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<h3>Job Description</h3>
COMPANY OVERVIEW
AIRNA is a biotechnology company with a mission to be the leading RNA editing company delivering precision therapies to patients with rare and common diseases.
 
AIRNA is harnessing advances in genetics to develop transformative RNA-editing medicines that improve human health. Our proprietary platform is based on groundbreaking research by pioneers of the field and company co-founders Thorsten Stafforst (University of Tübingen) and Jin Billy Li (Stanford University) and enables optimal potency, safety, and delivery. AIRNA is advancing a robust pipeline of therapeutic candidates that are designed to provide functional cures for severe or chronic diseases by repairing harmful genetic variants or introducing beneficial variants promote optimal health.
 
AIRNA has raised $245 million in financing from a world-class syndicate of investors including Arch Venture Partners, Forbion, Venrock Healthcare Capital Partners, RTW Investments, Nextech Invest, and ND Capital. We value teamwork, resilience, excellence, human, and health, and have a diverse team at both our headquarters in Cambridge, MA and our research operations in Tübingen, Germany.
 
JOB DESCRIPTION
AIRNAis seeking a highly motivated Research Associate/Senior Research Associate to join our Preclinical Development team in Cambridge, MA and assist in executing activities associated with AIRNA's drug development programs advancing novel therapeutics to the clinic.
 
As a member of AIRNA’s Preclinical team, you will be involved in the development and execution of biochemical and cell-based assays for-RNA-modifying oligonucleotides. Your responsibilities will include:
 
<ul>
<li>Working independently or with minimal supervision to develop, and qualify biochemical and next generation sequencing-based assays.</li>
<li>Preparing RNA and proteins from cell or animal samples and analyzing these samples by qPCR, ELISA, MSD, next-generation sequencing, or Western blot analysis.</li>
<li>Generating detailed study summaries and preparing reports for regulatory submission.</li>
<li>Performing general lab duties such as maintenance of lab equipment and reagent preparations.</li>
<li>Maintaining accurate and complete records in an electronic notebook; preparing and updating documentation as needed (SOP, Batch Records, etc.).</li>
<li>Ensuring compliance with company policies, procedures, and safety regulations.</li>
<li>Being a positive, collaborative, and committed team member.</li>
</ul>
 
QUALIFICATIONS
<ul>
<li>Bachelor's degree in Biological Sciences, Biochemistry, Molecular Biology, or Pharmaceutical Sciences.</li>
<li>1 - 5 years of relevant working experience in industry. Experience in the field of oligonucleotide therapies is highly desirable.</li>
<li>Previous experience in oligonucleotide PK and PD assays.</li>
<li>Demonstrated ability to execute next generation sequencing-based assays, including primer design, PCR optimization, RT-qPCR, operation of a benchtop sequencer, and QC and basic processing of sequencing data.</li>
<li>Experience with aseptic laboratory technique required.</li>
<li>Timely and detailed experimental documentation.</li>
<li>Being detail-oriented with strong analytical and trouble-shooting skills.</li>
<li>Working familiarity with command line, Python, Microsoft Office, and PRISM.</li>
<li>Demonstrated ability to work as part of a team and to adapt within a fast-changing environment.</li>
</ul>
 
REQUIREMENTS
<ul>
<li>Biotechnology or pharmaceutical industry experience.</li>
<li>Experience in bioanalytical assay development and qualification based on regulatory guidelines.</li>
<li>Experience in using automatic liquid handlers and performing assays in 96+ plate formats.</li>
<li>Experience in sequencing library preparation and data processing.</li>
</ul>
 
LOCATION
AIRNA has a hybrid work model, and the role will be based in AIRNA’s corporate headquarters in Cambridge, MA ~4 days per week.

