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<h3>Job Description</h3>
Job Description
We are seeking a Scientist to join our client’s Manufacturing Sciences &amp; Technology team in Devens, MA. This role supports the Materials and Cryogenics Science group in the life cycle management of raw materials, consumables, and single-use systems used in biopharmaceutical commercial manufacturing.
You will collaborate closely with Manufacturing, Quality Assurance, Quality Control, Supply Chain, and Procurement on cross-functional teams to ensure GMP compliance and continuity of supply.
Key responsibilities include:
<ul>
<li> Qualify alternative raw material suppliers and partner with Procurement to identify new options. </li>
<li> Recommend and lead necessary testing to qualify materials for GMP manufacturing. </li>
<li> Author technical equivalency assessments, specification comparisons, material characterization reports, and change controls. </li>
<li> Support material and consumable manufacturing investigations. </li>
<li> Manage supplier change notifications and evaluate risks to maintain GMP compliance. </li>
<li> Contribute to risk assessments and material specification development. </li>
<li> Partner with cross-functional teams to deliver results in a fast-paced, matrixed environment.</li>
</ul>
Requirements
Bachelor’s or Master’s degree in Material Science Engineering, Chemistry, or related field with 2+ years of industry experience, or a PhD. 
 Strong technical writing skills and ability to author GMP documentation. 
 Experience in cross-matrix team environments and stakeholder collaboration. 
 Proven ability to manage multiple projects in a fast-paced setting. 
 Independent contributor with strong communication and interpersonal skills. 
 Experience with GMP change controls and investigations preferred. 
 Familiarity with analytical techniques (FTIR, SEM-EDS, etc.) and data trending/analysis a plus. 
 Awareness of cGMP regulations and compliance requirements.
Benefits
Competitive hourly rate: $67.20 – $75.20/hr (W-2 only, no C2C)
 Hybrid schedule (50% onsite Tue–Thu; full onsite during the first month) 
 12-month contract with possible extension 
 Health benefits, holiday pay, and 401(k) program 
 Paid time off (UTO) and professional development support 
 Employee referral bonus program 
 Opportunity to contribute to high-impact projects with a leading biopharma company

Scientist - GMP Quality & Technical Writing (Hybrid, Devens MA)

<h3>Job Description</h3>
Job Description
Job Title:&nbsp;Analytical Chemist – Method Development &amp; Validation
Location:&nbsp;Tewkesbury, MA
Employment Type:&nbsp;Full Time - Permanent 
Experience Level:&nbsp;Intermediate
Overview:
We are seeking a highly skilled&nbsp;Analytical Chemist&nbsp;to join our team in supporting the development, validation, and implementation of analytical methods for pharmaceutical products. This role involves hands-on testing using advanced instrumentation, troubleshooting analytical issues, and ensuring compliance with GMP standards. The ideal candidate will have a strong experience in analytical chemistry and experience with a wide range of techniques and equipment.
Key Responsibilities:
<ul>
<li>Develop and optimize new analytical methods and techniques for product release.</li>
<li>Validate and verify analytical methods in accordance with regulatory and internal standards.</li>
<li>Investigate out-of-specification (OOS) results, out-of-trend (OOT) data, and equipment failures.</li>
<li>Analyze and present trending data to support method development and validation efforts.</li>
<li>Perform analytical testing of organic and inorganic compounds using FTIR, HPLC, NMR, LCMS, GCMS, ICP-MS, GC, and wet chemistry techniques.</li>
<li>Author test procedures and provide analytical support for research and development projects.</li>
<li>Follow GMP guidelines and contribute to continuous improvement initiatives.</li>
<li>Train and mentor junior team members as needed.</li>
</ul>
Required Skills &amp; Expertise:
<ul>
<li>Strong proficiency in analytical techniques including NMR, GCMS, HPLC, FTIR, LCMS, ICP-MS, and wet chemistry.</li>
<li>Deep understanding of GMP regulations and quality systems.</li>
<li>Experience conducting method development, validation, and troubleshooting.</li>
<li>Ability to work independently and collaboratively in a fast-paced environment.</li>
</ul>
Qualifications:
<ul>
<li>Master’s degree (MS) in Chemistry or Biochemistry with 3–5 years of relevant experience, or</li>
<li>Bachelor’s degree (BS) in Chemistry or Biochemistry with 5–7 years of experience.</li>
<li>Proven experience working with advanced analytical instrumentation in a pharmaceutical setting.</li>
</ul>
If interested, please reach out directly to Lindsee Allienello at lallienello @ actalentservices.com. 
Pay and Benefits
The pay range for this position is $75000.00 - $85000.00/yr.
Company provides holiday, vacation, and 401k benefits. They will be able to gain bonuses past on company and personal performance.
Workplace Type
This is a fully onsite position in Tewksbury,MA.
Application Deadline
This position is anticipated to close on Sep 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.

