Tech Ops and Quality - Quality Control Analyst II TalentBurst, Inc.Tech Ops and Quality - Quality Control Analyst IINorton, MA$42.58 / hourBy ensuring these critical activities are executed within project milestones and timelines, the Analyst II contributes to manufacturing operations by ensuring timely and accurate testing of incoming raw materials, maintaining documentation, and contributing to continuous improvement initiatives within the laboratory. Maintain up-to-date training records, adhere to the inspection schedule, and ensure the timely completion of all assignments to support the seamless operation of QC activities and uphold the department's commitment to meeting project timelines and quality metrics.
Quality Assurance (QA) Document Control Specialist II Collins Consulting, IncQuality Assurance (QA) Document Control Specialist IIWorcester, MassachusettsFull timeUnder direct supervision, perform day-to-day Document Control activities: Process DCR packages and review for correctness and completeness; monitor and update in-process documents; create, assign and archive QA controlled lab notebooks and logbooks; assist in managing the electronic document management system; assist in managing access to Master Documents in the Document Control Vault; and create reports. Performs duties in support of established records management procedures, including scanning, filing and managing offsite records storage and retrieval.
Senior Engineer, Central Quality & Quality Control | Titleist Acushnet CompanySenior Engineer, Central Quality & Quality Control | TitleistNew Bedford, MassachusettsPartnering cross-functionally with Manufacturing, R&D, Supply Chain, and external suppliers, the Senior Engineer provides technical expertise in root cause analysis, corrective and preventive actions, and new product introductions. The Senior Engineer, Central Quality & Quality Control plays a critical role in driving excellence across manufacturing operations and supplier networks by ensuring consistent product performance and compliance with Acushnet Company Quality System requirements.
Quality Control Finish Line Staffing ServicesQuality ControlMansfield, MAWe are hiring on behalf of our client for a detail-oriented Quality Control Inspector to support incoming, in-process, and final inspections within a medical device manufacturing environment. Perform incoming, in-process, and final inspections following work instructions and inspection plans.
Tech Ops and Quality - Quality Control Analyst I LanceSoft IncTech Ops and Quality - Quality Control Analyst INorton, MA$30.33 / hourThe Analyst I in Quality Control Operations will play a critical role in executing assays, generating accurate and reliable data, and supporting the general operations of the laboratory to ensure the quality and compliance of our products from development through to commercialization. Maintain up-to-date training records, adhere to the testing schedule, and ensure the timely completion of all assignments to support the seamless operation of QC activities and uphold the department's commitment to meeting project timelines and quality metrics.
Quality Control Supervisor Consolidated Precision ProductsQuality Control SupervisorBraintree, MABuild an atmosphere of competence, cooperation and trust with customer representatives via Source Inspection and Supplier Product, Systems and Qualification Surveys. Take active participation in our Continuous Improvement efforts, promote quality excellence and encourage teamwork among ourselves and our customers.
Quality Control Supervisor (Braintree, MA) Consolidated Precision ProductsQuality Control Supervisor (Braintree, MA)Braintree, MABuild an atmosphere of competence, cooperation and trust with customer representatives via Source Inspection and Supplier Product, Systems and Qualification Surveys. Take active participation in our Continuous Improvement efforts, promote quality excellence and encourage teamwork among ourselves and our customers.
Manager, Quality Control Consultant The Steely GroupManager, Quality Control ConsultantHybrid, Waltham, MAThe selected candidate will work collaboratively with Analytical Quality Control leaders to assess laboratory conformance with cGMPs, and with CMC Regulatory Affairs and Quality Assurance to ensure the translational accuracy and integrity of data incorporated into Module 3 sections of CTD regulatory submissions and written responses to regulatory authorities. Contribute to regulatory and technical documentation by reviewing QC data for accuracy, completeness, and traceability; verifying data transcription and data checks supporting regulatory submissions; and ensuring information is ready for inclusion in internal reports, APQRs, Module 3 submission-supporting documents, and responses to regulatory authorities.
Quality Control Technician ManpowerQuality Control TechnicianFranklin, MAp> ManpowerGroup® (NYSE: MAN), the leading global workforce solutions company, helps organizations transform in a fast-changing world of work by sourcing, assessing, developing, and managing the talent that enables them to win. We are recognized consistently for our diversity - as a best place to work for Women, Inclusion, Equality and Disability and in 2023 ManpowerGroup was named one of the World's Most Ethical Companies for the 14th year - all confirming our position as the brand of choice for in-demand talent.
Associate Director, Quality Control Lab Automation ModernaTXAssociate Director, Quality Control Lab AutomationNorwood, MassachusettsWe are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S. If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit modernatx.com/careers to learn more about our current opportunities. The Associate Director, Quality Control Lab Automation Strategy & Digital Integration is responsible for leading the strategy, implementation, and lifecycle management of laboratory automation and digital integration across Moderna’s Quality Control laboratories.
Recording/ Quality Control Specialist The Silk CompaniesRecording/ Quality Control SpecialistWarwick, Rhode IslandThe Recording/ Quality Control Specialist works as part of a team to ensure that all closing conditions, as laid out by the lender or their investor, are met after signing and that all transactions are disbursed timely as scheduled. Silk Title Co. is a privately owned, fast-growing company which handles billions of dollars a year in real estate transactions for some of the nation’s top fin-tech institutions.