Research Associate / Senior Research Associate, Preclinical Development

<h3>Job Description</h3>
Job Description
Our client, a leading innovator in the food industry, is seeking a Research &amp; Development Tech to join their team. As a Research &amp; Development Tech, you will be part of the R&amp;D department supporting product development and process optimization teams. The ideal candidate will have curiosity, problem-solving skills, and a collaborative mindset which will align successfully in the organization.
Job Title: Research &amp; Development Tech
Location: Quincy, MA
Pay Range: $20 - $23 per hour
Shift: 8:00am to 5:00pm Monday to Friday
What's the Job?
<ul>
<li>Conduct research including new product development and food formulation</li>
<li>Develop new and improved methods for food processing, quality control, and packaging</li>
<li>Support pilot plant activities and assist with production scale-ups and commercialization efforts</li>
<li>Address customer requests from conceptualization through troubleshooting and commercialization</li>
<li>Collaborate with culinary and subject matter experts to develop standards and optimize formulations</li>
</ul>
What's Needed?
<ul>
<li>Basic understanding of food science and processing techniques</li>
<li>Strong communication skills for technical and culinary presentations</li>
<li>Ability to troubleshoot and understand customer processes</li>
<li>Experience in research documentation and process improvement</li>
<li>Motivation to innovate and contribute to product excellence</li>
</ul>
What's in it for me?
<ul>
<li>Opportunity to work in a dynamic and innovative environment</li>
<li>Engage in meaningful research that impacts product quality and customer satisfaction</li>
<li>Collaborate with cross-functional teams and industry experts</li>
<li>Develop your skills in food science and product development</li>
<li>Be part of a company committed to nourishing and delighting customers</li>
</ul>
Upon completion of waiting period associates are eligible for:
<ul>
<li>Medical and Prescription Drug Plans</li>
<li>Dental Plan</li>
<li>Supplemental Life Insurance</li>
<li>Short Term Disability Insurance</li>
<li>401(k)</li>
</ul>
If this is a role that interests you and you'd like to learn more, click apply now and a recruiter will be in touch with you to discuss this great opportunity. We look forward to speaking with you!
About ManpowerGroup, Parent Company of: &nbsp;Manpower, Experis, Talent Solutions, and Jefferson Wells
ManpowerGroup® (NYSE: MAN), the leading global workforce solutions company, helps organizations transform in a fast-changing world of work by sourcing, assessing, developing, and managing the talent that enables them to win. We develop innovative solutions for hundreds of thousands of organizations every year, providing them with skilled talent while finding meaningful, sustainable employment for millions of people across a wide range of industries and skills. Our expert family of brands – Manpower, Experis, Talent Solutions, and Jefferson Wells –&nbsp;creates substantial value for candidates and clients across more than 75 countries and territories and has done so for over 70 years. We are recognized consistently for our diversity - as a best place to work for Women, Inclusion, Equality and Disability and in 2023 ManpowerGroup was named one of the World's Most Ethical Companies for the 14th year - all confirming our position as the brand of choice for in-demand talent.

