Chemist jobs in Lawrence, MA - 313 jobs

Sr. QC Analyst, Flow Cytometry & Molecular Team, will be executing analytical method transfers to Quality Control, optimize and troubleshoot assays for improvement. He/she will be responsible for authoring protocols, authoring Standard Operating Procedures (SOPs) and Test Methods. He/she will be executing various quality control methods, analyzing data, and reporting data. He/she will assist in the implementation of new assay methodologies and the associated instrumentation. Identifies and supports initiation and completion of deviations, corrective and preventative actions, and laboratory investigations in compliance with all applicable quality systems and current cGMPs. This position is highly visible in the organization and requires the ability to interface with multiple groups, and the ability to assess method suitability, interpret results, perform tasks independently, and troubleshoot. HOW YOU WILL MAKE AN IMPACT Perform routine and non-routine quality control testing on in-process samples and finished products. Operate and maintain laboratory equipment and instruments, ensuring proper calibration and adherence to cGMP Compliance. Provide support for method feasibility/transfers/qualification/validation and stability testing. Support analytical equipment installation and qualification Apply technical knowledge and abilities to ensure all testing is performed in a compliant manner. Review all data in accordance with applicable procedures and cGMP requirements. Author, review, and/or approve Protocols, SOPs, Test Methods, and other procedures required to operate a QC laboratory. Participate in internal and external audits, inspections, investigations, change controls and CAPAs Contribute to continuous improvement initiatives, identifying opportunities for efficiency gains and process optimization within the quality control function. Anticipate and troubleshoot problems. Communicate effectively with management regarding task completion, roadblocks, and needs. Become a qualified trainer on assigned assays and deliver training to analysts, documenting training per procedural and cGMP requirements. Provide support to QC Analytical Subject Matter Expert in Flow Cytometry. Work independently in a high-paced team environment, meet deadlines, and prioritize work from multiple projects. Communicate effectively with cross-functional peers, and department management. WHAT YOU WILL BRING Bachelor's Degree in scientific discipline. 4+ years of relevant experience in cGMP Quality Control Laboratory. Hands-on experience with various analytical techniques such as flow cytometry, qPCR, dPCR, ELISAs,cell-based assays, and scientific knowledge in the characterization and transfer of analytical methods. Experience with rapid microbiological methods is a plus (e.g. mycoplasma) Knowledge of cGMP/ICH/FDA regulations. Ability to independently prioritize/manage activities. Ability to prioritize objectives from multiple projects and adhere to scheduled timelines while maintaining flexibility and attention to detail. Proficient in MS Office applications and information technologies that support documentation and data management systems. Strong troubleshooting, problem-solving skills, oral and written skills. Ability to multi-task and interact with multiple groups in a team-oriented environment.

Vicor is seeking a Wet Chemistry Lab Technician to join 3rd shift operations Sunday - Thursday. This individual will work in the wet chemistry process lab to support all plating fabrication operations. The candidate will work with the wet chemistry lab team for day to day production analysis as well as special projects. Job Description * Perform basic chemical analysis techniques. * Utilize chemical analysis equipment to include Auto-Titration, CVS, ICP, and UV-VIS. * Ability to input analysis results into TrueChem. * Maintain lab safety policies and procedures. Education / Qualifications * 1+ years of prior laboratory experience required. * Experience with Titration analysis, ICP or AA, UV-VIS. * Knowledge of operation and maintenance of lab equipment highly desired. * Knowledge of Microsoft Word, Excel, and PowerPoint required. * Must pay high attention to detail, possess self-motivating skills, and have the ability to self-inspect for quality and accuracy. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability or protected veteran status. Vicor is an EO employer - M/F/Veteran/Disability Compensation Data Salary Range: $22 - $25/hour Please note: This range is based on our current market driven pay structures. Individual salaries are determined based upon a variety of factors including but not limited to, a candidates overall qualifications, such as skills, education, and experience as well as company internal equity.

IRI believes in commitment, integrity and strategic workforce solutions. Integrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce solutions that help you manage your talent and business more efficiently and effectively. Since launching in 1996, IRI has attracted, assembled and retained key employees who are experts in their fields. This has helped us expand into new sectors and steadily grow. We've stayed true to our focus of finding qualified and experienced professionals in our specialty areas. Our partner-employers know that they can rely on us to find the right match between their needs and the abilities of our top-tier candidates. By continually exceeding their expectations, we have built successful ongoing partnerships that help us stay true to our commitments of performance and integrity. Our team works hard to deliver a tailored approach for each and every client, critical in matching the right employers with the right candidates. We forge partnerships that are meant for the long term and align skills and cultures. At IRI, we know that our success is directly tied to our clients' success. Job Description • A position is available for a highly skilled analytical chemist or engineer to join in Pharmacokinetics Dynamics and Metabolism New Biological Entities (PDM-NBE) ADME group with deep expertise in antibody ADME and inter-molecular binding • The lab based role entails training on the state-of-the-art technology for intermolecular interactions and quantification of binding affinity of Biotherapeutics drug to specific proteins in human biological matrices with unwanted immunogenicity • This position requires strong analytical expertise, with background in engineering, protein biochemistry, immunology or PK as a plus • The candidate will participate in all phases of laboratory operations including training on the technology, design of reagents, design of binding experiments, the development of sample preparation, assay execution, instrument maintenance, data analysis, summarization and reporting • We are looking for a scientist passionate about learning and able to quickly apply new skills to the project needs. Responsibilities- • Design of protein reagents to be used in binding studies • Run binding assays under minimal supervision; initiative in method development is expected • Independent daily operation, calibration, maintenance, and troubleshooting the binding instrument • Analysis of binding data and derive binding affinity using relevant software • Work with modeller to build computational immunogenicity model • Handling of biological samples, specifically human and preclinical serum and tissues • Summarize work and write reports Qualifications • BS/MS level education in Analytical Sciences, Biochemistry, Chemistry, Pharmacology or closely related fields required; advanced degree may be a plus • Industry experience in biopharma preferred • Attention to detail is critical, and be able to handle very delicate and complicated instrument to produce reproducible data • Strong analytical and biochemistry background is required. Good understanding of concepts of binding affinities is a plus • Fast learner and be able to master running/maintaining the instrument after a short period of training • Strong initiative for problem solving at a technical and intellectual level • Excellent communication skills, both written and oral • Works well both independently and as part of a team • Collaborative skills and effective partnering skills in a matrix-environment • Strong data organization and analysis skills Additional Information Thanks Regards Ricky

