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city

state

<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
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 DescriptionTitle: Research Associate, Antibody &amp; Protein Engineering
 Adimab is the leading technology provider for therapeutic antibody drug discovery, focusing solely on our partnerships without pursuing an internal product pipeline. Since 2009, we have partnered with over 130 pharmaceutical and biotechnology companies, generating more than 600 therapeutic programs, of which more than 75 have entered clinical trials.&nbsp;&nbsp;
Role Overview: We are seeking a focused and enthusiastic protein engineer to join our Platform Technologies group. In this role, the Research Associate will work in a small, collaborative team to execute Adimab’s platform for the discovery, optimization and characterization of protein-based therapeutics.
Responsibilities:&nbsp;
<ul>
<li>Designing and executing protein engineering experiments</li>
<li>Constructing yeast display libraries and performing FACS selections</li>
<li>Basic protein/DNA sequence and structural analysis</li>
<li>Basic yeast handling and propagation</li>
<li>Collecting, organizing, and analyzing antibody characterization data</li>
<li>Collaborating with colleagues and external partners &nbsp;</li>
</ul>
Needed Upon Hire:
<ul>
<li>B.S., or equivalent practical experience, with training in molecular biology, chemical engineering, or biochemistry</li>
<li>At least 2 years of lab experience in an academic or industry setting&nbsp;</li>
<li>Knowledge of molecular biology, protein engineering, structural biology, and/or flow cytometry</li>
<li>Meticulous approach to benchwork and data analysis &nbsp;</li>
</ul>
Value-added Experience:
<ul>
<li>Experience with protein display technologies (yeast, bacterial and/or ribosomal) desired</li>
<li>Knowledge of protein sequence analysis and next-generation sequencing workflows desired</li>
<li>Experience with protein structural analysis or computational design methods desired</li>
<li>Demonstrated ability to evaluate, interpret, and present scientific data</li>
<li>Internally motivated with proven track record of operating independently at the bench and bringing projects to completion</li>
<li>Excellent organization skills and the ability to manage multiple projects simultaneously</li>
<li>Adaptable and productive in a fast-paced environment</li>
<li>Communicates effectively and openly with colleagues and supervisors</li>
<li>Resourceful with outstanding execution and problem-solving skills</li>
<li>Excellent quantitative skills with a mastery of Excel</li>
</ul>
 Come join us! Our integrated antibody discovery and engineering platform provides unprecedented speed from antigen to purified, full-length human IgGs with exquisite specificity and biophysical behavior. We offer&nbsp;fundamental advantages by delivering diverse panels of antibodies that meet the most demanding standards for affinity, epitope specificity, species cross-reactivity, and developability. We enable our partners to rapidly expand their biologics pipelines through a broad spectrum of technology access arrangements.
As a profitable privately-held biotech company, we take a long-term view on value creation and make substantial investments in technology development, research, and our people. We offer individually tailored compensation packages comprised of a competitive salary, meaningful equity, a 2:1 401(k) match, and comprehensive health care benefits.
Located in New Hampshire’s beautiful Upper Connecticut River Valley, we are minutes from Dartmouth College, the Geisel School of Medicine, the Thayer School of Engineering, the Tuck School of Business, and the Dartmouth Hitchcock Medical Center. We are fortunate to be situated in an area that is renowned for its premier skiing, hiking, kayaking, and biking.
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DXNnB27kEy

