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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
AIRNA is 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>
We are a Boston-area biomedical diagnostics startup company seeking a Clinical Blood Biochemist/Microbiologist to join our team.
Your mission will be to apply your biochemistry and microbiology expertise in support of developing rapid clinical diagnostics. Working closely with a multidisciplinary team spanning many fields of expertise, from medical microbiology to machine learning, you will take the lead designing, executing, and interpreting experiments involving blood-borne pathogens and biochemical growth conditions—helping advance diagnostics that improve patient outcomes around the globe.
Required Qualifications
<ul>
<li>Master’s degree or PhD in biochemistry, microbiology, or a related life sciences field</li>
<li>2+ years of wet-lab experience, ideally in a BSL2 and/or clinical laboratory setting</li>
<li>Hands-on experience with microbial culturing, gram staining, and antimicrobial susceptibility testing</li>
<li>Experience designing and conducting experiments involving growth of bacteria and fungi in blood and/or blood-derived growth media</li>
<li>Deep understanding of blood chemistry, including pH, blood additives (e.g. anticoagulants), and blood components (molecular and cellular)</li>
<li>Skilled in preparing and managing blood cultures and growth assays for clinically relevant organisms</li>
<li>Excellent documentation habits and experience writing and maintaining SOPs and lab protocols</li>
<li>Strong organizational and communication skills, both written and verbal</li>
<li>Commitment to accuracy, quality control, and laboratory safety standards</li>
</ul>
Preferred Qualifications
<ul>
<li>Experience supporting or working alongside clinical microbiologists in a diagnostic or research setting</li>
<li>Familiarity with laboratory instrumentation for microbial growth and analysis (e.g. incubators, anaerobic chambers, spectrophotometers)</li>
<li>Experience with fungal identification or culturing in clinical matrices</li>
<li>Exposure to automated microbial identification tools or molecular platforms (e.g. MALDI-TOF, BioFire)</li>
<li>Familiarity with basic programming or data analysis tools (Python, R, Excel macros, etc.)</li>
</ul>
Particulars
<ul>
<li>Company headquarters: Beverly, MA; on-site work preferred</li>
<li>Competitive salary and equity compensation package</li>
<li>Comprehensive health benefits and flexible paid time off</li>
</ul>
Why Join Us?
You could take your training and experience to a big-name institution or multinational—but if you’d rather be on a close-knit team of innovators who actually build and ship life-saving technologies, you might find your home here. You’ll be a core part of a team that values creativity, urgency, precision, and purpose.
If that resonates, please send a short (~250-word) cover letter and resume/CV to <a href="mailto:careers@astradx.com" target="_blank">careers@astradx.com</a>. Feel free to include any links to lab notebooks, GitHub, protocols you’ve authored, or other relevant work.
Note: Your cover letter should include:
<ul>
<li>Why you’re interested in this particular role and company (~100 words)</li>
<li>One experiment, technique, or scientific idea you’ve come across recently that you found fascinating (~100 words)</li>
</ul>
Let me know if you'd like a version for internal use (e.g. hiring manager spec) or edited for a different platform like LinkedIn or academic job boards.
&nbsp;

Clinical Blood Biochemist/Microbiologist at Biomedical Diagnostics Startup

<h3>Job Description</h3>
Job Description
Title: Spring Drug Discovery Biology Co-Op/Internship
Location: Downtown Boston, MA (on-site 5 days/week)
Duration: January-June 2026
Hourly Rate: $20-$30/hr, dependent on experience 
Weekly Hours: 30-40 hours/week
Job Summary: 
Antares Therapeutics is seeking a highly motivated co-op/intern student to join the Drug Discovery Biology team for the Spring semester of 2026. This candidate will serve a critical role in helping establish cell-based assays to inform target biology, in addition to supporting translational biology efforts. This position is ideal for a talented, highly motivated and results driven individual who will thrive in a fast-paced, innovative, start-up environment.
Key Responsibilities:
<ul>
<li>Maintain human tumor cell lines in tissue culture (thawing, freezing, splitting cell lines). New CRISPR and lentiviral engineered cell lines are regularly being developed (e.g. knockout and knock-in mutation/insertions) that require maintenance such as pools and sub-cloning. This will be a great opportunity for the co-op/intern student to gain valuable TC experience and exposure to cell line engineering.</li>
<li>The co-op/intern student will assist in cellular assays and studies to help elucidate mechanism of action (MoA), with a focus on cell growth (proliferation) and biomarkers (TR-FRET, AlphaLISA, Western blot, ELISA).</li>
<li>The co-op/intern student will gain experience with the design, optimization, and execution of cellular assays, data analysis and communication of results in a team environment.</li>
<li>The co-op/intern student will learn documentation of experimental results in an electronic notebook and the use of data analysis and data archive systems.</li>
<li>The co-op/intern candidate will learn automation workflow procedures that support programs across the portfolio.
<ul>
<li>The co-op/intern student will gain exposure to using equipment such as the Echo, PHERAstar, Bravo, and MultiDrop Combi.</li>
</ul>
</li>
<li>The co-op/intern student will gain valuable experience working in a collaborative team environment and interactions that contribute to a positive work environment, including safety, lab hygiene, and general lab duties such as stocking and reagent preparation.</li>
</ul>
Basic Requirements:
<ul>
<li>Current undergraduate student studying Biology or a related field</li>
<li>Fundamental understanding of basic biology concepts realized through lab work or relevant coursework</li>
<li>Experience with basic lab techniques is a plus (preparing buffers/solutions and dilutions, pipetting, and sterile technique; experience with PCR, gel electrophoresis, western blotting, and/or tissue culture is a plus); such experience may have been realized through a lab course or a prior internship.</li>
</ul>

