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<h3>Job Description</h3>
Job Description
Background: Tri-K is one of leading suppliers of natural actives such as proteins, peptides and a comprehensive cosmetic ingredients portfolio to the personal care industry. It has an R&amp;D center with state-of-the-art equipment and testing facilities. To strengthen its innovation capabilities and improve customer connectivity, the R&amp;D organization focuses on developing new innovative ideas, products, and formulations with proven efficacy. This senior level R&amp;D position is part of the manufacturing organization based in Derry, NH

Summary: 
We are seeking a highly motivated and experienced protein chemist to join our team. The ideal candidate should have a PhD in protein chemistry, biochemistry, or a related field, or have at least 3 years of experience in protein synthesis, characterization, purification, and analysis.
Essential Duties and Responsibilities include the following. Other duties may be assigned. 
<ul>
<li>Develop and optimize protein and peptide purification protocols.</li>
<li>Characterize and analyze proteins and peptides using techniques such as HPLC, SDS-PAGE, and LC-MS</li>
<li>Perform chemical reactions to implement protein modification. </li>
<li>Conduct protein stability studies and develop formulations to improve protein stability.</li>
<li>Collaborate with other scientists to develop new protein-based cosmetic ingredients and products.</li>
<li>Maintain and troubleshoot laboratory equipment.</li>
<li>Write technical reports and present findings to internal and external stakeholders.</li>
</ul>
<ul>
<li>Search and evaluate published literature to understand hair and skin substrates, new protein technologies and new methodologies.</li>
</ul>
<ul>
<li>Research the latest market trends, customer needs, and competitor positioning.</li>
<li>Provide guidance to the Technical Services Team in addressing customer inquiries in a direct and succinct manner.</li>
<li>Collaborate with the Sales, Marketing and Business Managers, to ensure effective marketing claims, and to ensure continued positive client relationships and to build relationships with new clients.</li>
</ul>
<ul>
<li>Investigate possibilities and benefits of line extensions and functional blends surpassing industry standards. </li>
<li>Research the feasibility of combining proteins with other chemistries and technology promoting synergistic effects.</li>
<li>Research prior patents to allow for “freedom to operate”. </li>
</ul>
<ul>
<li>Explore new partnerships and collaborations with academia. </li>
</ul>
Required Skills and Competencies
Strong Technical Background in Protein/Peptide Chemistry is required. The incumbent must have a strong understanding of protein/peptide behavior to modify, identify and purify the active proteins/peptides from a complex natural source. He/She should be open to new challenges and be able to implement creative and innovative approaches. 
Competencies
To perform the job successfully, an individual should demonstrate the following competencies:
<ul>
<li>Strong knowledge of protein chemistry and biochemistry</li>
<li>Experience with protein purification techniques such as chromatography and ultrafiltration</li>
<li>Experience with protein analysis techniques such as HPLC, SDS-PAGE, and LC-MS</li>
<li>Strong problem-solving and analytical skills</li>
<li>Excellent communication and interpersonal skills</li>
<li>Ability to work independently and in a team environment.</li>
<li>Strong technical, and strategic acumen. </li>
<li>Exceptional verbal, written communication, and presentation skills</li>
<li>Comfort &amp; capability to work effectively in a collaborative cross-functional organization.</li>
<li>Analytical, and Problem-Solving skills to find effective solutions and overcome challenges. </li>
<li>Project Management - Develop project plans; Complete projects on time and budget. </li>
<li>Strong time management and prioritization skills. </li>
<li>Innovation - Develop and present innovative approaches and ideas. </li>
</ul>

Qualifications:
The requirements listed below are representative of the knowledge, skill, and/or ability required.
Education/Experience:
PhD in protein chemistry, biochemistry, or a related field. Or have at least 3 years of experience in protein synthesis, characterization, purification, and analysis.
Scientific Language Ability:
Ability to read, analyze, and interpret scientific periodicals, professional journals, technical procedures, or governmental regulations. Ability to write reports, business correspondence, and procedure manuals. Ability to effectively present information and respond to questions from groups of managers, clients, and customers.
Analytical skills: 
Ability to solve practical problems and deal with numerous assumptions and variables in situations where only limited standardization exists. Knowledge of MS Suite and other PC tools is essential.
Physical Demands:
This position requires working at the Derry, NH R&amp;D center 5 days a week, unless travelling to attend trade shows or visit other Tri-K sites. 
Travel Requirements:
10% travel including domestic/international with overnight stays to drive business development efforts.