Research & Development Tech

<h3>Job Description</h3>
Job Description
For more than 50 years, EdgeTech has been the industry leader in the design and manufacture of advanced underwater sonar systems for applications involving seabed survey, target detection, object identification, mooring instrumentation, and acoustic tracking/positioning.&nbsp; Our products are used to support a variety of customers, from offshore oil and gas to fisheries/science/underwater research, defense, and police/fire search and rescue
We’re looking for an engineer/scientist with interest in applying signal processing to develop algorithms that enable new capabilities in next-generation sonar systems. Typical assignments include algorithm design, analysis, and implementation; sonar system analysis; involvement in software and hardware prototyping and test activities; documentation and planning; as well as sea testing, data collection, and post-trial analysis.
Job Responsibilities
<ul>
<li>Design algorithms for processing of sonar signals including waveform design, beamforming, broadband processing, and detection.</li>
<li>Develop processing algorithms and assess their performance. Interpret results.</li>
<li>Collaborate with real-time code developers and modeling/simulation analysts to develop and integrate system software.</li>
<li>Develop simple and reliable signal processing algorithms for a variety of processors, to include ARM’s, SoC’s/SoM's and FPGAs</li>
<li>Assist with the development of signal processing specifications and their implementation</li>
<li>Test software, firmware and full sonar solutions in simulation, hardware-in-the-loop, and field demonstrations</li>
<li>Collaborate with a cross-functional team testing your contributions and analyzing performance</li>
<li>Support the engineering, production, and sales/marketing teams with productization of technologies and solutions</li>
<li>Understand broad product objectives to develop and maintain relationships with major customers.</li>
<li>Collaborate with other engineers, customers and the technical community to advance sonar capabilities for current and future applications</li>
</ul>
Job Requirements
<ul>
<li>This job can be filled at multiple levels, depending upon the successful candidate’s education and experience. Minimum education required is an M.S. degree in an engineering or science related discipline plus five year’s related experience or an equivalent combination of education and experience.</li>
<li>Experience with signal processing theory and applications</li>
<li>Experience with scripting and analysis tools such as Matlab and Python</li>
<li>Experience with planning and conducting sea trials and surveys.</li>
<li>Highly effective written and verbal communication skills</li>
<li>Ability to work effectively in a team and set priorities</li>
<li>Work with sonar imaging technologies or hydrographic applications is a big plus.</li>
<li>Familiarity with hardware (amplifiers, antennas/transducers, filters), and digital processing with FPGAs, GPUs, CPUs, is desirable but not required.</li>
<li>Work will include a mix of field and office assignments, with domestic and international travel as part of the job.</li>
</ul>
If interested, please contact:
Kevin Igo
<a href="mailto:Kevin.Igo@edgetech.com" target="_blank">Kevin.Igo@edgetech.com</a>
Company DescriptionEdgeTech is a leading manufacturer of underwater technology solutions. The company is known worldwide for its high quality products which include: side scan sonars, sub-bottom profilers, bathymetry systems, AUV and ROV-based sonar systems, combined and customized solutions. In addition to the full line of underwater survey products, EdgeTech provides reliable USBL systems, transponder beacons, deep sea acoustic releases, shallow water and long life acoustic releases, MRUs and customized underwater acoustic command and control systems. 
<h3>Company Description</h3>
EdgeTech is a leading manufacturer of underwater technology solutions. The company is known worldwide for its high quality products which include: side scan sonars, sub-bottom profilers, bathymetry systems, AUV and ROV-based sonar systems, combined and customized solutions. In addition to the full line of underwater survey products, EdgeTech provides reliable USBL systems, transponder beacons, deep sea acoustic releases, shallow water and long life acoustic releases, MRUs and customized underwater acoustic command and control systems.

