionThis role will lead the development and improvement of nutritional beverages and powders from concept to commercialization, driving innovation that ensures exceptional quality, stability, and clinical impact.ResponsibilitiesDevelop and optimize nutritional beverage and powder formulations that meet nutritional, sensory, and stability goals. Partner with Medical Nutrition, Marketing, and Sales to align product design with business and patient needs. Research and evaluate new ingredients and explore new medical nutrition opportunities. Support leadership with technical and scientific expertise for product and clinical development. Build vendor relationships to source ingredients that meet product requirements. Present company research at scientific meetings and conferences. Ensure strong intellectual property protection for new products and processes. Follow all GMP, food safety, and workplace safety policies. BenefitsCompetitive salary and performance-based bonus (12.5%) program Comprehensive health, dental, and vision insurance Paid time off and holidays 401(k) with company match Opportunities for professional growth and advancement Employee discount programs

Senior Food Scientist (beverage, supplement, nutraceutical, or biotech industry)

<h3>Job Description</h3>
Job Description
Job Description
We are seeking a highly skilled and motivated Sr Scientist to join our team. This role involves the start-up of a lab, including the setup of single-use technology bioreactors, ensuring all documentation meets compliance and validation standards. The successful candidate will manage materials and inventory, establish a structured storage area, and implement an efficient inventory management system. Additionally, you will support project and operational activities, assisting the project team in achieving daily and weekly milestones and facilitating lab equipment testing and setup.
Responsibilities
<ul>
<li>Setup single-use technology bioreactors, including equipment delivery, unboxing, assembly, setup, and operation.</li>
<li>Troubleshoot issues and ensure documentation meets compliance and validation standards.</li>
<li>Establish and organize a structured storage area for raw materials and spare equipment.</li>
<li>Implement an inventory management system to track consumables, reagents, and spare parts.</li>
<li>Support the overall project team in meeting key daily and weekly milestones.</li>
<li>Facilitate receipt, setup, and functional testing of lab equipment at all scales.</li>
<li>Develop and maintain a list of spares for all deployed equipment.</li>
</ul>
Essential Skills
<ul>
<li>Experienced with single-use technology bioreactors: unbox, setup, start-up, troubleshoot, and operate.</li>
<li>Understanding of turnover packages (TOPs).</li>
<li>Proficiency with DeltaV distributed control system.</li>
<li>Bachelor’s degree in Biotechnology, Biochemistry, Chemical Engineering, or a related field.</li>
<li>Minimum 5 years of experience in lab operations or bioprocessing involving single-use technologies.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Proven ability to work cross-functionally with engineering, procurement, and project management teams.</li>
<li>Comfortable working with a remote manager and providing weekly updates.</li>
<li>Willingness to track work completed on a weekly basis and monitor deliverables.</li>
<li>Ability to organize schedule and work independently.</li>
</ul>
Work Environment
This role is based in a lab environment onsite, requiring hands-on work with advanced technologies and equipment. The successful candidate will be comfortable working independently and collaboratively, with a focus on achieving project milestones and maintaining an organized workspace.
Job Type &amp; Location
This is a Contract position based out of Plainville, MA.
Pay and Benefits
The pay range for this position is $57.00 - $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 Type
This is a fully onsite position in Plainville,MA.
Application Deadline
This position is anticipated to close on Dec 12, 2025.
About Actalent
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 <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

<h3>Job Description</h3>
Job DescriptionQC Chemist II &amp; III – Pharmaceutical Manufacturing (Relocation Offered!)
Ready to take your analytical skills to the next level? Join a leading pharmaceutical team where precision, innovation, and quality drive everything we do. We’re hiring QC Chemists (Levels II &amp; III) to perform critical testing and ensure compliance in a dynamic cGMP environment.
What You’ll Do:
<ul>
<li>Perform routine and advanced testing using cutting-edge instruments such as HPLC, GC, ICP, Karl Fischer, and Particle Size Analyzers.</li>
<li>Conduct raw material testing and release activities to maintain product integrity.</li>
<li>Lead investigations and troubleshoot complex analytical challenges.</li>
<li>Operate specialized equipment and perform critical testing to support manufacturing and quality goals.</li>
<li>Ensure strict compliance with cGMP, data integrity, and good documentation practices.</li>
<li>Collaborate with cross-functional teams and contribute to continuous improvement initiatives.</li>
</ul>
What We’re Looking For:
<ul>
<li>Bachelor’s degree in Physical Sciences (Chemistry preferred); Master’s degree is a plus.</li>
<li>QC Chemist II: 2–3 years of industry experience (Co-op experience in cGMP setting considered).</li>
<li>QC Chemist III: 3–5+ years of industry experience.</li>
<li>Strong knowledge of analytical chemistry techniques and instrumentation.</li>
<li>Excellent organizational skills and ability to analyze complex data sets.</li>
<li>Proficiency in English (written and verbal) and Microsoft Office tools.</li>
</ul>
Why Join Us?
<ul>
<li>Competitive salary:
<ul>
<li>Level II: $75,000–$82,500</li>
<li>Level III: $83,000–$90,000</li>
</ul>
</li>
<li>Relocation assistance available – we’ll help you make the move!</li>
<li>Work in a state-of-the-art cGMP pharmaceutical environment.</li>
<li>Opportunity for career growth and skill development in a collaborative team setting.</li>
<li>General shift: Monday–Friday, 8:30 AM – 5:00 PM.</li>
</ul>
If you’re ready to advance your career and contribute to life-changing therapies, apply today and be part of something impactful!
Job Type &amp; Location
This is a Permanent position based out of Fall River, MA.
Pay and Benefits
The pay range for this position is $65000.00 - $90000.00/yr.
Health Vision Dental 401K
Workplace Type
This is a fully onsite position in Fall River,MA.
Application Deadline
This position is anticipated to close on Dec 12, 2025.
About Actalent
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 <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

849 Science Jobs