Senior Protein Chemist

<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 Description
Part Time Shift: Weekends, rotating Hourly Pay Range: $25.00-$30.00 (Based on experience)
POSITION SUMMARY 
Performs lab testing and associated activities within the Microbiology section, including Serology, Virology and Parasitology.
Essential Position Duties 
<ul>
<li>Reviews the daily specimen management report.</li>
<li>Troubleshoots and maintains the LIS and instruments interface and software.</li>
<li>Performs Clostidium difficile assays.</li>
<li>Resolves client problems as needed.</li>
<li>Performs and records all quality assurances systems required to maintain precision and accuracy, including proficiency testing.</li>
<li>Performs other tasks and procedures in Microbiology as required which are commensurate with education, training and experience.</li>
<li>Assists in maintaining adequate inventory of supplies.</li>
<li>Record lot numbers and ensures compliance with State requirements for documentation of lot numbers with quality control and specimen records.</li>
<li>Performs all clerical functions associated with the department.</li>
<li>Reads bacterial and viral cultures. Performs biochemical identification procedures as necessary and record MIC results. </li>
<li>Follows all safety protocols as outlines in safety manual.</li>
<li>Identifies and pursues self improvement needs.</li>
<li>Seeks coaching/mentoring when appropriate.</li>
<li>Performs other duties as assigned</li>
</ul>
Compliance Responsibilities 
<ul>
<li>Participates in required orientation, Compliance and HIPAA training programs.</li>
<li>Cooperates with monitoring and audit functions and investigations.</li>
<li>Participates, as requested, in process improvement responsibilities.</li>
</ul>
POSITION QUALIFICATIONS 
Core Competencies/Skill Sets 
<ul>
<li>Excellent verbal and written communication skills.</li>
<li>Detail oriented and organizational skills.</li>
<li>Exercises accuracy and precision in completion of prescribed tasks and treatments.</li>
</ul>
Professional Experience/Educational Requirements 
<ul>
<li>Bachelor’s degree or MT (ASCP or equivalent preferred); Associates degree with MLT</li>
<li>Minimum of one (1) year experience in the area of Microbiology.</li>
<li>Some computer experience required.</li>
</ul>
Certification/Licensure
<ul>
<li>Must qualify as a clinical laboratory technologist under CLIA regulations.</li>
</ul>
Benefits:
TridentCare offers a competitive wage and robust benefit package to full time employees. Part time employees are eligible for many of the same below, pro-rated. Benefits include:
<ul>
<li>Two weeks of vacation time</li>
<li>Health Insurance after 30 days!</li>
<li>Sick time</li>
<li>8 paid holidays</li>
<li>Same day pay available</li>
<li>Medical insurance allowance, giving you the freedom to customize your plan to fit your needs</li>
<li>Dental insurance</li>
<li>Vision insurance</li>
<li>Disability insurance</li>
<li>Company paid life insurance</li>
<li>401(k)</li>
</ul>
#MBX