Analytical Chemist

<h3>Job Description</h3>
Job DescriptionHiring for a Quality Control Lab Analyst in Hadley!
Job Description
We are seeking a dedicated Quality Control Lab Analyst to join our growing team. This role involves conducting GC testing of raw materials, in-process samples, and finished goods. The successful candidate will play a key role in ensuring the quality and safety of our products.
Responsibilities
<ul>
<li>Prepare samples across various matrices and run calibration curves and system suitability tests.</li>
<li>Perform wet chemistry tests, including pH, titrations, and loss on drying (LOD).</li>
<li>Provide first-line instrument care, such as column maintenance and addressing leaks and pump seals, following IQ/OQ/PQ guidelines.</li>
<li>Conduct basic troubleshooting and maintenance of laboratory instruments.</li>
<li>Support method validation work, focusing on accuracy, precision, LOD, and LOQ.</li>
<li>Flexibly support lab needs, including inventory management, lab cleanup, and notebook peer review.</li>
<li>Draft and review Standard Operating Procedures (SOPs).</li>
</ul>
Essential Skills
<ul>
<li>Bachelor's degree in Chemistry is necessary; a Master's degree in Chemistry or Analytical Chemistry is preferred.</li>
<li>3-5 years of experience in a QC lab within the food or supplement industry.</li>
<li>Demonstrated independent operation of HPLC and GC.</li>
<li>Experience with natural product or lipid-rich matrices, including small molecule testing like vitamins, fats, emulsifiers, and actives.</li>
<li>Working knowledge of USP/AOAC methods and cGMP documentation.</li>
<li>Proficiency in chromatography software such as OpenLab and ChemStation.</li>
<li>Strong lab safety mindset and approach to work.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Experience as a bench lab analyst or chemist.</li>
<li>Proficiency in titration and wet chemistry.</li>
<li>Experience with ICP-MS.</li>
</ul>
Work Environment
The position is based in a laboratory/manufacturing setting. The work schedule is Monday through Friday, with working hours from 8:30 am to 4:30 pm or 9 am to 5 pm. As a smaller organization looking to expand, this role offers significant opportunities for growth and influence in the day-to-day operations of the lab.
Job Type &amp; Location
This is a Contract to Hire position based out of Hadley, Massachusetts.
Pay and Benefits
The pay range for this position is $30.00 - $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 Sep 19, 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.