About Us Eat Well, Live Well. At Ajinomoto Cambrooke, we build careers grounded in helping improve people's health through nutritional therapies. Ajinomoto Cambrooke (ACI) was founded by parents looking to develop better solutions for their children with PKU. Over the subsequent 25 years, we have expanded into additional therapeutic areas with a focus on enjoyable nutrition as a core part of normalizing the life for people living with medical conditions. Joining ACI means becoming part of a diverse team of talented people who want to build their careers while contributing back to society in a positive way. We seek individuals who bring an entrepreneurial mindset with a bias for action and finding solutions. We provide an environment based in mutual respect and collaboration to support you and give you opportunities to learn and develop. Join us to find a rewarding work experience that lets you be at your best and have an impact on our patient communities. Why Join Us Our people are the key ingredient to our success. We offer a collaborative, innovative environment where you can grow your career and make an impact on global food and health solutions. We provide a comprehensive and competitive total rewards package, including: • Competitive Pay and Annual Bonus Opportunity • 401(k) with Company Contributions • Medical, Dental, and Vision - Effective Day 1 • Paid Time Off, Company Holidays, and Floating Holidays • Paid Parental Leave • Wellness Programs and Yearly Wellness Reimbursement • Work Flexibility • Company-Paid Life and Disability Insurance • Employee Assistance Program (EAP) • Tuition Reimbursement Opportunities • Career Growth and Development within a Global Organization • Company-Provided Mental Health and Caregiving support Overview The Product Development Team supports the medical nutrition business by developing new and revising existing product formulations to meet target characteristics that will deliver positive patient outcomes through therapeutic nutrition. Strong collaboration with the Directors of Medical Nutrition, Marketing, and Sales will be required to ensure desired nutritional levels are achieved throughout the product shelf-life, patient insights on flavor, texture, and palatability are incorporated. In this role, you will contribute to the ideation and exploration for uses of new to ACI ingredients and new to ACI business ventures in additional disease-states reliant on specialized medical nutrition. This position sits in our Corporate Office located in Ayer, MA. Qualifications EDUCATION, CERTIFICATIONS AND EXPERIENCE: • Minimum bachelor's in food science, nutrition, or related field; Master's degree preferred. PhD, PharmD a plus. • 5+ years of experience in product development, with ability to take concepts from bench top to commercialization for nutritional beverages and / or nutritional powder blends from concept to commercialization. • 5+ years in basic and applied research and development preferably in small/mid-sized nutrition, food and/or biotech company. Experience with food/beverage formulation and manufacture of nutritional products that meet stability, sensory and nutritional requirements. Direct experience with aseptic processing / Tetra Pak a plus. • Expert scientific knowledge in food science with emphasis on product development involving interaction amongst ingredients and impact of process techniques on use of micro-nutrients. • Experience with nutritional modeling software and familiarity with FDA regulations preferred, exposure to EU regulations a plus. • Able to design and monitor product shelf-life procedures both regular and accelerated for nutritional products. • Strong translational science background with experience in converting basic nutrition-science insights into consumable products. KNOWLEDGE, SKILLS AND ABILITIES: • Build relationships with vendors to source ingredients to meet product specifications. • Overall understanding of how business units interact to facilitate successful product development and commercialization. • Ability to define new product needs in terms of process needs and product characteristics including organoleptic needs / claims • Demonstrated Leadership capability with a focus on innovation to drive product development proactively and passionately. • Exhibit the understanding of use of standard operation procedures related to product development, process development and product shelf-life determination. • Well versed with food safety requirements and regulations. • An understanding of human nutrition and ability to review primary scientific literature. • A strong ability to communicate basic science and technical challenges to non-technical audiences. • A strong understanding of ingredient interactions in a food/beverage matrix throughout processing and shelf life. • Ability to design shelf-life evaluation matrices considering product composition, process impact and other critical factors when designing new products in medical nutrition arena. • An understanding of macro and micro-nutrient analytical procedures and their principles. • Ability to work in a fast paced, cross functional team environment. • Excellent analytical skills, strong attention to details, good communication and interpersonal skills. • Excellent organizational skills, the ability to balance multiple projects, set priorities, and drive results. Working Conditions / Physical Requirements WORKING CONDITIONS: This position works in a food manufacturing environment and requires the ability to adhere to all GMP, Food Safety, workplace safety and security policies including wearing required personal protective equipment, as well hair net, beard net, etc. as required PHYSICAL REQUIREMENTS: Position requires the ability to occasionally lift up to 50 pounds, stand, walk, bend, reach, push, and pull. Ability to use a computer, keyboard, telephone, and other office equipment. Ability to wear all required PPE. Responsibilities • Utilize your exemplary food science and ingredient know-how to co-create and execute medical formula products against ACI's strategic R&D roadmap to support the overall corporate strategy while meeting the internal quality expectations. • Support the Leadership and Management teams with scientific support in the areas of product development, clinical development, product manufacturing and new ingredient compound / product initiatives. • Research and help develop clinical evidence supporting existing and new products and ingredient compounds for use in commercial activities. • Participate in conferences, clinician meetings and other forums to present ACI's clinical evidence. • Ensure existing and new products, processes or ingredient compounds have strong Intellectual Property protection thus providing ACI a sustained competitive advantage. • Other duties as assigned. Salary Range $105,000 - $130,000 Annual with potential 12.5% Bonus EEO Statement Ajinomoto Cambrooke, Inc. is an Equal Opportunity Employer-Vets/Disabled, committed to a diverse workforce. If you need assistance with completion of an application for employment, please contact Human Resources Department at ************.

