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<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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Research Associate, Antibody & Protein Engineering

<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.

Qc Lab Analyst

<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.

<h3>Job Description</h3>
Job Description
Description:
<ul>
<li>
This position is in the Biologics Purification Development team of the Product Development Science and Technology department at Bioresearch Center.
</li>
<li>
The candidate will be involved with all aspects of protein purification and protein chemistry to support biopharmaceutical process development.
</li>
<li>
Execute high through put scale down robotic purification as part of early and late stage process development, viral clearance, process characterization, and continuous process improvement studies.
</li>
<li>
Perform basic data acquisition and analysis, and documentation in electric lab notebooks.
</li>
<li>
Will develop economical, robust steps for recovering the target protein from bioreactor harvests using chromatography, filtration, and other separation techniques; developing downstream purification processes to be transferred to manufacturing; and perform laboratory scale process characterization studies.
</li>
<li>
Perform various bioanalytical assays, including HPLC, ELISAs and SDS-PAGE, to aid in rapid process development.
</li>
<li>
As appropriate, the candidate may supply technical support for pilot and/or GMP manufacturing of clinical materials.
</li>
</ul>
Qualifications:
<ul>
<li>
BS in Chemical Engineering, Biochemistry, or Chemistry with 3-5 years experience; OR
</li>
<li>
Master's Degree with 2 years' experience 
</li>
<li>
Strong biological scientific understanding.
</li>
<li>
Experience with chromatography and filtration for biologics purification
</li>
<li>
Experience with bioanalytical assays and methods preferred
</li>
<li>
Strong written, oral, and collaborative skills in order to effectively communicate experimental procedures and results.
</li>
<li>
Experience with Lab work particularly with process development
</li>
<li>
Small scale Chromatography, high throughput, AKTA is a huge plus 
</li>
</ul>
Benefits:
Healthcare Insurance: Synectics offers eligible employees and their dependents healthcare coverage through BlueCross BlueShield of Illinois. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. Premiums are subsidized by Synectics. 
Dental Insurance: Synectics offers eligible employees and their dependents a dental plan through MetLife. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. 
Vision Insurance: Synectics offers eligible employees vision insurance through VSP. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics.401(k) Plan: The Synectics Inc. Investment Savings Retirement Plan. Synectics offers all employees who are 21 years of age or older the opportunity to invest in the 401(k) Plan on the first enrollment date that is at least 30 days after employment begins. Enrollment dates are each January 1st, April 1st, July 1st, and October 1st.
Technical Certification Bonus: Synectics is pleased to award its employees a bonus of up to $500 for an approved professional certification. In determining the bonus amount, Synectics will consider the cost of the test(s) for any certification relating to your current position, achieved during your employment with us. Only one Certification Bonus per calendar year may be awarded per employee. Only current, active employees will be eligible to receive this bonus. It will be awarded 90 days after the Synectics office has received documentation confirming the successful completion of the certification.
Synectics is an equal opportunity employer.

Biologist

<h3>Job Description</h3>
Job Description
Production Technician – Biotechnology
We’re seeking a detail-oriented and safety-conscious Production Technician to join our biotechnology team. In this role, you’ll be responsible for executing defined production procedures in a GMP-regulated environment, supporting manufacturing operations, and maintaining a clean, organized, and safe workspace.
Responsibilities:
<ul>
<li>Perform production tasks according to established schedules and procedures.</li>
<li>Ensure compliance with company policies and cGMP regulations.</li>
<li>Maintain a safe work environment and actively participate in site safety initiatives.</li>
<li>Execute lab start-up and shutdown procedures.</li>
<li>Keep work areas clean and well-stocked with necessary supplies.</li>
<li>Operate and monitor equipment including spectrophotometers, pH meters, and automated systems.</li>
<li>Perform routine tasks such as buffer preparation, pH testing, UV measurements, and fraction collection.</li>
<li>Support synthesis and purification processes, including equipment cleaning, solution prep, and column packing.</li>
</ul>
Qualifications:
<ul>
<li>Biotechnology certificate or college degree preferred.</li>
<li>2–5 years of experience in a GMP-regulated environment.</li>
<li>Hands-on experience with pH testing, aseptic technique, buffer preparation, and chromatography.</li>
<li>Strong attention to detail and ability to follow SOPs and safety protocols.</li>
</ul>
Top Skills:
<ul>
<li>pH testing</li>
<li>Aseptic technique</li>
<li>Buffer preparation</li>
</ul>
If interested, please reach out to directly to Lindsee Allienello at lallienello @ actalentservices.com. 
Pay and Benefits
The pay range for this position is $30.00 - $31.25/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 Milford,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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