Qc Lab Analyst

<h3>Job Description</h3>
Job DescriptionCompany Description 
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.
In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to over 47,000 staff across a network of more than 900 independent companies in over 50 countries and operating more than 800 laboratories. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products, as well as providing innovative clinical diagnostic testing services, as one of the leading global emerging players in specialised clinical diagnostics testing
If you’re looking for a rewarding career, apply with us today!&nbsp;&nbsp;
Job Description 
We are seeking a detail-oriented and motivated&nbsp;QC Microbiologist II to support microbiological testing and laboratory operations in a&nbsp;GMP-regulated environment. This role is critical to ensuring the quality and safety of pharmaceutical products through sterility, endotoxin, and bioburden testing, as well as general lab support and data review.
Key Responsibilities
<ul>
<li>Perform&nbsp;endotoxin and bioburden testing&nbsp;using standard microbiological methods (e.g., membrane filtration, LAL)</li>
<li>Conduct&nbsp;sterility testing&nbsp;and support microbial challenge recovery of drug substances and raw materials</li>
<li>Prepare microbial cultures for&nbsp;validation protocols,&nbsp;developmental studies, and&nbsp;growth promotion testing</li>
<li>Perform&nbsp;growth promotion,&nbsp;mold spore suspension, and&nbsp;water activity testing</li>
<li>Read and interpret microbial plates and document results accurately</li>
<li>Maintain lab cleanliness and organization, including&nbsp;cold room 5S, stocking supplies, and general housekeeping</li>
<li>Review and verify data for accuracy and compliance with cGMP standards</li>
<li>Utilize&nbsp;LIMS&nbsp;and&nbsp;electronic laboratory notebooks&nbsp;for data entry and tracking</li>
</ul>
Qualifications 
<ul>
<li>Bachelor’s degree in Microbiology, Biology, or a related scientific field</li>
<li>1–2 years of relevant experience in a&nbsp;Quality Control Microbiology&nbsp;or similar laboratory setting</li>
<li>Hands-on experience with:
<ul>
<li>Bioburden testing&nbsp;(membrane filtration)</li>
<li>Endotoxin testing&nbsp;(LAL)</li>
<li>Sterility testing&nbsp;(preferred)</li>
<li>Aseptic techniques and microbial culture preparation</li>
</ul>
</li>
<li>Familiarity with&nbsp;cGMP guidelines&nbsp;and regulatory compliance</li>
<li>Proficiency in&nbsp;Microsoft Word and Excel</li>
<li>Strong understanding of&nbsp;experimental design, data interpretation, and scientific methodology</li>
<li>Authorized to work in the United States without restriction or sponsorship</li>
</ul>
 Additional Information 
What to Expect in the Hiring Process:&nbsp;
<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 Onsite Meeting with the Team&nbsp;</li>
</ul>
Additional Details:&nbsp;
The position is full-time, first shift, Monday-Friday from 8 am-5 pm. Candidates must be flexible to adapt to schedule&nbsp;changes requiring shift changes and/or weekend work, and overtime may be required as needed.&nbsp;Candidates living within a commutable distance of Andover, MA,&nbsp;are encouraged to apply.&nbsp;&nbsp;
Benefits
<ul>
<li>Comprehensive&nbsp;medical, dental, and vision&nbsp;coverage</li>
<li>Life and disability insurance</li>
<li>401(k)&nbsp;with company match</li>
<li>Paid vacation and holidays</li>
<li>Annual goal-based bonus&nbsp;and&nbsp;merit-based increases</li>
<li>$27–$30/hour (based on education and experience)</li>
</ul>
Eurofins Lancaster Laboratories Professional Scientific Services®&nbsp;(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&nbsp;<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.