Senior Manager/Associate Director, Quality Control Xenon PharmaceuticalsSenior Manager/Associate Director, Quality ControlNeedham, MassachusettsLead the assigned program’s stability activities, including trending, statistical evaluation, and scientific interpretation of stability data to assess product performance throughout its lifecycle, support shelf-life extensions and expiry dating justifications, and proactively identify and evaluate emerging stability risks and trends. Our Total Rewards program includes base salary, target bonus, and stock options, as well as a full range of benefits including medical, dental, vision, short-& long-term disability, accidental death & dismemberment, and life insurance programs, Employee Assistance Program, travel insurance, and retirement savings programs with company matching contributions.
Vice President, Quality Control Candel TherapeuticsVice President, Quality ControlNeedham, MA$290,000–$335,000 / yearPosition SummaryThe Vice President, Quality Control will provide strategic, technical, and operational leadership for all Quality Control functions supporting the development, manufacture, release, and lifecycle management of viral vector and advanced therapy products. This role will work closely with CMC leadership, Analytical Development, Process Development, Manufacturing, Quality Assurance, Regulatory Affairs, Clinical Development, Supply Chain, Program Management, external laboratories (CROs/CDMOs), and executive leadership.
Quality Control (QC) Chemist Inhalation Products (MDI Focus) Aequor Technologies LLCQuality Control (QC) Chemist Inhalation Products (MDI Focus)Fall River, MA$65,000–$105,000 / yearAs a QC Chemist specializing in inhalation products, you’ll play a vital role in ensuring the safety, quality, and performance of metered dose inhalers (MDIs) and related dosage forms that patients rely on every day. This is not your average QC role—here, you’ll work on complex aerosol and particle-based delivery systems, applying advanced analytical techniques to confirm product integrity and regulatory compliance in a highly controlled cGMP environment.
Quality Control (QC) Chemist LifelancerQuality Control (QC) ChemistFall River, Massachusetts$65,000–$105,000 / yearAbout InvaGen Pharmaceuticals, a Cipla subsidiary InvaGen Pharmaceuticals, Inc. is engaged in the development, manufacture, marketing, and distribution of generic prescription medicines with focus on a range of therapeutic areas, including cardiovascular, anti-infective, CNS, anti-inflammatory, anti-diabetic, and anti-depressants. Over the last eight decades, we have strengthened our leadership in India’s pharmaceutical industry and fortified our promise of strengthening our global focus by consolidating and deepening our presence in the key markets of India, South Africa, the U.S., and other economies of the emerging world.
Senior Scientist I, Quality Control Candel TherapeuticsSenior Scientist I, Quality ControlNeedham, MAThis position collaborates with external manufacturing and tech transfer and is focused on Adenovirus and Herpesvirus vectors, associated cell-based potency assays, as well as performing training of new technical staff and troubleshooting and validation of new and established assays. A strong background in one or more analytical techniques such as various HPLC based methods, microplate UV/Vis/Luminescent assays, cell-based assays including virus quantification and potency, qPCR, electrophoresis, sizing techniques such as DLS, etc. .
Vice President, Quality Control Candel Therapeutics Inc.Vice President, Quality ControlNeedham, MA$290,000–$335,000 / yearThe Vice President, Quality Control will provide strategic, technical, and operational leadership for all Quality Control functions supporting the development, manufacture, release, and lifecycle management of viral vector and advanced therapy products. This role will work closely with CMC leadership, Analytical Development, Process Development, Manufacturing, Quality Assurance, Regulatory Affairs, Clinical Development, Supply Chain, Program Management, external laboratories (CROs/CDMOs), and executive leadership.
Quality Control I (2nd Shift) MOOQuality Control I (2nd Shift)East Providence, RIYour value to the business lies in your ability to identify, contain, and solve quality problems before they impact our customers, directly contributing to MOO's reputation for high-quality, delightful products and supporting our continuous improvement goals. Those customers are typically small and medium-sized businesses based in North America, the UK, and Europe – businesses that, like us, value design and see the brand-building power of putting something real in people’s hands.
Quality Control Technical Services Analyst IV RD PartnersQuality Control Technical Services Analyst IVNorton, Massachusetts$114,227–$142,827S. in chemistry, biology, or biochemistry, or related scientific field; advanced degrees considered; Pharmaceutical/Biotech industry experience with 8-12 years in a GMP Quality Control function or equivalent, relevant industry experience. Support and sometimes lead investigations into analytical and product-related quality deviations, employing root cause analysis and implementing corrective and preventive actions (CAPAs) to mitigate risks and enhance quality.
Quality Control Admin Finish Line Staffing ServicesQuality Control AdminMansfield, MAThis position is ideal for someone who enjoys reviewing documentation, ensuring accuracy, and supporting quality processes that help deliver compliant, high-quality products. In this role, you will review manufacturing documentation, inspect product labeling, verify test data, and ensure all records meet ISO 13485 and FDA regulatory requirements.