Research Associate, Antibody & Protein Engineering

<h3>Job Description</h3>
Job DescriptionWho We Are
TetraScience is the Scientific Data and AI company. We are catalyzing the Scientific AI revolution by designing and industrializing AI-native scientific data sets, which we bring to life in a growing suite of next gen lab data management solutions, scientific use cases, and AI-enabled outcomes. 
TetraScience is the category leader in this vital new market, generating more revenue than all other companies in the aggregate. In the last year alone, the world’s dominant players in compute, cloud, data, and AI infrastructure have converged on TetraScience as the de facto standard, entering into co-innovation and go-to-market partnerships: Latest News and Announcements | TetraScience Newsroom: 
In connection with your candidacy, you will be asked to carefully review the Tetra Way letter, authored directly by Patrick Grady, our co-founder and CEO. This letter is designed to assist you in better understanding whether TetraScience is the right fit for you from a values and ethos perspective. 
It is impossible to overstate the importance of this document and you are encouraged to take it literally and reflect on whether you are aligned with our unique approach to company and team building. If you join us, you will be expected to embody its contents each day. 
Who You Are
You are a strategic, analytically minded professional with a passion for bridging scientific insights and cutting-edge technology. You thrive in environments where you can collaborate with scientists, product managers, and engineers to transform complex scientific data into actionable outcomes.
With deep domain knowledge in drug discovery/preclinical development, CMC, or Quality, you are skilled at uncovering innovative use cases that drive AI and machine learning applications. Your ability to engage with scientists and business leaders alike makes you a key player in maximizing the value of scientific data.
You will need to be a high clock speed and forward-thinking individual with a passion for developing requirements for complex solutions targeted to R&amp;D and Quality personas inside of Life Sciences. 
You will need to be a high clock-speed, forward-thinking individual with a passion for developing requirements for complex solutions targeted to R&amp;D and Quality personas inside Life Sciences. You embody extreme ownership and have a demonstrated history of deriving maximum value from data through enrichment, analysis, and integration with AI and machine learning applications.
You should also be energized by regularly working onsite with customers. You thrive in dynamic, high-impact, face-to-face collaborative environments where you can build deep relationships and drive scientific transformation firsthand.
Requirements
What You Have Done
<ul>
<li>PhD with 15+ years of industry experience in life sciences, preferably across pharma, biotech, or health tech, with deep domain expertise in discovery, preclinical, CMC, and/or Quality.</li>
<li>Extensive hands-on experience or direct oversight in one or more of the following areas: high throughput screening, preclinical toxicology, materials engineering, analytical development, drug substance (DS) synthesis and manufacturing.</li>
<li>Delivered requirements for AI/ML-driven solutions in operational or productized environments that improved efficiency, reduced cost, and enhanced data utilization.</li>
<li>Extensive hands-on experience with scientific data workflows and lab automation; exposure to FAIR principles and modern data architecture is a plus.</li>
<li>Strong coding or scripting background (e.g., Python, Nextflow, AWS, SDKs) and familiarity with scientific tools, databases, and ontologies is preferred.</li>
<li>Exceptional communication and storytelling ability to engage technical and executive stakeholders.</li>
<li>Prior experience in customer-facing, consulting, or commercial-scientific interface roles.</li>
</ul>
What You Will Do
<ul>
<li>You will be a critical team member in a unique partnership to industrialize Scientific AI. As such, you will engage directly with customers onsite up to 4-5 days per week in the Boston Region</li>
<li>Customer Data Exploration: Investigate diverse customer datasets, identifying enrichment and AI-readiness opportunities.</li>
<li>Scientific Use Case Development: Collaborate with customers to define, iterate, and implement innovative scientific AI/ML use cases.</li>
<li>Stakeholder Engagement: Conduct onsite interviews and workshops to deeply understand customer challenges and data landscapes.</li>
<li>Data Analysis and Enrichment: Perform exploratory data analysis and define transformation workflows that enable scientific AI.</li>
<li>Workflow Documentation: Develop visual documentation including workflow diagrams, ERDs, and ontology definitions.</li>
<li>AI Model Evaluation: Provide practical scientific input on model output, with suggestions to improve real-world performance.</li>
<li>Customer Enablement: Deliver onsite demonstrations, conduct working sessions, and act as a trusted advisor in AI adoption.</li>
<li>Strategic Insight: Propose new directions, experiments, or platforms that can amplify scientific discovery and development.</li>
</ul>
Benefits
<ul>
<li>100% employer-paid benefits for all eligible employees and immediate family members</li>
<li>Unlimited paid time off (PTO)</li>
<li>401K</li>
<li>Remote working opportunities, when not at customer sites </li>
<li>Company paid Life Insurance, LTD/STD</li>
<li>A culture of continuous improvement where you can grow your career and get coaching</li>
</ul>