QC Microbiologist II

<h3>Job Description</h3>
Job DescriptionJob Title: Scientist IV Location: Cambridge, MA 02141 Duration: 12 Months+ (Possible Extension) Shift: Standard shift Pay Range: $100 - $111/ hr. on W2 Must have experience: 
<ul>
<li>PHD or Master’s degree Molecular Biology, Cellular Biology, Genomics, or a related field. </li>
<li>Minimum of 1+ years of dedicated single cell and Next gen sequencing experience with demonstrated expertise in transcriptomics and spatial biology. </li>
<li>scRNA-seq and snRNA-seq, Bulk RNA-seq, Next-Gen Sequencing (NGS) </li>
<li>Preferred qualifications: 3-5 years of related of dedicated single cell and Next gen sequencing experience with demonstrated expertise in transcriptomics and spatial biology. </li>
<li>scRNA-seq and snRNA-seq o Spatial transcriptomics platforms (e.g., 10x Genomics Visium and/or Xenium, NanoString GeoMx). </li>
<li>Spatial proteomics technologies (e.g., Akoya CODEX/Phenocycler-Fusion) </li>
<li>Proficiency in tissue handling, imaging, and histological techniques. </li>
<li>Familiarity with bioinformatics tools and pipelines for omics data analysis. </li>
<li>Fully onsite role</li>
<li>Position is 100% lab-based</li>
</ul>
 Job Description: 
<ul>
<li>We are looking for a highly motivated and innovative scientist to join the Target, Disease &amp; Systems Biology (TDSB) department at Client as a Scientist. In this role, you will collaborate with the Pre-clinical Omics research team to investigate disease biology, uncover Client pathways and mechanisms, and identify strategies to address unmet medical needs across a range of therapeutic areas.</li>
<li>This position offers the opportunity to apply cutting-edge molecular biology and spatial technologies to advance our therapeutic discovery efforts. The ideal candidate will bring strong technical expertise in bulk RNA-seq, single-cell/single-nucleus RNA-seq (sc/snRNA-seq), spatial transcriptomics, and spatial proteomics to support a broad Product of research initiatives.</li>
</ul>
<ul>
<li>We are seeking someone who can lead and execute scientific research, analyze and present complex data, and communicate effectively with both expert and non-expert audiences. Strong organizational skills—including meticulous record keeping, planning and scheduling, and maintaining laboratory equipment—are essential. The successful candidate will be curious, Product, and creative in exploring new scientific directions and proposing innovative experimental approaches.</li>
<li>At Client, we are an innovative global healthcare company driven by a singular purpose: to chase the miracles of science to improve people’s lives. We offer a dynamic environment where you can thrive professionally, build meaningful connections, and push the boundaries of scientific discovery. Ready to begin your journey?</li>
</ul>
 Responsibilities:
<ul>
<li>Experimental Design &amp; Execution
<ul>
<li>Design and perform experiments using bulk RNA-seq, single-cell/single-nucleus RNA-seq (sc/snRNA-seq), NGS and spatial assays (GeoMx, Visium, Xenium, Phenocycler-Fusion) on human and non-human biological samples.</li>
<li>Optimize and troubleshoot protocols for molecular and spatial assays.</li>
</ul>
</li>
<li>Data Analysis &amp; Interpretation
<ul>
<li>Collaborate with bioinformatics teams to analyze high-dimensional omics data.</li>
<li>Interpret results to guide therapeutic target identification and validation.</li>
</ul>
</li>
<li>Technology Development &amp; Innovation
<ul>
<li>Evaluate and implement emerging molecular biology and spatial technologies.</li>
<li>Contribute to the development of Client workflows and platforms.</li>
</ul>
</li>
<li>Cross-functional Collaboration
<ul>
<li>Work closely with scientists across biology, chemistry, and computational disciplines.</li>
<li>Present findings in internal meetings and contribute to strategic research discussions.</li>
</ul>
</li>
<li>Documentation &amp; Reporting
<ul>
<li>Maintain detailed experimental records.</li>
<li>Prepare technical reports and presentations</li>
</ul>
</li>
</ul>
 Qualifications: Master’s degree or Ph.D. in Molecular Biology, Cellular Biology, Genomics, or a related field. 3–5 years of relevant experience in academia or industry, with demonstrated expertise in transcriptomics and spatial biology. Required qualifications:
<ul>
<li>scRNA-seq and snRNA-seq</li>
<li>Bulk RNA-seq</li>
<li>Next-Gen Sequencing (NGS)</li>
</ul>
<ul>
<li>Preferred qualifications:</li>
<li>Spatial transcriptomics platforms (e.g., 10x Genomics Visium and/or Xenium, NanoString GeoMx).</li>
<li>Spatial proteomics technologies (e.g., Akoya CODEX/Phenocycler-Fusion)</li>
<li>Proficiency in tissue handling, imaging, and histological techniques.</li>
<li>Familiarity with bioinformatics tools and pipelines for omics data analysis.</li>
<li>Strong problem-solving skills and ability to work independently and collaboratively.</li>
<li>Excellent communication and organizational skills.</li>
</ul>
 #sczr2