Title: Analytical Chemist Contract Term: 12+ Months Shift/Hours: 1st Shift ( 8-9am to 4-5pm) / 40hrs Client: Medical Device Company Job Category: Research & Development Employment Type: Contract on W2 (Need US Citizens Or GC Holders Only) No H1B's Summary: The Analytical Chemist will work in a R&D laboratory to support chemical testing using chromatography and spectroscopy. Responsibilities • Conduct basic and complex analyses of raw material and or/stability samples chemical analytical techniques • Effectively document and communicate test results • Set up and operate laboratory equipment such UV, HPLC and Fluorometer including any computerized software required for the operation of the equipment or analysis of results. • Make recommendations with respect to the cause and resolution of equipment issues or malfunction • Co-ordinate and prioritize sample analysis in consultation with other laboratory personnel • Conduct investigations of laboratory incidents and the investigation of out-of-specification and out-of-trend results. • Document investigations in a clear, accurate and concise fashion. • Review the work for accuracy and completeness. • Perform routine maintenance activities in the laboratory and participates in the qualification and periodic calibration of equipment. • Participate in method transfer studies and in other laboratory testing to support compliance (e.g. testing of product validation samples). • Write protocols and execute analytical method validations. • Develop and execute testing protocols. • Support exploratory testing to define test equipment, test fixtures and test methods development. • Participate in training, test methods validation, and execution of testing as needed • Write engineering test reports and final test reports • Install and validate equipment and or test fixtures as needed, manage and maintain laboratory equipment and inventory • Support failure analysis Requirements: • Minimum of Bachelor's Degree in Chemistry • Industrial experience in the use of HPLC and/or UPLC. • Knowledge of Microsoft Office programs (Word, Excel, PowerPoint) is a must • Ability to understand and execute test procedures • Demonstrated attention to details and very organized

Job DescriptionProduct Development Scientist - Medical Nutrition Industry: Food Production / Medical Nutrition Experience: Mid-Level (5+ years) Education: Bachelor's degree required Positions: 1 Relocation: Limited assistance available Visa Sponsorship: Not available Overview Seeking a Product Development Scientist to develop and optimize medical nutrition beverage and powder formulations in a manufacturing environment. This role supports product innovation, ingredient initiatives, clinical evidence development, and compliance with GMP and food safety standards. Responsibilities Develop and optimize nutritional beverage and powder formulations Conduct bench-level formulation, testing, and troubleshooting Execute shelf-life and stability studies Research and evaluate new ingredients Support scale-up, manufacturing, and commercialization activities Collaborate with cross-functional teams (R&D, Quality, Manufacturing, Commercial) Ensure compliance with GMP and food safety requirements Support documentation and IP protection efforts Additional Info On-site role in Ayer, MA Limited relocation assistance available No visa sponsorship available JD Summary:Develop and optimize medical nutrition beverage and powder formulations; apply food science and ingredient expertise; collaborate with Medical Nutrition, Marketing, Sales, Manufacturing; research new ingredients; support clinical evidence development; manage ingredient vendors; support IP protection; ensure GMP, food safety, and workplace safety compliance; participate in conferences and clinician meetings; support manufacturing and new product initiatives. RequirementsRequirements Bachelor's degree in Food Science, Nutrition, or related field (Master's preferred) 5+ years of product development experience in food, beverage, medical nutrition, supplement, or nutraceuticals Strong knowledge of ingredient functionality and nutrient stability Experience with GMPs and FDA food regulations Hands-on lab and pilot-scale experience required PLM or formulation software experience preferred