Applied Research Scientist

<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 
The Lead Purification Scientist will lead a team of scientists and analysts in executing small-scale purification studies to support biopharmaceutical manufacturing processes. This role combines hands-on technical expertise with leadership responsibilities, ensuring high-quality data generation, documentation, and cross-functional collaboration. The Group Leader will drive innovation, manage project timelines, and support technology transfer activities.
Key Responsibilities:
Technical Expertise:
<ul>
<li>Design and execute small-scale purification studies using chromatography, ultrafiltration/diafiltration (UF/DF), tangential flow filtration (TFF), and sterile/depth filtration techniques.</li>
<li>Operate and troubleshoot chromatography systems (e.g., AKTA) and associated software (Unicorn) for experimental purification runs.</li>
<li>Perform essential lab support tasks, including solution preparation, sample submission, and equipment calibration.</li>
<li>Analyze complex datasets using statistical tools and author detailed technical reports to support study conclusions.</li>
<li>Present findings in cross-functional meetings and actively contribute to scientific and strategic discussions.</li>
<li>Lead purification efforts for assigned projects, ensuring thorough planning, execution, and documentation.</li>
<li>Collaborate with cross-disciplinary teams to align lab activities with broader project goals.</li>
<li>Maintain compliance with GxP standards, GHS policies, and internal protocols.</li>
<li>Manage multiple concurrent projects, prioritize tasks effectively, and communicate progress across teams.</li>
</ul>
Leadership &amp; Team Development:
<ul>
<li>Supervise a team of analysts, ensuring timely and high-quality execution of laboratory work.</li>
<li>Participate in recruitment efforts, including candidate interviews and hiring decisions.</li>
<li>Lead onboarding and training initiatives for new team members; provide ongoing mentorship and skill development.</li>
<li>Conduct performance evaluations and deliver constructive feedback to support professional growth.</li>
<li>Monitor team workload and optimize resource allocation to meet project timelines.</li>
<li>Engage in leadership development and foster a culture of continuous improvement and scientific excellence.</li>
</ul>
Qualifications 
Education &amp; Experience:
<ul>
<li>Bachelor’s degree in chemistry, biology, pharmacy, engineering, or related field with 3+ years of relevant industry experience, or Master’s degree with 1+ years of experience.</li>
<li>Hands-on experience with downstream purification processes in pilot-scale or R&amp;D environments.</li>
<li>Familiarity with AKTA systems and Unicorn software preferred.</li>
</ul>
Technical Skills:
<ul>
<li>Strong documentation and organizational capabilities.</li>
<li>Proficient in lab equipment operation and data interpretation.</li>
<li>Experience troubleshooting downstream processes such as chromatography, UF/DF, and filtration.</li>
<li>Exposure to scale-up, tech transfer, and GMP manufacturing support.</li>
<li>Knowledge of upstream processing is a plus.</li>
<li>Experience with tools such as Solo VPE, JMP, Viper, BioSMB, PALL System Software, Pendotech, and Microsoft Office.</li>
</ul>
Additional Requirements:
<ul>
<li>Excellent communication and time management skills.</li>
<li>Comfortable working in both collaborative (60%) and independent (40%) settings.</li>
<li>Physically capable of lifting/pushing up to 75 lbs, standing for extended periods, and working on platforms/ladders.</li>
<li>Must be authorized to work in the United States indefinitely without restriction or sponsorship.</li>
</ul>
 Additional Information 
Position is&nbsp;Full Time, Monday-Friday, First Shift, Monday through Friday from 8 am-4:30 pm&nbsp;Candidates currently living within a commutable distance of Framingham, MA,&nbsp;are encouraged to apply
Excellent full-time benefits include:&nbsp;
<ul>
<li>Medical Coverage:&nbsp;Comprehensive medical insurance options</li>
<li>Dental &amp; Vision:&nbsp;Full dental and vision coverage available</li>
<li>Life &amp; Disability Insurance:&nbsp;Employer-sponsored plans</li>
<li>Retirement:&nbsp;401(k) plan with company match</li>
<li>Paid Time Off:&nbsp;Vacation days, paid holidays, and additional PTO options</li>
<li>Compensation: $42.00 - 47.00 per hour
<ul>
<li>$87,360–$97,760 annually&nbsp;</li>
</ul>
</li>
</ul>
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Lead Purification Scientist - Bioprocess Development