Scientist IV

<h3>Job Description</h3>
Job Description
Nanopath is a well-funded Series A-stage company working to develop a first-in-class in vitro diagnostics platform to revolutionize the way we diagnose disease. Nanopath works to disrupt existing lengthy molecular testing methodologies by bringing them closer to the patient. We aim to improve the lives of patients, starting with women, using our purpose-built tool that provides actionable information within a single office visit.
The company is headquartered at The Engine, the premier tough technology incubator in the Kendall Square ecosystem. As a company, we are committed to health equity and the design of solutions for underserved populations and low-resource settings. Corporate sustainability – both environmental and social - is at the forefront of our decision making.
About the Role
<ul>
<li>Support and manage a variety of assay development tasks. We are happy to tailor key responsibilities to the candidate ranging from molecular biology, cell culture, biomanufacturing, and bioinformatics. </li>
<li>Participate in critical team discussions, meetings, and presentations. Our co-ops are given critical and important projects!</li>
<li>Work directly with our tight-knit team of scientists and engineers to drive our product forward.</li>
<li>Learn more about cutting edge biophysics and interdisciplinary medtech development.</li>
</ul>
Qualifications:
<ul>
<li>Ability to commit to 15+ weeks of full-time and onsite work in Cambridge, MA</li>
<li>Sophomore or above with demonstrated experience through past internships or research projects</li>
<li>Excellent communication and presentation skills, highly organized with demonstrated curiosity, scientific rigor and creative problem-solving</li>
<li>Proactive self-starter with eagerness to adapt to a fast-paced, dynamic startup environment</li>
<li>Passion for technology translation and willingness to shape Nanopath's future</li>
<li>Current enrollment in a relevant academic program - we are open to undergraduate and graduate degree opportunities</li>
</ul>
This is a full-time onsite role in Cambridge, MA starting in early January, lasting no less than 5 months.
Don't meet every single requirement? Studies have shown that women and people of color are less likely to apply to jobs unless they meet every single qualification. At Nanopath we are dedicated to building a diverse and inclusive workplace, so if you're excited about this role but your past experience doesn't align perfectly with every point in the job description, we encourage you to apply anyways. You may be just the right candidate for this or other roles!
Nanopath Inc. is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.
Nanopath does not accept unsolicited resumes from recruiters or agencies and we will not be responsible for any fees related to resumes that are unsolicited. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of Nanopath, and Nanopath will not owe any referral or other fees with respect thereto.

Research Associate Co-op (January '26 Start)

<h3>Job Description</h3>
Chief Scientific Officer - Confidential Client (Biotechnology, Boston, MA) 
About the Company Our client is a cutting-edge biotechnology company dedicated to developing next-generation gene editing and gene therapy solutions for serious diseases. With a proprietary platform and strong financial backing, they are advancing multiple programs in CNS and neuromuscular disorders with the mission of delivering functional cures.
The Role The Chief Scientific Officer will serve as the scientific and strategic leader, driving discovery, translational, and preclinical efforts across the company's therapeutic portfolio. This executive will play a pivotal role in shaping the company's scientific vision and advancing novel programs toward clinical development.
Key Responsibilities
<ul>
<li>
Provide overall scientific and R&amp;D leadership across CNS and neuromuscular disease programs.
</li>
<li>
Lead teams spanning discovery, translational biology, and preclinical development.
</li>
<li>
Develop and execute strategies to progress gene editing/gene therapy programs from target validation to IND/CTA.
</li>
<li>
Partner with executive leadership, investors, and external collaborators to align R&amp;D with corporate strategy.
</li>
<li>
Stay at the forefront of advances in CNS, neuromuscular, and gene editing/therapy fields to maintain the company's leadership position.
</li>
</ul>
Qualifications
<ul>
<li>
PhD or MD/PhD in neuroscience, genetics, molecular biology, or related discipline.
</li>
<li>
10+ years of leadership experience in biotechnology or pharmaceutical R&amp;D.
</li>
<li>
Deep expertise in CNS or neuromuscular disorders and gene editing/therapy modalities (AAV, LNP, base or prime editing, etc.).
</li>
<li>
Demonstrated track record progressing programs through IND/CTA and into early clinical development.
</li>
<li>
Strong leadership, communication, and collaborative skills with the ability to inspire teams and engage stakeholders.
</li>
</ul>
Why Join? This is a rare opportunity to lead the scientific direction of a company at the forefront of gene editing, backed by a proprietary platform and committed to transforming patient outcomes in areas of urgent need.