Our client is seeking a Product Development Scientist to develop and optimize medical nutrition beverages and powder formulations that support patient outcomes and clinical evidence. This role combines hands‑on bench formulation, ingredient research, stability testing, and cross‑functional collaboration across R&D, Clinical, Manufacturing, and Marketing. You will play a key role in advancing the company's medical nutrition portfolio, supporting new product innovation, ingredient initiatives, and regulatory compliance. Onsite | No Visa Sponsorship | Relocation Assistance: Limited Responsibilities: Formulation & Product Development Execute sensory, stability, and shelf‑life studies. Develop and optimize medical nutrition beverages and powders. Conduct bench‑level formulation, testing, and troubleshooting. Evaluate ingredient functionality, nutrient stability, and processing impact. Cross‑Functional Collaboration Partner with Medical Nutrition, Marketing, Sales, and Clinical teams. Support clinical evidence development for new and existing products. Present scientific findings at conferences and clinician meetings. Ingredient & Vendor Management Research new ingredients and medical nutrition opportunities. Manage vendor relationships and source compliant ingredients. Regulatory, Quality & Compliance Ensure adherence to GMP, food safety, and FDA regulations. Support IP protection for formulations, processes, and ingredients. Additional Responsibilities Perform other duties as assigned. Provide scientific support across R&D and manufacturing. Participate in pilot plant trials and scale‑up activities. Qualifications/Must Haves: Familiarity with GMPs and FDA regulations. Experience conducting shelf‑life and stability studies. Proven bench‑level formulation and troubleshooting experience. Strong understanding of ingredient functionality and nutrient stability. Bachelor's degree in Food Science, Nutrition, or related field (Masters preferred; PhD/PharmD a plus) 5+ years of hands‑on product development experience in food, beverage, nutrition, supplement, or nutraceutical industries. Preferred Skills: Exposure to EU regulatory frameworks. Experience with PLM systems and nutritional formulation tools. Experience with aseptic processing or medical nutrition products. Experience in small to mid‑sized food or medical nutrition companies.

Mindlance is a national recruiting company which partners with many of the leading employers across the country. Feel free to check us out at ************************* Qualifications Compendial testing Additional Information If you or anyone from your connections is looking for a change; do call me on ************ or send me updated resume on gurupreet@mindlance(dot)com

About the Role The Small-Scale Cell Culture Scientist is a hands-on technical contributor in the Bioprocess Design Center (BDC), responsible for designing, executing, and documenting upstream cell culture experiments that generate high-quality technical evidence for Thermo Fisher Scientific's single-use bioprocessing technologies. This role operates at the intersection of experimental biology and systems-level process design. The successful candidate will independently own small-scale cell culture studies, translate experimental outcomes into actionable insights, and support integrated workflow development across upstream unit operations. While primarily lab-focused, the role requires strong communication skills and comfort engaging with cross-functional partners and customers. Location: This is an onsite position in Plainville, Massachusetts. Residency within commuting distance is required. No relocation assistance will be provided. Key Responsibilities Experimental Design & Execution Independently design and execute small-scale upstream cell culture experiments (typically 2L-50L) using single-use bioreactor systems. Incorporate process analytical techniques (PAT), online sensors, and at-line/off-line analytics to monitor and assess cell culture performance. Execute mammalian cell culture processes such as fed-batch and intensified workflows, ensuring reproducibility, data integrity, and traceability. Troubleshoot experimental and data-related issues, including sensor performance, data quality, and process variability. Systems, Automation & PAT enablement Analyze experimental datasets using advanced data analytics approaches, including multivariate analysis, trend analysis, and statistical methods, as appropriate. Leverage JUMP™ and other analytical programs to support data-driven decision making and improve experimental efficiency. Translate complex datasets into clear, defensible conclusions and visual summaries suitable for internal and customer-facing audiences. Author protocols, technical reports, summaries, and SOPs that integrate experimental outcomes with process data insights. Data Analysis & Digital Enablement Analyze experimental datasets using advanced data analytics approaches, including multivariate analysis, trend analysis, and statistical methods, as appropriate. Leverage JUMP™ and other analytical programs to support data-driven decision making and improve experimental efficiency. Translate complex datasets into clear, defensible conclusions and visual summaries suitable for internal and customer-facing audiences. Author protocols, technical reports, summaries, and SOPs that integrate experimental outcomes with process data insights. Collaboration & Communication Collaborate closely with engineers, scientists, and cross-functional teams to align experimental work with BDC priorities. Support customer visits, technical demonstrations, and internal reviews by clearly explaining experimental intent and results. Communicate progress, risks, and outcomes effectively to technical and non-technical audiences. Laboratory Operations & Compliance Maintain a safe, compliant, and organized laboratory environment. Follow applicable safety, quality, and data integrity requirements. Contribute to continuous improvement of lab workflows and experimental practices. Qualifications Education B.S. in Chemical Engineering, Biochemical Engineering, Biotechnology, Bioengineering, or a related field with 3+ years of relevant experience M.S. with 2+ years of relevant experience Equivalent combinations of education and experience will be considered Experience & Skills Hands-on experience with mammalian cell culture and upstream bioprocessing Familiarity with single-use bioreactor systems and small-scale process development Experience designing and executing controlled experiments; DOE experience preferred Strong data analysis, documentation, and technical writing skills Working knowledge of GLP/GMP concepts and laboratory best practices Proficiency with standard data analysis and reporting tools (e.g., Excel, PowerPoint) Preferred Attributes Demonstrated ability to work independently in a fast-paced, matrixed environment Strong problem-solving skills and attention to detail Ability to translate experimental data into practical insights Comfortable operating in environments with evolving requirements and priorities Collaborative mindset with a customer-centric orientation Physical Requirements Ability to work in a laboratory environment and handle light to moderate lifting (up to ~50 lbs) Standing and walking for extended periods during experimental execution Manual dexterity to operate laboratory equipment and instrumentation Why Join the Bioprocess Design Center The BDC is where Thermo Fisher technologies are stress-tested, validated, and transformed into real-world solutions for our customers. This role offers the opportunity to work hands-on with cutting-edge single-use systems, contribute to evidence that shapes customer confidence, and grow within a technically rigorous, highly collaborative environment. Compensation and Benefits The salary range estimated for this position based in Massachusetts is $96,000.00-$127,000.00. This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes: A choice of national medical and dental plans, and a national vision plan, including health incentive programs Employee assistance and family support programs, including commuter benefits and tuition reimbursement At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan Employees' Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount For more information on our benefits, please visit: *****************************************************