<h3>Job Description</h3>
Job DescriptionCompany Description 
The work we do at Eurofins matters, and so do our employees. At Eurofins, 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, apply with us today!&nbsp;&nbsp;
Job Description 
<ul>
<li>Contributes as part of a small team towards the execution and development of various analytical methods to support biological therapeutic characterization testing in a research-based environment.</li>
<li>Works closely with adjacent team members to collaborate and reach collective goals related to study designs and organization of shared lab space.</li>
<li>Method development and execution related work, as well as associated documentation and regular assay troubleshooting.</li>
<li>Performs protein characterization testing as assigned, such as glycan analysis and disulfide mapping, and other types of analyses to include proteomics, intact protein, subunit, and peptide mapping.</li>
<li>Computer competency is essential with emphasis on spreadsheet-based software.</li>
<li>Uses the Protein Metrics software (Byos or Byosphere) to view and analyze MS data.</li>
<li>Supports drug development projects and regulatory submissions, such as IND and BLA filings.</li>
<li>Understands and applies the advanced scientific principles, theories and concepts, practices and standards for product development.</li>
<li>Conducts work in compliance with GLP, safety and regulatory requirements.</li>
<li>Provides routine updates to client via progress presentations and is responsible for following up on project deadlines and other agreed objectives.</li>
<li>Demonstrates independent judgment in technique and method selection, protocol and study design and execution, data analysis and use of standard practices and procedures for a variety of problems of moderate scope and complexity to meet assigned objectives.</li>
</ul>
Qualifications 
<ul>
<li>Candidate must have a degree in Chemistry (Analytical or Organic), Biochemistry, Pharmaceutical, or other biological/analytical discipline, along with the following experience in biotechnology, pharmaceutical, or related environment:</li>
<li>BS (8-12 yrs exp); Engineer (6-10 yrs exp); MS (6-10 yrs exp); or PhD (2-5 yrs exp): &nbsp;
<ul>
<li>Experience working with one or more oft he following methods: intact protein, subunit, and peptide mapping analyses, proteomics, etc., is a must.</li>
<li>Hands-on LC-MS experience using a Thermo Orbitrap mass spectrometer is a must.</li>
<li>Experience working with Mass Spectroscopy instrumentation and software like Protein Metrics (Byos or Byosphere) is preferred.</li>
<li>Experience working with one or more of following protein characterization methods: glycan analysis, disulfide mapping, etc is a plus</li>
</ul>
</li>
<li>Understanding of basic scientific principles and theories of one of the techniques within LCMS/MS and protein characterization techniques is a must</li>
<li>Knowledge of theories, principles and techniques of relevant scientific areas and basic understanding of industry practices and standards is required</li>
<li>Strong computer, scientific, and organizational skills</li>
<li>Excellent communication (oral and written) and attention to detail</li>
<li>Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude</li>
<li>Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies</li>
<li>Authorization to work in the United States indefinitely 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 Meeting Onsite to Meet the Team&nbsp;</li>
</ul>
Position is&nbsp;Full Time, Monday-Friday, First Shift, Monday through Friday from 8 am-5 pm&nbsp;Candidates currently living within a commutable distance of&nbsp;Lexington, MA,&nbsp;are encouraged to apply
Excellent full-time benefits include:&nbsp;
<ul>
<li>Medical Coverage:&nbsp;Comprehensive medical insurance options</li>
<li>Dental &amp; Vision:&nbsp;Full dental and vision coverage available</li>
<li>Life &amp; Disability Insurance:&nbsp;Employer-sponsored plans</li>
<li>Retirement:&nbsp;401(k) plan with company match</li>
<li>Paid Time Off:&nbsp;Vacation days, paid holidays, and additional PTO options</li>
<li>Compensation:&nbsp;$100,000 - $107,000 annually&nbsp;&nbsp;</li>
</ul>
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Biologics LCMS Development Scientist