Scientific Business Analyst, Scientific AI- Boston

<h3>Job Description</h3>
Job Description
Discover Veranova
At Veranova, we believe people are our most important asset, and we are dedicated to building the most talented workforce in our industry. Our commitment to uncompromising focuses on quality, compliance, safety, and excellence in delivery shapes everything we do. We are not just looking for skills; we are seeking innovative individuals who have a mindset open to learning and growth, and a desire to make a difference.
Veranova is a global leader in the development and manufacturing of complex active pharmaceutical ingredients (APIs) for pharma and biotech customers. With deep technical expertise and impressive flexibility, we develop solutions and processes that support and accelerate innovation. 
Join us on our mission to enable current and next-generation therapeutics to improve and save the lives of patients. 
Role Overview:
The Analytical/QC Lab Metrologist is responsible for the timely installation, maintenance, repair, calibration, and IQ/OQ of instruments, balances, and other equipment used by the Analytical Development (AD) and Quality Control (QC) groups. This role also ensures Standard Operating Procedures are technically sound and provide full regulatory compliance. This position is critical to supporting high-quality science, operational excellence, and regulatory compliance across both sites.
Core Responsibilities: 
<ul>
<li>Revises and reviews metrology-related protocols and IQ/OQ to ascertain proper functioning of the instrumentation. Ensures that appropriate documentation for the instrument calibration program is in place for compliance with regulatory expectations.</li>
<li>Schedules, executes and supports instrument calibrations and preventative maintenance in such a way so as not disrupt the analysts using the instruments. Responsible in the assignment of instrument custodians, assuring instrument maintenance and usage logbooks have been maintained. Trouble shooting or judging the issue for chromatographic systems mainly LC/GC.</li>
<li>Negotiates and manages contracts with external vendors and contracted services as required. Oversees the work of contracted personnel to install/modify equipment and systems in accordance with the specific needs of the AD and QC groups while meeting all cGMP and USP requirements.</li>
<li>Keep abreast of instrument validation requirements to ensure compliance with respect to USP and cGMP requirements.</li>
<li>Provides assistance in internal and customer audits by providing relevant, up to date documentation related to calibration, qualification and maintenance of appropriate analytical instrumentation used by the analytical groups. </li>
<li>Leads the process to evaluate, purchase and install new instrumentation. Interacts with internal and external vendors to ensure the proper instrumentation is identified to support the needs of the business. Evaluates and recommends appropriate application of new software packages as well as upgrades of software/firmware/hardware.</li>
<li>Directly involved with and supports investigations that are instrument related. Conducts all work in compliance with USP and cGMP standards and all other appropriate Federal, state and local regulations.</li>
</ul>
Qualifications: 
Required
<ul>
<li>Bachelor’s Degree in chemistry or a related science with a minimum of 5 years’ related experience </li>
<li>Familiarity with LC/GC trouble shooting.</li>
<li>Experience in a cGMP environment</li>
<li>Ability to exercise independent judgment in the application of scientific principles pertaining to analyses as related to this business and operation </li>
<li>Proficiency with computers and other software packages relevant to installation, modification, calibration and qualification of instrumentation systems and equipment</li>
<li>Strong communication skills; written and verbal. </li>
<li>Possess strong organizational skills</li>
</ul>
Preferred
<ul>
<li>Experience in lab equipment such as analytical balance, micro balance, KF, OVEN-KF, NMR, ICP-MS, PSD, XRPD, TGA, DSC, etc. </li>
<li>Experience or familiarity with Labware LIMS and the Instrument Manager module</li>
<li>Experience or familiarity with Master Control and Veeva</li>
<li>Recent relevant experience in bulk pharmaceutical/API manufacturing or specialty chemicals</li>
</ul>
Salary Range: $90,000 - $105,000 annual base salary
Our Commitment:
<ul>
<li>Health &amp; Wellness: Comprehensive health &amp; Wellness benefits. Access to mental health resources and wellness programs. Generous PTO and holiday pay policies. </li>
<li>Financial Wellness: Veranova is committed to fair and transparent compensation practices. This includes a competitive base salary, eligibility for performance-based bonuses, and an attractive 401(k) Plan with company match. Salary ranges reflect the scope and expectations of the role, and are based on market data, internal equity, and role-specific factors. Final compensation may vary depending on experience, skills, education, and business needs.</li>
<li>Professional Development: Opportunities for continuous learning through LinkedIn Learning, workshops, conferences, and mentorship. Tuition Assistance for Undergraduate and Graduate degree programs.</li>
<li>Inclusive Culture: At Veranova, an inclusive culture is integral to our values. We are committed to ensuring that everyone can bring their full self to work and thrive in their career.</li>
</ul>
How to Apply: 
At Veranova, we are on a mission to meet people that believe in our values and can contribute to the team in a variety of ways. Please visit <a href="http://www.veranova.com" target="_blank">www.veranova.com</a> to view all open roles and join our Talent Community to stay connected and learn about opportunities as they arise. 
We value a range of experiences and perspectives. If you want to be part of improving and saving the lives of patients, we encourage you to apply regardless of whether you meet every qualification listed. 
Additional Information:
Applicants for this role must be authorized to work in the United States without further employer sponsorship. 
Agency and Search Firm Representatives: Veranova does not accept unsolicited resumes from agencies and/or search firms for this job posting. 
All your information will be kept confidential according to EEO guidelines.
Veranova is an Equal Opportunity Employer. It is the policy of Veranova to provide equal employment access and opportunity to all persons regardless of age, race, color, national origin, religion, sex, sexual orientation, gender identity and/or expression, physical or mental disability, genetic information, citizenship, marital status, veteran status, or any other characteristic protected by federal, state, or local law.
All applications are carefully considered, and your details will be stored on our secure Application Management System. This is used throughout Veranova for the selection of suitable candidates for our vacancies as they arise. Veranova respects your privacy and is committed to protecting your personal information. For more information about how your personal data is used please view our privacy notice.
#LI-Onsite

Analytical/Quality Control Lab Metrologist

<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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