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! Job Description We are seeking a candidate that will support a client team that is responsible for developing robust and efficient purification processes of recombinant proteins and other biological therapeutics from early to late stage of development. We are seeking an analytical scientist who will work in a collaborative environment to be engaged in the analysis, monitoring and characterization of in-process samples to support the client in improving process performance by optimizing product recovery and impurity removal. This role will provide routine analytical testing. Knowledge and expertise in analytical biochemical techniques including HPLC (HI-C, RP, SEC, etc.), and Octet are a must. The successful candidate must be self-motivated and able to work independently, be accountable for own results and prioritize own workflow, and seek opportunities to take on new projects. Job Responsibilities and Requirements: Experience with protein chemistry, protein analytics, and bioprocess technology is required Expertise in analytical chemistry using a broad range of separation, chromatographic, spectroscopic and other detection techniques to characterize and monitor protein purification process Hands on experience and working knowledge on techniques including but not limited to liquid chromatography like UPLC/HPLC (size-exclusion, hydrophobic, ion-exchange, affinity), and Octet Hands on experience with SDS-PAGE, ELISA, and experience with protein purification/chromatography at the lab scale is a plus A working knowledge on Empower and/or ChemStation control and data analysis software is strongly preferred Work closely with colleagues by providing quality data to support product development through early clinical phases in a timely manner; uses understanding of analytical tools to assess and interpret experimental data Maintains written records (electronic lab notebooks and databases) of all experimental work in accordance with Good Laboratory Practices Leads in the routine calibration, maintenance, troubleshooting and repair of laboratory instruments, systems or apparatus and may interact with internal site or external vendors in the maintenance and continuous improvement of safe and effective working practices Qualifications Bachelors or Masters Degree in Biotechnology, Biochemical Engineering, Analytical Chemistry, Chemical Engineering or other related discipline BS 2-4 years or MS +0-2 years of relevant experience Experience with HPLC (SEC, HIC, and RP), protein purification methods, and octet Excellent attention to detail and ability to follow procedures to generate reproducible data in a controlled laboratory environment Excellent skills in Microsoft Office, data analysis software, and other related applications Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies Ability to think critically and demonstrate troubleshooting/problem solving skills Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude Authorization to work in the United States indefinitely without restriction or sponsorship Additional Information The position is full-time, on-site, Monday through Friday, 8:00 AM-5:00 PM. Pay range: $27.00 - $31.00 based on degree level and years of relevant experience Excellent full-time benefits including: Comprehensive medical coverage, dental, and vision options Life and disability insurance 401(k) with company match Paid vacation and holidays Ready to take the next step in your career? Apply today and join a team that's making a difference in science every day. Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Job Description InnoTECH Staffing is looking to hire a fulltime permanent Coatings Lab Technician for a materials development company just North of Boston, MA. This is an onsite role 5 days a week. We will consider entry-level. !! Must be a US Citizen or Greencard Holder - there is no sponsorship available !! We are looking specifically someone who is motivated to do lab work that helps support company marketing campaigns and customer demos. Someone who can be a core part of their marketing and customer teams, helping them do the lab work to make good content. This person will also support customer activities. It should be a fun role for someone who is creative, but wants to be hands on in the lab. Salary range for Lab Technicians is $59K-$79K depending on experience. Keywords: Chemical Chemist Chemistry Materials Science Polymers Plastics Coatings

Piper Health & Sciences is seeking a full-time iPSC Production Scientist to join a growing organization's Bio/Engineering Production team onsite at their Massachusetts location. The ideal candidate will have a strong biology background and hands-on experience in iPSC stem cell culture, differentiation, and QC within a pharmaceutical or biotech environment. Responsibilities of the iPSC Production Scientist Include: * Full-time onsite schedule: Monday-Friday, 9:00 AM - 5:00 PM * Lead and support iPSC production and related lab activities * Perform hands-on stem cell culture and differentiation * Execute QC-related tasks in accordance with SOPs * Maintain accurate lab documentation and records * Support Bio/Engineering Production workflows * Follow all safety, GMP, and GLP standards Qualifications of the iPSC Production Scientist Include: * Biology degree is strongly preferred (Biomedical Engineering degrees are NOT a fit) * Proven hands-on experience with: * iPSC cell culture * Stem cell differentiation * Quality Control (QC) processes * Pharmaceutical or biotech industry experience preferred Compensation of the iPSC Production Scientist Includes: * Salary Range: $83,200.00 - $114,000.00 per year (equivalent to $40.00 - $55.00 per hour), based on experience and certifications. * Comprehensive Benefits: CIGNA Medical, Dental, Vision; 401k through ADP and sick leave as required by law. * Ability to work with a well renowned and growing organization that has a robust pipeline and quality culture. This job opens for applications on 1/12/2026. Applications for this job will be accepted for at least 30 days from the posting date. #LI-AW1 #LI-ONSITE keywords: Scientist, iPSC Production, stem cell culture, induced pluripotent stem cells, cell differentiation, quality control, QC, laboratory scientist, cell biology, biotechnology, pharmaceutical production, bioengineering, GMP, GLP, SOP compliance, tissue engineering, regenerative medicine, bioprocessing, cell therapy, stem cell research, lab operations, onsite scientist, Medford MA jobs, contract scientist, PhD biology, master's biology, postdoctoral research, biotech scientist, pharma scientist, cell culture specialist, stem cell specialist, iPSC scientist, QC scientist, bio production scientist, laboratory techniques, cell-based assays, biotech careers, pharma careers, stem cell manufacturing, cell culture workflows, life sciences jobs, biopharma jobs, laboratory compliance, scientific documentation, biotech industry experience, pharmaceutical industry experience, cell line development, research scientist, production scientist, laboratory QC, stem cell differentiation protocols, cell culture maintenance, full-time onsite scientist, bioengineering production team, regenerative biology, tissue culture, cell therapy manufacturing, biotechnology research, pharmaceutical QC, biomanufacturing, cell biology techniques, stem cell QC testing, scientific method, laboratory safety standards, GMP compliance, GLP compliance, biotech contract role, scientist contract position, iPSC culturing, stem cell production, biotech Medford MA, pharma Medford MA, scientific careers, laboratory scientist jobs, cell therapy scientist, bioprocess scientist, QC laboratory scientist, stem cell lab work, biotech production workflows, pharmaceutical production workflows, life sciences contract jobs, biotech contract scientist, pharma contract scientist.

Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients. We are PCI. Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI. This position will have the primary responsibility for daily formulation activities to ensure schedule activities are completed, formulation materials and equipment are maintained, as well as the responsibility for performing corrective and preventative actions. As a secondary function, provide troubleshooting expertise for manufacturing of products both internally and externally of the company. Schedule: Sunday - Wednesday 6:00AM - 4:30PM Essential Duties and Responsibilities: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The basic duties and responsibilities include the following, but other duties may be assigned. Has ownership for the daily formulation activities to ensure scheduled all scheduled tasks/events are completed Is responsible for critical steps in the formulation process including but not limited to, lab setup and process flows, in-process testing, API dissolution and final QS while ensuring safety, batch integrity and prevention or errors that could lead to product and or finical loss Initiate the production of batch documentation used for engineering and cGMP production. Prepare and update Master Production Batch records and SOPs accurately for communicating and initiate the documentation change process for needed documentation changes Complete executed Batch Records accurately and completely prior to submission to supervision for review Comply with all area SOPs and ensure logbooks are completed, and adhere to cGMP requirements Author process deviations when these occur within the department, participate in investigations, and contribute to identifying corrective and preventative actions Cross train to increase technical skills across the department Accountable for timely communication to management and clients of issues, challenges as well as opportunities for process improvements. As a member of the manufacturing team, you will perform other manufacturing tasks for example filling, capping etc., as needed. Work with enabling groups to improve/implement processes. Other duties as assigned. Strong interpersonal skills Strong working knowledge of MS Office suite is preferable Attention to detail and positive attitude are key attributes Able to follow rules and regulations perfectly Works directly with aseptic and non-aseptic personnel. Works closely with Quality Assurance, MTS, Validation etc. Qualifications: The requirements listed below are representative of the knowledge, skill, and/or ability required for the stated position. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Required: High School education or AS degree or BS degree in Chemical Engineering/ Bio Chemistry or other industry related discipline is preferred Experience and knowledge of formulation/compounding tools and equipment Minimum 1-2 year's work experience in a GMP environment preferably in fill finish pharmaceutical operations Demonstrated ability to prioritize multiple projects and activities Full Professional Proficiency: Ability to speak, read, and write fluently and accurately on all levels pertinent to professional needs. #LI-KC1 Join us and be part of building the bridge between life changing therapies and patients. Let's talk future Equal Employment Opportunity (EEO) Statement: PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status. At PCI, Equity and Inclusion are at the core of our company's purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity - at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture.

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description JobDescription: Skills: Must be detail-orientedand able to work with a high volume of documents in a fast-paced environment.Be highly organized and process-oriented. PreferredQualifications: Additional Information Best Regards, Sneha Shrivastava ***********