<h3>Job Description</h3>
Job Description
Description
<ul>
<li>Support development and research of new methods and analytical techniques to be used to release new and existing products </li>
<li>Validation and verification of analytical methods</li>
<li>perform investigations of out of specification, out of trends, equipment failure, etc. </li>
<li>Present trending data to support development and validation following GMP guidelines</li>
<li>Perform analytical testing for organic and inorganic chemicals by using FTIR, HPLC, NMR LCMS, GCMS, ICP- MS, GC and wet chemistry</li>
<li>Create test procedures and provide analytical support for certain research products</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>MS in chemistry or biochemistry with 3-5 years experience or a BS with 5-7 years experience</li>
<li>Experience working with FTIR, HPLC, LCMS, GCMS, ICPMS, NMR</li>
<li>Vast knowledge of following GMP guidelines and procedures</li>
<li>Willingness to train and develop team members</li>
</ul>
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 26, 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 DescriptionNow Hiring: Analytical Bench Chemist – Food Industry
Hadley, MA 
Summary:
Are you passionate about science, precision, and food innovation? Join our dynamic team as an Analytical Bench Chemist, where you'll play a key role in ensuring the safety, quality, and consistency of our food ingredients and products.
This is a hands-on laboratory role ideal for someone who thrives in a fast-paced environment and enjoys solving complex analytical challenges. You’ll work closely with cross-functional teams in R&amp;D, Quality, and Production to support product development and ensure regulatory compliance.
 Job Details:
<ul>
<li>Perform routine and non-routine chemical analyses on raw materials, in-process samples, and finished products using techniques such as HPLC, GC, UV-Vis, FTIR, titration, and more.</li>
<li>Develop, validate, and optimize analytical methods to support product innovation and quality assurance.</li>
<li>Maintain and calibrate laboratory instruments and ensure compliance with GLP/GMP standards.</li>
<li>Document results accurately and prepare detailed reports for internal and regulatory use.</li>
<li>Collaborate with QA and R&amp;D teams to troubleshoot formulation or process-related issues.</li>
<li>Support regulatory submissions and ensure compliance with FDA, USDA, and other relevant standards.</li>
<li>Participate in internal audits and contribute to continuous improvement initiatives.</li>
</ul>
Requirements:
<ul>
<li>Bachelor’s or Master’s degree in Chemistry, Food Science, Biochemistry, or related field.</li>
<li>2–5 years of experience in an analytical chemistry role, preferably in the food, beverage, or nutraceutical industry.</li>
<li>Strong proficiency in instrumental analysis (HPLC, GC, etc.) and wet chemistry techniques.</li>
<li>Familiarity with FDA regulations, food safety standards, and laboratory best practices.</li>
<li>Excellent attention to detail, organizational skills, and ability to work independently.</li>
<li>Strong communication skills and a collaborative mindset.</li>
</ul>
Why Join Us?
We’re a science-driven food company committed to innovation, sustainability, and quality. As part of our team, you’ll have the opportunity to work on exciting projects, grow your career, and make a meaningful impact on the food industry.
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 26, 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 DescriptionJob Title: Manufacturing Chemist II
Job Description
We have multiple openings for the position of Manufacturing Chemist II across 1st, 2nd, and 3rd shifts. This role offers a dynamic opportunity for career growth within a thriving Contract Manufacturing Organization (CMO) in the biotech industry.
Responsibilities
<ul>
<li>Maintain a clean, organized, and safe work environment in compliance with GMP standards and safety protocols.</li>
<li>Proactively identify and report safety hazards and incidents.</li>
<li>Accurately complete GMP documentation and review basic records such as logbooks.</li>
<li>Assist in revising procedures under direct supervision.</li>
<li>Participate in investigations and support execution of CAPA (Corrective and Preventive Actions).</li>
<li>Contribute to small-scale continuous improvement initiatives.</li>
<li>Perform assigned production activities, ensuring all required training is completed and compliant prior to operations.</li>
<li>Apply basic problem-solving skills to identify abnormal results and escalate issues appropriately.</li>
<li>Demonstrate proficiency in designated process areas.</li>
</ul>
Essential Skills
<ul>
<li>Proficiency in pH testing, aseptic technique, buffer preparation, UV Vis spectrophotometry, and general Chemistry.</li>
<li>Experience with GMP, UV Vis, and pH Meter operations.</li>
<li>Knowledge of purification, chromatography, and biotechnology processes.</li>
<li>Two plus years of experience in a cGMP manufacturing environment.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Minimum education requirements: high school diploma or equivalent.</li>
<li>Preferred: college-level Chemistry degree or equivalent work experience.</li>
<li>A biotechnology certificate or college degree is preferred.</li>
<li>Knowledge of basic laboratory instrumentation such as use of pH meter, UV instrumentation, and solution delivery systems (process skids).</li>
</ul>
Work Environment
You will be working in a GMP-based environment with a team that values teamwork and camaraderie. The atmosphere is easygoing yet focused on productivity, allowing for a balance of fun and professionalism. Shifts available are: 1st Shift, 2nd Shift with a 15% shift differential, and 3rd Shift with a 20% shift differential. Our close-knit team is committed to making a difference in the biotech industry, offering a chance to be part of an innovative and exciting work setting.
Pay and Benefits
The pay range for this position is $61700.00 - $75600.00/yr.
Health insurance, 401k, PTO, 12 Paid holidays
Workplace Type
This is a fully onsite position in Milford,MA.
Application Deadline
This position is anticipated to close on Sep 30, 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.