Microbiologist/ MLT, Microbiologist

<h3>Job Description</h3>
Job Description
Discover Veranova:
At Veranova, we believe people are our most important asset, and we are dedicated to building the most talented workforce in our industry. Our commitment to uncompromising focus on quality, compliance, safety, and excellence in delivery shapes everything we do. We are not just looking for skills; we are seeking innovative individuals who have a mindset open to learning and growth, and a desire to make a difference.
Veranova is a global leader in the development and manufacturing of complex active pharmaceutical ingredients (APIs) for pharma and biotech customers. With deep technical expertise and impressive flexibility, we develop solutions and processes that support and accelerate innovation. 
Join us on our mission to enable current and next-generation therapeutics to improve and save the lives of patients. 
Role Overview:
The Process R&amp;D Scientist plays a key role in developing and optimizing synthetic routes for complex active pharmaceutical ingredients (APIs). This position conducts small- to large-scale chemical reactions and generates high-quality data that supports project decision-making and innovation. Working under the guidance of technical leads, the role contributes to delivering projects on time, on spec, and within budget. It’s an excellent opportunity to deepen expertise while supporting impactful pharmaceutical development.
Core Responsibilities: 
<ul>
<li>Delivers experimental output with high scientific integrity, meeting targets, timelines, and quality expectations with guidance.</li>
<li>Exhibits strong safety awareness, conducts laboratory and operational activities safely, and maintains accountability for safe behavior in the work environment.</li>
<li>Maintains technical equipment and related services to ensure proper functionality.</li>
<li>Acts on feedback and demonstrates a continuous commitment to learning and professional development.</li>
<li>Leads technical and operational areas and supports troubleshooting for complex scientific issues with minimal guidance.</li>
<li>Shares knowledge, skills, and experience effectively with internal and external stakeholders; may lead focused projects as a key contact.</li>
<li>Keeps accurate, legible, and complete records of all experiments, observations, and equipment use.</li>
<li>Writes high-quality reports and delivers presentations to customers and management with some guidance, aligned with project milestones.</li>
<li>Contributes to maintaining strong customer relationships and identifies new commercial opportunities.</li>
<li>Actively supports the technical development of the department and the broader organization.</li>
<li>Ensures all documentation meets Veranova standards; supports audit readiness and participates in regulatory and customer audits as needed; reports near misses and safety incidents per company procedures; and ensures all work complies with applicable state and federal regulations, including GMP, DEA, and FDA requirements.</li>
<li>Adheres to all EHS policies and procedures; demonstrates strong technical and procedural proficiency in applying EHS standards; supports EHS audit readiness and participates in audits; reports and cooperates fully in investigations of near misses and incidents; and upholds Veranova’s EHS commitments by integrating ISO 14001, OHSAS 18001, and Sustainability 2025 principles into daily work.</li>
<li>Performs additional duties within the employee’s skills and abilities as reasonably assigned.</li>
</ul>
Qualifications: 
Required
<ul>
<li>PhD degree (or equivalent experience) in a chemistry related discipline.</li>
<li>Proficiency with relevant lab and analytical techniques.</li>
<li>Previous industry experience in relevant areas.</li>
<li>Proficiency with relevant analytical techniques within an industry environment.</li>
<li>Ability to write clear and concise technical reports.</li>
<li>Good understanding of Microsoft Office and other relevant technical software platforms.</li>
<li>Skilled in written and spoken communication and proven ability to effectively interact with management.</li>
<li>Demonstrates good judgment, quick decision-making skills, and the ability to work independently and in a team environment.</li>
</ul>
Special Factors 
<ul>
<li>Must be able to stand, walk, and manually operate objects, tools, or controls; reach with hands or arms; and climb, balance, stoop, kneel, or crouch when necessary for the job activity.</li>
<li>Must be able to lift and/or move up to 50 pounds.</li>
<li>Specific vision abilities include near, distance, peripheral, color perception, and the ability to adjust focus.</li>
<li>May regularly work with moving mechanical parts and may work with toxic or caustic chemicals.</li>
<li>May work in humid areas with low or high temperatures.</li>
<li>May be required to work with a respirator or operate with full-body Tyvek suits and supplied air or PAPR.</li>
</ul>
Salary Range: $105,000 - $120,000 annual base salary 
Our Commitment:
<ul>
<li>Health &amp; Wellness: Comprehensive health &amp; wellness benefits. Access to mental health resources and wellness programs. Generous PTO and holiday pay policies. </li>
<li>Financial Wellness: Veranova is committed to fair and transparent compensation practices. This includes a competitive base salary, eligibility for performance-based bonuses, and an attractive 401(k) Plan with company match. Salary ranges reflect the scope and expectations of the role, and are based on market data, internal equity, and role-specific factors. Final compensation may vary depending on experience, skills, education, and business needs.</li>
<li>Professional Development: Opportunities for continuous learning through LinkedIn Learning, workshops, conferences, and mentorship. Tuition Assistance for Undergraduate and Graduate degree programs.</li>
<li>Inclusive Culture: At Veranova, an inclusive culture is integral to our values. We welcome people with diverse experiences and perspectives who share our mission to improve and save lives. Even if you don’t meet every qualification, we encourage you to apply. Veterans, first responders, and those transitioning from military to civilian life bring valuable skills that strengthen our team.</li>
</ul>
Additional Information:
Applicants for this role must be authorized to work in the United States without further employer sponsorship. 
Agency and Search Firm Representatives: Veranova does not accept unsolicited resumes from agencies and/or search firms for this job posting. 
All your information will be kept confidential according to EEO guidelines.
Veranova is an Equal Opportunity Employer. It is the policy of Veranova to provide equal employment access and opportunity to all persons regardless of age, race, color, national origin, religion, sex, sexual orientation, gender identity and/or expression, physical or mental disability, genetic information, citizenship, marital status, veteran status, or any other characteristic protected by federal, state, or local law.
All applications are carefully considered, and your details will be stored on our secure Application Management System. This is used throughout Veranova for the selection of suitable candidates for our vacancies as they arise. Veranova respects your privacy and is committed to protecting your personal information. For more information about how your personal data is used please view our privacy notice.
#LI-Onsite