Chief Scientific Officer - Gene Editing

<h3>Job Description</h3>
Job Description
Description
Support development and research of new methods and analytical techniques to be used to release new and existing products 
Validation and verification of analytical methods
perform investigations of out of specification, out of trends, equipment failure, etc. 
Present trending data to support development and validation following GMP guidelines
Perform analytical testing for organic and inorganic chemicals by using FTIR, HPLC, NMR LCMS, GCMS, ICP- MS, GC and wet chemistry
Create test procedures and provide analytical support for certain research products
Top Skills Details
NMR,GCMS,Hplc,FTIR,wet chemistry,analytical chemistry,LCMS
Additional Skills &amp; Qualifications
MS in chemistry or biochemistry with 3-5 years experience or a BS with 5-7 years experience
Experience working with FTIR, HPLC, LCMS, GCMS, ICPMS, NMR
Vast knowledge of following GMP guidelines and procedures
Willingness to train and develop team members
Experience Level
Intermediate Level
Pay and Benefits
The pay range for this position is $75000.00 - $85000.00/yr.
Company provides holiday, vacation, and 401k benefits. They will be able to gain bonuses past on company and personal performance.
Workplace Type
This is a fully onsite position in Tewksbury,MA.
Application Deadline
This position is anticipated to close on Sep 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 DescriptionThe Company We are Alloy Therapeutics—a biotechnology ecosystem company empowering the global scientific community to make better medicines together. Through a community of partners, we democratize access to pre-competitive tools, technologies, services, and company creation capabilities that are foundational for discovering and developing therapeutic biologics. The company facilitates affordable, non-exclusive access to the entire drug discovery community from academic scientists, small and medium biotech, to the largest biopharma. At Alloy, we believe our industry should compete on getting the best drugs to patients as quickly as possible, not exclusive access to the best platforms. As a reflection of our relentless commitment to the scientific community, we reinvest 100% of our revenue in innovation and access to innovation. MAY THE BEST DRUG WIN. Alloy is headquartered in Waltham, MA with additional labs in Cambridge, UK; Basel, Switzerland, and Athens, GA. Successful members thrive in our shared culture of accountability, deliberate trust, and open communication. As a team we aspire to work together to exceed expectations and collectively contribute across the global organization to always maintain our nimble, startup culture. This is an on-site and full-time position in Waltham, MA. At Alloy, we have an ethos of “Mentorship-By-Apprenticeship” in all of our positions.&nbsp;&nbsp;We strive to have workers in the office when needed to interact organically and face-to-face.&nbsp;&nbsp;Of course, as a lab-based operation, our cells and animals grow 7 days a week, 365 days per year.&nbsp;&nbsp;We respect and value our colleagues for their hard work that requires them to be in the lab every day.&nbsp;&nbsp;We ask our people who have more flexible accommodations, like this position, to appreciate their colleagues who have less flexibility.&nbsp;&nbsp;We are all one team! The Team Alloy’s In Vitro Pharmacology team collaborates with drug discovery partners to conduct in vitro studies on therapeutic candidates across diverse modalities. Our team delivers comprehensive functional screening and characterization of biologics to support discovery and selection of lead candidates. Primary modalities are monoclonal, multispecific, and TCR-mimic antibodies, but also include cell therapies and genetic medicines. As Alloy Tx enters its next phase of growth, we are expanding our capabilities to include mechanistic studies that enhance preclinical development and further advance our translational research efforts. The Role&nbsp; We are seeking a highly motivated Scientist for in vitro screening and pre-clinical development to join our dynamic and fast-paced team. In this role, you will support the execution of in vitro functional cell-based assays to evaluate the potency, mechanism of action, and pharmacological properties of biologic therapeutics. This role requires exceptional organizational skills, a commitment to scientific excellence, and the ability to adapt to a dynamic environment. You will report to the Head of In Vitro Pharmacology and will work collaboratively in a matrixed environment to drive biologics discovery while supporting rapid decision-making in a fast-moving biotech setting. How You’ll Drive Impact&nbsp;
<ul>
<li>Execute: Support in vitro functional characterization of drug candidate molecules.</li>
<li>Develop: Bring a proactive mindset to optimize workflows for more efficient and effective data generation.</li>
<li>Deliver: Support screening campaigns to meet experimental timelines for monoclonal and multispecific antibodies, as well as TCR-mimic antibodies.</li>