Manufacturing Chemist II

<h3>Job Description</h3>
Job DescriptionJob Title: Quality Control Chemist
Job Description
The Quality Control Chemist will support method development for GC, HPLC, and UPLC and engage in analytical chemistry work. The role involves identifying and performing proper characterization methods and writing, preparing, and presenting technical data, reports, and standard operating procedures (SOPs) for internal use.
Responsibilities
<ul>
<li>Support method development for GC, HPLC, and UPLC.</li>
<li>Perform analytical chemistry work.</li>
<li>Identify and implement appropriate characterization methods.</li>
<li>Write, prepare, and present technical data, technical reports, and SOPs for internal use.</li>
<li>Execute and oversee chemistry methods to support the chemistry team.</li>
<li>Drive research and development within the department.</li>
</ul>
Essential Skills
<ul>
<li>Proficiency in Chemistry, HPLC, UPLC, and method development.</li>
<li>Experience with analytical chemistry, gas chromatography, capillary electrophoresis, conductivity, FTIR, GCMS, UVVIS, and wet chemistry.</li>
<li>Quality control expertise.</li>
<li>Hands-on experience with empower systems.</li>
<li>Experience with CE methods, such as CE-SDS and cIEF, for analyzing biological materials.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Bachelor's or Master's degree in Chemistry, Biochemistry, or related field.</li>
<li>3-5 years of experience in method development with various chemistry instrumentation.</li>
<li>Detail-oriented, collaborative, and hardworking.</li>
</ul>
Work Environment
The position requires 100% onsite work in the Quality Control chemistry group. The work environment is business casual, with a first shift schedule from Monday to Friday. The team values individuals who are detail-oriented, collaborative, and dedicated to their work.
Job Type &amp; Location
This is a Contract position based out of Bedford, Massachusetts.
Pay and Benefits
The pay range for this position is $35.00 - $40.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
 • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Bedford,MA.
Application Deadline
This position is anticipated to close on Sep 25, 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.

Quality Control Chemist

<h3>Job Description</h3>
Job DescriptionJob Title: Quality Control Chemist
Job Description
The Quality Control Chemist will support method development for GC, HPLC, and UPLC and engage in analytical chemistry work. The role involves identifying and performing proper characterization methods and writing, preparing, and presenting technical data, reports, and standard operating procedures (SOPs) for internal use.
Responsibilities
<ul>
<li>Support method development for GC, HPLC, and UPLC.</li>
<li>Perform analytical chemistry work.</li>
<li>Identify and implement appropriate characterization methods.</li>
<li>Write, prepare, and present technical data, technical reports, and SOPs for internal use.</li>
<li>Execute and oversee chemistry methods to support the chemistry team.</li>
<li>Drive research and development within the department.</li>
</ul>
Essential Skills
<ul>
<li>Proficiency in Chemistry, HPLC, UPLC, and method development.</li>
<li>Experience with analytical chemistry, gas chromatography, capillary electrophoresis, conductivity, FTIR, GCMS, UVVIS, and wet chemistry.</li>
<li>Quality control expertise.</li>
<li>Hands-on experience with empower systems.</li>
<li>Experience with CE methods, such as CE-SDS and cIEF, for analyzing biological materials.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Bachelor's or Master's degree in Chemistry, Biochemistry, or related field.</li>
<li>3-5 years of experience in method development with various chemistry instrumentation.</li>
<li>Detail-oriented, collaborative, and hardworking.</li>
</ul>
Work Environment
The position requires 100% onsite work in the Quality Control chemistry group. The work environment is business casual, with a first shift schedule from Monday to Friday. The team values individuals who are detail-oriented, collaborative, and dedicated to their work.
Job Type &amp; Location
This is a Contract position based out of Bedford, Massachusetts.
If interested, please reach out directly to Lindsee Allienello at lallienello @ actalentservices.com. 
Pay and Benefits
The pay range for this position is $35.00 - $40.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
 • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Bedford,MA.
Application Deadline
This position is anticipated to close on Sep 26, 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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