Scientist - Process Research & Development

<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 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 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 Title:Senior Scientist
Reports To: Operations Manager
Position Location: Franklin, MA 
FLSA Status (Exempt/Non-Exempt): Exempt 
Position Summary: 
Provides primary technical and scientific leadership for products manufactured and processed by the Franklin site. Interfaces with customers and Business Development team members to support Proficiency Testing Programs, Seroconversion Panels and special projects. Provides project management for new projects and improvement activities. Work closely with manufacturing supervisor and team to ensure all NatTrol and proficiency project timelines are achieved
Key Responsibilities: 
<ul>
<li>Manage existing Proficiency Testing Programs between Business Development and partners.</li>
<li>Coordinate with manufacturing supervisor to ensure all project timelines are on schedule.</li>
<li>Field questions and lead troubleshooting efforts around technical concerns regarding products produced at Franklin site. </li>
<li>Support the Business Development team with customer interactions on capabilities, requirements, and technical discussions.</li>
<li>Partner with the R&amp;D team to support special customer requests and projects. </li>
<li>Manage implementation of current and new project requirements at the Franklin site. </li>
<li>Support cost roll-up for special projects to allow for commercialization.</li>
<li>Maintain Proficiency Testing calendar based on customer requirements, develop production schedule, and track manufacturing events to ensure 100% adherence. </li>
<li>Expedite production through appropriate channels to avoid delays.</li>
<li>Act as program lead for new projects and Seroconversion Panel product lines. Maintain documentation, manage inventory levels, and provide technical leadership.</li>
<li>Coordinate customer testing and outside testing of materials as required by contract.</li>
<li>Review all customer specifications and timelines, ensuring the business’s ability to comply. Provide technical guidance to customer as needed to meet their requirements. </li>
<li>Author COAs based on customer specifications. </li>
<li>Review, revise, and approve manufacturing Standard Operating Procedures as needed.</li>
<li>Review and approve process and equipment validation protocols associated with manufacturing.</li>
<li>Perform other duties as assigned.</li>
</ul>
Education: 
<ul>
<li>Bachelor’s degree in Biochemistry or related field. MS degree, preferred.</li>
</ul>

Experience: 
<ul>
<li>5+ years of progressive related experience.</li>
</ul>
Minimum Requirements/Qualifications: 
<ul>
<li>Experience in biological production environments.</li>
<li>Solid understanding of GMP and ISO 13485 standards. </li>
<li>Demonstrated project management experience.</li>
<li>Excellent interpersonal communication skills with internal and external customers. </li>
<li>Thrives in a fast-paced, collaborative environment, efficiently works under pressure, within deadlines or other time essential constraints.</li>
<li>Excellent communication skills, both written and verbal, to clearly and concisely communicate to all levels of the organization</li>
<li>Strong work ethic and an ability to excel within a rapidly changing and growing organization.</li>
</ul>
Compensation &amp; Benefits:
<ul>
<li>Salary Range: $70,000-$100,000, depending on location, experience, and qualifications.</li>
<li>Benefits coverage begins day 1, including the following:</li>
<li>Medical, Dental, Vision Insurance</li>
<li>Disability Insurance </li>
<li>Life Insurance</li>
<li>401(k) company match</li>
<li>Paid Time Off (15 days annually)</li>
<li>Paid Holiday time (10 company-designated days)</li>
<li>Tuition Assistance </li>
<li>Additional benefits available with company package </li>
</ul>
This position has not been approved for Relocation Assistance.
The above statements are intended to describe the general nature and level of the work being performed by people assigned to this job. They are not an exhaustive list of all of the duties and responsibilities associated with it.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, protected veteran status, or disability status.

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