<li>Collaborate: Work closely across multi-disciplinary teams in biologics discovery programs spanning all Alloy sites. Engage with an inclusive and collaborative work environment.</li>
<li>Communicate: Clearly convey scientific concepts, experimental results, and interpretations to internal and external stakeholders.&nbsp;</li>
</ul>
 Principal Responsibilities&nbsp;
<ul>
<li>Expand, bio-bank and characterize primary and immortalized cell lines to validate target expression and enable downstream assays.</li>
<li>Generate engineered cell lines using lentiviral, CRISPR or other techniques.&nbsp;</li>
<li>Support day-to-day lab and experimental workflows, including cell line inventory maintenance.</li>
<li>Execute cell-based functional assays using high-throughput approaches in primary cells, immortalized reporter cell lines, and other disease-relevant cellular systems.</li>
<li>Process human leukopaks, isolate and characterize human PBMCs.</li>
<li>Present experimental data and findings during team meetings.</li>
<li>Ensure timely and successful execution of project activities according to plan.</li>
<li>Maintain detailed and accurate laboratory records in compliance with industry standards.</li>
<li>Maintain laboratory organization and ensure compliance with safety protocols.</li>
</ul>
 Qualifications
<ul>
<li>PhD in Cell or Molecular Biology, or a related field, with 0-2 years (Scientist I) or 3-5 years (Scientist II) of relevant industry experience.&nbsp;</li>
<li>Direct experience with cell line engineering (CRISPR, lentiviral, etc) required.</li>
<li>Flow cytometry and fundamental cell and molecular biology techniques required.</li>
<li>Significant cell culture experience with primary and immortalized cell lines.</li>
<li>Experience handling human blood, leukopak processing, and PBMC isolations.</li>
<li>Hands on experience isolating and/or expanding primary immune cell subsets preferred.</li>
<li>Direct experience with high-throughput cell-based assays a plus.</li>
<li>Experience with live cell imaging (i.e. Incucyte) a plus.</li>
<li>Excellent organization, clear communication and teamwork abilities in a multidisciplinary setting.&nbsp;</li>
<li>Thrives working on a team and collaborating with others to achieve project goals.</li>
<li>Enjoys a dynamic and exciting work environment.&nbsp;</li>
<li>Detail oriented, with rigorous scientific thinking and a passion for drug discovery to improve patients’ lives.</li>
</ul>
Taking Care of Our People We support the individuality of what people need to do outside of work to empower them to do their best at work. While you focus on making better medicine together, we focus on programs and benefits that support a diverse and growing team. Whether you’re single, in a growing family, or nearing retirement, Alloy offers a variety of comprehensive and competitive benefits starting from day one. Compensation
<ul>
<li>Competitive base and equity compensation commensurate with level of experience and independence</li>
<li>401(k) company match</li>
</ul>
Health &amp; Family
<ul>
<li>Generous personal and family medical, dental and vision benefits with 100% of premiums and deductibles covered</li>
<li>Company-paid disability (STD, LTD) and life insurance</li>
<li>Paid parental leave</li>
<li>Family planning support up to $45,000 (e.g., IVF/PGT, adoption, surrogacy, egg retrieval)</li>
</ul>
Unique Perks
<ul>
<li>Unlimited PTO (paid time off) and flexible schedules</li>
<li>Annual stipend for continuing education with commitment to your career through individualized professional development plan</li>
<li>Wellness and Extensive Employee Assistance Program (EAP) including resources for mental wellness</li>
</ul>
Pay Transparency At Alloy Therapeutics, we believe in fostering trust and open communication. For this role, the estimated annual base salary range is $130,000 - $145,000, with the final offer based on factors like your experience, skills, and alignment with our needs.
Additionally, this role is eligible for equity compensation, reflecting our commitment to shared success as we work together to make better medicines.
We are proud to offer competitive compensation and benefits, aiming to support our team’s professional and personal well-being. If you have any questions about pay or benefits, we’re here to help.
Alloy Therapeutics is an equal opportunity employer.&nbsp; All qualified applicants will receive consideration for employment without regard to race, color, religion, national origin, sex, sexual orientation, gender identity, veteran status, disability, or other legally protected status.&nbsp; If you are unable to submit an application because of incompatible assistive technology or a disability, please contact us at <a href="mailto:recruiting@alloytx.com" target="_blank">recruiting@alloytx.com</a>.&nbsp; We will make every effort to respond to your request for disability assistance as soon as possible. &nbsp;
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bKG7rjSEFO