Spring Drug Discovery Biology Co-Op/Internship

<h3>Job Description</h3>
Nabla Bio is building AI capable of generating biomolecules on demand to probe and treat disease. By combining cutting-edge AI with experimental systems that reflect how drugs behave in humans, we’re designing new kinds of medicines — targeting biology conventional tools can’t reach, and in drug formats built for disease precision, safety, and human impact. Backed by premier investors like Radical and Khosla Ventures, we have forged significant partnerships with leading pharma companies such as AstraZeneca, Takeda, and Bristol Myers Squibb.
 
The Role
Fueled by partnerships and increasing demand for internal R&amp;D, we will be looking to you to help scale our antibody expression, purification, and developability measurement pipeline and apply it toward solving hard antibody design problems. This will include:
<ul>
<li>Developing high-throughput HEK and CHO-based antibody expression and purification protocols.</li>
<li>Prioritizing top development candidates by characterizing antibodies for key biophysical traits, including but not limited to, affinity, cross-reactivity, stability, polyspecificity, aggregation, and hydrophobicity</li>
<li>Performing and improving molecular biology workflows including cloning, PCR, Gibson/Golden Gate assembly, DNA sequencing, and bacterial transformation.</li>
<li>Working together with our dry-lab and other wet-lab scientists to establish a rapid and seamless production and testing pipeline for characterizing machine learning generated antibody designs</li>
<li>This role has a strong focus on process development and workflows.</li>
</ul>
 
Qualifications
You are a strong candidate if you have led successful multi-month/year projects featuring direct experience in the above.
<ul>
<li>Life science-focused MS or BS with 1-2 years research/industry experience are highly desirable.</li>
<li>You must like to work quickly with precision. High aptitude, tenacity, and the foundational knowledge to solve problems outside of your comfort zone is critical.</li>
<li>We will invest heavily in training you, and are committed to helping you grow within Nabla and beyond.</li>
</ul>
 
What We Offer
<ul>
<li>A fast-moving environment where you can build and ship tools that impact real drug programs</li>
<li>A small, focused team where your scientific and engineering decisions have outsized impact</li>
<li>Highly competitive salary, equity, and benefits package</li>
</ul>
 
Nabla Bio is an equal opportunity employer. We welcome applicants from all backgrounds and experiences, and strongly encourage candidates from underrepresented groups in science and technology to apply. Reach out at <a href="mailto:hiring@nabla.bio" target="_blank">hiring@nabla.bio</a>.

Protein Production & Characterization (RA/Scientist, entry)

<h3>Job Description</h3>
Job Descriptionjob summary: 
The Chemist is an individual contributor responsible for performing a variety of tests on samples within a Quality Control (QC) laboratory. This role involves operating and maintaining various instruments, ensuring data integrity, and adhering to strict cGMP and documentation practices. The specific duties and responsibilities may vary based on the assigned department, group, as well as the individual's education, training, and level of experience. This position requires a strong working knowledge of analytical techniques and equipment to ensure the quality and compliance of all tested materials. 3+ years of experience in analytical testing within a cGMP environment or a Quality Control (QC) lab is required. 
FLSA Classification: Full-Time
Work Location: Fall River, MA
Work Hours: General Shift: 8:30AM - 5:00PM (may vary based on business needs)
 location: Fall River, Massachusetts job type: Permanent salary: $70,000 - 90,000 per year work hours: 9 to 5 education: Bachelors responsibilities: 
<ul>
<li>Execute a full range of analytical testing, including routine, advanced, and critical analysis, with a working knowledge of raw materials testing and release.</li>
<li>Operate and maintain a variety of specialized instruments, such as Karl Fischer, HPLC, GC, Particle Size, and ICP, and coordinate with vendors for their installation and qualification.</li>
<li>Ensure strict compliance with all cGMP (current Good Manufacturing Practices), data integrity, and good documentation practices.</li>
<li>Lead investigation activities to address testing deviations or other issues as they arise.</li>
</ul>
 qualifications: 
Required:
<ul>
<li>Bachelor's degree (BS or BA) in scientific discipline</li>
<li> 3+ years of experience in analytical testing within a cGMP environment or a Quality Control (QC) lab </li>
</ul>
Preferred:
<ul>
<li> Experience in Inhalation products (MDI)</li>
</ul>
 #LI-AB1 
 skills: High Pressure Liquid Chromatography (HPLC), Gas Chromatography (GC) 
 Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact <a href="mailto:HRsupport@randstadusa.com" target="_blank">HRsupport@randstadusa.com</a>. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&amp;D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility). This posting is open for thirty (30) days. It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

QC Chemist II

<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
&nbsp;
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.
&nbsp;
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>
&nbsp;
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>
&nbsp;
If interested, please contact:
&nbsp;
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.

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