Nova Biomedical: One Global Brand. One Vision. Together under one name. Advanced Instruments and Nova Biomedical are now united under one brand, Nova Biomedical, marking a major milestone in our journey to deliver greater value to our customers. By combining our strengths, we're accelerating innovation, supporting critical workflows, and delivering world-class service across the biopharmaceutical and clinical markets. About the company At Nova Biomedical, we re not just building instruments, we re powering breakthroughs that improve lives. Our smart, science-driven solutions are trusted in over 100 countries to speed drug development and enhance patient care. Our integration brings together more than 70 years of scientific excellence with Nova s cutting-edge innovation, forming a powerhouse of precision, purpose, and possibility. With FDA-registered, ISO-certified manufacturing, more than 125 FDA approvals, and industry-trusted diagnostics, we re setting new standards in quality and reliability. Nova Biomedical is proud to be a global leader in osmolality testing and biotechnology and in vitro diagnostic (IVD) instrumentation, dedicated to advancing patient care and scientific discovery with a legacy that continues to shape the future of life sciences. With headquarters in Norwood and Waltham, Massachusetts, and a global team of nearly 2,000 employees, we re building a collaborative, empowered culture grounded in shared values: Customer Centricity, Ingenuity, Ownership & Accountability, Collaboration, and Integrity. Working at Nova Biomedical means joining a mission-driven organization where your contributions matter. Whether you're in engineering, science, manufacturing, or support, you ll be part of a team that values innovation, invests in your growth, and is committed to making a real-world impact on global health. Explore what s next with us at novabiomedical.com or aicompanies.com About the role Responsible for hands on laboratory testing and analysis of test samples and ensuring the overall quality of processes, raw materials, and finished products. If you re passionate about quality control chemistry and want to be part of a team that is shaping the future of life sciences, we d love to hear from you, apply today! What you ll do Works closely with others in a team environment within the Quality Control laboratory and acts as an integral team member on multidisciplinary teams that provide support for Manufacturing and Product Development activities. Completes activities in compliance to applicable SOPs, specifications, and compendia requirements in an efficient and high-quality manner. Performs testing, analysis, and data reporting for test samples. Executes analytical methods for testing on a variety of test samples including raw materials, in-process/finished product, stability, validation, and R&D test samples. Prepares and standardizes laboratory reagents and test solutions. Documents all work in compliance with Good Documentation Procedures. Generates data reports and forms. Operates, calibrates, keeps track of preventative maintenance schedule for all laboratory equipment. Supports and executes activities for test method validation and transfer. Authors, edits, and reviews technical reports, protocols, specifications, and SOPs. Continually reviews programs and systems to develop and drive improvements in efficiency, effectiveness, and quality. Participates in and/or leads independent and team-based investigations. Determines root causes for out of specification and atypical results. Develops, proposes, and monitors corrective actions. Supports customer complaint investigations as required. Performs all work according to applicable safety procedures using good laboratory techniques and using safe operation of laboratory equipment. Performs departmental tasks assigned, chemical inventory, ordering of consumables and lab supplies, disposal of waste, dishwashing, general lab organization and cleaning. Leads hands on training of analytical techniques. Acts as peer technical and quality assurance review for laboratory work performed. Collates, analyzes, and summarizes data. When required, interacts with internal and external auditors. What we are looking for in you 2+ years related experience and/or training; or equivalent combination of education and experience. Must be able to use Microsoft Excel, Word, and Access, as well as Company Software. Associate degree (A.A.) or equivalent for a two-year college or technical school. Physical Requirements for this role include: Typical of office environment. Must be able to use basic office equipment: Computer, printer/copier, telephone, etc. Must be able to remain stationary for long periods of time. Must be able to communicate with stakeholders through various means. The full list of physical requirements for this role is available upon request. Why work for Nova Biomedical Flexible Medical, Dental, & Vision Coverage Competitive 401k company match Bonus Program, Generous PTO and paid holidays Generous Tuition reimbursement Hybrid and flexible work arrangements (job specific) Professional development, engagement and events Company marketplace for lunch and snacks! (location specific) Company subsidized cafeteria (Waltham) Work Location: On-site in Norwood Schedule/Hours: Monday to Friday, 7:30am - 4:00pm Targeted Salary Range: $75k - $80k Nova Biomedical believes in transparency and integrity throughout all we do, including compensation. The provided salary range for this role represents the expected base salary or hourly rate for this opening. Actual compensation will be commensurate with the candidate s experience and may vary based on individual factors such as location, skills, and education. EEO Statement: Nova Biomedical takes pride in being an equal opportunity employer committed to hiring a diverse and inclusive workforce. As a part of our commitment to a diverse and inclusive workforce, Nova Biomedical will continue to take steps to assure that recruitment, hiring, assignment, promotion, compensation, and all other personnel decisions are made and administered without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, gender expression, veteran status, age, mental or physical disability, genetic information or any other protected class. *******************************************************************

Global Channel Management is a technology company that specializes in various types of recruiting and staff augmentation. Our account managers and recruiters have over a decade of experience in various verticals. GCM understands the challenges companies face when it comes to the skills and experience needed to fill the void of the day to day function. Organizations need to reduce training and labor costs but at same requiring the best "talent " for the job. Job Description Perform a variety of analytical laboratory testing of raw materials and assure compliance with applicable laws, rules and regulations. Major Job Duties: Operate a variety of treatment test equipment, such as HPLC, spectrophotometer, pH meter, filtration devices, hot plates, TDS, Moisture Apparatus, Melting Point, balances, etc. Conduct a variety of analytical lab tests in compliance with standard testing methods, procedures and regulations; implement quality control specifications. Set up instruments and conduct sample tests; utilize a variety of methods to assure compliance to established standards and testing controls; interpret test results and prepare and submit reports related to test results. Perform, interpret, evaluate and record standard process control laboratory tests on ; perform calculations as needed and record results; notify appropriate personnel of abnormal or critical results and significant changes in lab results. Troubleshoot, clean and maintain instruments, glassware and equipment; conduct preliminary diagnostic test on equipment; assure materials meet standards of cleanliness to assure accurate test results; assure an adequate supply of test materials to perform daily testing; perform preventive maintenance on equipment. Qualifications WET CHEMISTRY GMP COMPENDIAL TESTING BS IN SCIENCES Additional Information $32/hr 9 MONTHS