Scientist I/II, In Vitro Pharmacology

<h3>Job Description</h3>
Job Description
Job Title:&nbsp;Metrologist Chemist
Location:&nbsp;Billerica, MA
Employment Type:&nbsp;Full Time - Permanent 
Experience Level:&nbsp;Intermediate
Overview:
We are seeking a skilled and detail-oriented&nbsp;Metrologist Chemist&nbsp;to support laboratory operations within a pharmaceutical manufacturing environment. This role focuses on ensuring all lab instrumentation is properly validated, calibrated, and compliant with GMP standards. The ideal candidate will have a strong foundation in chemistry and hands-on experience with lab equipment and quality systems.
Key Responsibilities:
<ul>
<li>Validate laboratory instrumentation and ensure alignment with approved analytical methods.</li>
<li>Author and maintain Standard Operating Procedures (SOPs).</li>
<li>Initiate and document deviations within the Quality Management System (QMS).</li>
<li>Coordinate calibration activities and collaborate with vendors to ensure equipment and method validation.</li>
<li>Follow SOPs and adhere to Good Manufacturing Practices (GMP).</li>
<li>Operate and maintain autoclaves and other lab instruments.</li>
</ul>
Required Skills &amp; Knowledge:
<ul>
<li>Chemistry and laboratory instrumentation expertise.</li>
<li>Experience with calibration, change control, and QMS documentation.</li>
<li>Familiarity with autoclaves, pH meters, and other analytical tools.</li>
<li>Proficiency with MasterControl, CMMS, and electronic document management systems (EDMs).</li>
<li>Hands-on experience with pH, conductivity meters, digital multimeters (DMM), and oscilloscopes.</li>
</ul>
Qualifications:
<ul>
<li>Associate degree in a life science discipline.</li>
<li>Minimum of 4 years of experience in a pharmaceutical manufacturing environment.</li>
<li>Strong attention to detail and ability to work independently and collaboratively.</li>
</ul>
Preferred Tools &amp; Platforms:
<ul>
<li>MasterControl</li>
<li>TrackWise</li>
<li>CMMS</li>
<li>EDMs</li>
</ul>
Pay and Benefits
The pay range for this position is $80000.00 - $91000.00/yr.
They get annual bonuses, they get holiday, vacation, as well as 401k and other medical benefits.
Workplace Type
This is a fully onsite position in Billerica,MA.
Application Deadline
This position is anticipated to close on Sep 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.

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