HiFyve is hiring a Wet Chemistry Lab Technician for a Manufacturing company in Andover, MA!! Pay Rate- $22-$25/hr. Shift: Sun - Thur 12 am to 8 am Job Summary: This individual will work in the wet chemistry process lab to support all plating fabrication operations. The candidate will work with the wet chemistry lab team for day to day production analysis as well as special projects. Job Description Perform basic chemical analysis techniques. Utilize chemical analysis equipment to include Auto-Titration, CVS, ICP, and UV-VIS. Ability to input analysis results into TrueChem. Maintain lab safety policies and procedures. Education / Qualifications 1+ years of prior laboratory experience required. Experience with Titration analysis, ICP or AA, UV-VIS. Knowledge of operation and maintenance of lab equipment highly desired. Knowledge of Microsoft Word, Excel, and PowerPoint required. Must pay high attention to detail, possess self-motivating skills, and have the ability to self-inspect for quality and accuracy. Please apply or email your resume to: *********************

We are seeking a passionate PhD-level synthetic chemist to drive the discovery of small molecules for next-generation 3D printing resins. This position involves rapid exploration of chemical space through organic synthesis to develop photochemical and photophysical structure-property relationships. This role will be particularly appealing to chemists with a passion for both synthetic and physical organic chemistry. Our process uses a small amount of each lead candidate, so synthetic creativity is not limited by the scalability concerns that usually narrow the available chemical space in materials applications. Responsibilities Design, execute, and troubleshoot small molecule synthetic routes, with a focus on divergent or modular approaches to rapidly generate lead candidates. Characterize lead candidates via UPLC, NMR, UV/Vis and IR spectroscopy, and mass spectrometry. Contribute to the development of high-throughput analytical capabilities, small molecule databases, and virtual libraries. Work with cross-functional teammates to explore photochemical and photophysical structure-property relationships that drive 3D printing performance. Mentor junior scientists. Maintain excellent electronic lab notebook documentation. Minimum Qualifications PhD in Organic Chemistry or BS in Chemistry and 5+ years of experience in a small molecule discovery role. Strong expertise in both synthetic and physical organic chemistry, demonstrated through publications and other activities. Significant experience designing and executing multi-step synthetic routes. Extensive experience with modern computing and data analysis tools relevant to synthetic chemistry. Excellent communication, organizational, and time management skills. Demonstrated ability to independently drive an idea from conception to project completion. Evidence of strong collaboration and teamwork talents/skills. Strong publication record, both as lead author and as contributor to other projects. Preferred Qualifications Expertise in photochemistry and/or radical chemistry. Significant experience with synthesis of heterocyclic and/or extended aromatic systems, especially those relevant to organic (opto)electronics. Experience with cheminformatics and/or computational chemistry tools (e.g. DFT) relevant to the production of structure-property relationships. Benefits We offer competitive compensation packages in our VC-backed startup. Benefits include a full suite of offerings covering medical, dental, vision and 401k plan. Beautiful setting looking out over a river and seaport; outdoor seating and picnic areas. Highly collaborative work environment. Additional Information Travel: Occasional travel may be required from time to time Location: Boston, Massachusetts We value diversity in our company and are an Equal Opportunity Employer.

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! Job Description We are seeking a candidate that will support a client team that is responsible for developing robust and efficient purification processes of recombinant proteins and other biological therapeutics from early to late stage of development. We are seeking an analytical scientist who will work in a collaborative environment to be engaged in the analysis, monitoring and characterization of in-process samples to support the client in improving process performance by optimizing product recovery and impurity removal. This role will provide routine analytical testing. Knowledge and expertise in analytical biochemical techniques including HPLC (HI-C, RP, SEC, etc.), and Octet are a must. The successful candidate must be self-motivated and able to work independently, be accountable for own results and prioritize own workflow, and seek opportunities to take on new projects. Job Responsibilities and Requirements: Experience with protein chemistry, protein analytics, and bioprocess technology is required Expertise in analytical chemistry using a broad range of separation, chromatographic, spectroscopic and other detection techniques to characterize and monitor protein purification process Hands on experience and working knowledge on techniques including but not limited to liquid chromatography like UPLC/HPLC (size-exclusion, hydrophobic, ion-exchange, affinity), and Octet Hands on experience with SDS-PAGE, ELISA, and experience with protein purification/chromatography at the lab scale is a plus A working knowledge on Empower and/or ChemStation control and data analysis software is strongly preferred Work closely with colleagues by providing quality data to support product development through early clinical phases in a timely manner; uses understanding of analytical tools to assess and interpret experimental data Maintains written records (electronic lab notebooks and databases) of all experimental work in accordance with Good Laboratory Practices Leads in the routine calibration, maintenance, troubleshooting and repair of laboratory instruments, systems or apparatus and may interact with internal site or external vendors in the maintenance and continuous improvement of safe and effective working practices Qualifications Bachelors or Masters Degree in Biotechnology, Biochemical Engineering, Analytical Chemistry, Chemical Engineering or other related discipline BS 2-4 years or MS +0-2 years of relevant experience Experience with HPLC (SEC, HIC, and RP), protein purification methods, and octet Excellent attention to detail and ability to follow procedures to generate reproducible data in a controlled laboratory environment Excellent skills in Microsoft Office, data analysis software, and other related applications Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies Ability to think critically and demonstrate troubleshooting/problem solving skills Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude Authorization to work in the United States indefinitely without restriction or sponsorship Additional Information The position is full-time, on-site, Monday through Friday, 8:00 AM-5:00 PM. Pay range: $27.00 - $31.00 based on degree level and years of relevant experience Excellent full-time benefits including: Comprehensive medical coverage, dental, and vision options Life and disability insurance 401(k) with company match Paid vacation and holidays Ready to take the next step in your career? Apply today and join a team that's making a difference in science every day. Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.