Principal Associate I, Plant Quality Assurance - 2ND SHIFT ReplimunePrincipal Associate I, Plant Quality Assurance - 2ND SHIFTFramingham, MassachusettsThe Principal Associate I/II, Plant Quality Assurance (PQA) reports to the Associate Director, Quality Assurance and is responsible for on-going Quality oversight to ensure real time quality oversight for Drug Substance, Drug Product, and all other production and QC testing activities according to current good manufacturing practices (cGMP), good documentation practices (GDP) and other applicable regulations. The RPx platform is designed to have a unique dual local and systemic activity consisting of direct selective virus-mediated killing of the tumor resulting in the release of tumor derived antigens and altering of the tumor microenvironment to ignite a strong and durable systemic response.
Product Quality Engineer VulcanForms IncProduct Quality EngineerMA$75,000–$94,000 / yearFounded in 2015 to develop the world's first industrially scalable laser metal additive manufacturing solution, VulcanForms is reshaping how the world manufactures critical products. We foster an inclusive culture where people take ownership, solve meaningful problems, and continuously learn, because we believe diverse perspectives lead to better outcomes.
Quality Engineer MACOM Technology Solutions Holdings IncQuality EngineerLowell, MAThey will also provide operations support for Asia in terms of SAP inventory control, running metrics report for the team, release of shipping holds in SAP and providing general guidance and training to the team in Quality inventory control. Specific responsibilities: Be first line of contact for Passive product customer quality issues including monitoring of New Product Development quality evaluations.
Senior QA Specialist Editas Medicine, Inc.Senior QA SpecialistCambridge, MA$110,000–$120,000 / yearDecoding The Role: The primary focus of this role in the next 12 months is to advance our lead in vivo development candidate, EDIT-401, into the clinic to establish human proof of concept by ensuring compliance with FDA, cGMP, and international regulatory requirements across manufacturing, testing, product disposition, and quality event management. Author, review, and approve GMP documentation (SOPs, batch records, protocols, technical reports, test methods, specifications, and summary reports) supporting GMP manufacturing.
Regional Quality Manager, Southwest (Remote - Travel Required) SOLV Energy LLCRegional Quality Manager, Southwest (Remote - Travel Required)MARemote$116,812–$146,016 / yearIn addition, candidate introductions or resumes can only be submitted to our internal talent acquisition recruiting team if a signed vendor agreement is already on file and the third-party recruiter or agency has received formal instructions from our internal talent acquisition team to submit candidates for a particular job posting. Train and support: Provide direct training and guidance to project teams on quality assurance and control practices, SOLV Energy's Quality SOP's, SWI's, MOP's and reference guides, ensuring that all team members understand and follow established procedures.
Quality Engineering Manager Honeywell International IncQuality Engineering ManagerWoonsocket, RIAs a trusted partner, we provide actionable solutions and innovation through our Aerospace Technologies, Building Automation, Energy and Sustainability Solutions, and Industrial Automation business segments - powered by our Honeywell Forge software - that help make the world smarter, safer and more sustainable. Honeywell's Industrial Automation business unit provides advanced automation control, sensing, and software solutions that improve operational efficiency, safety, and reliability for customers in manufacturing, energy, and process industries worldwide.
Manager, Regulatory/Quality Systems BlockHiresManager, Regulatory/Quality SystemsNashua, New HampshireLead the development of SOPs and work instructions and associated quality tools to improve product quality and to increase work efficiency Identifying opportunities for improvement and developing processes to ensure regulatory compliance and process robustness. 8+ years quality and regulatory experience; 3+ years in a leadership role in a multiple or large site (600+ employees and associated revenue/customer base).
Director, Quality Electric Hydrogen CoDirector, QualityMA$192,270–$226,200 / yearOperationalize and continuously improve core quality processes, including Non-Conformance Reporting (NCR), Incoming Quality Control (IQC), Material Review Board (MRB), and Corrective and Preventive Actions (CAPA). Professional certifications such as ASQ CQE, CQA, CMQ/OE, Lean Six Sigma Black Belt, ISO Lead Auditor, or equivalent quality certifications strongly preferred.
Quality Assurance Specialist Nova Biomedical CorpQuality Assurance SpecialistBillerica, MA$77,000–$86,000 / yearThis role works cross-functionally to maintain an inspection-ready QMS, ensure compliance with regulatory and quality requirements, support implementation of external requirements, and drive continuous improvement initiatives that enhance overall quality system performance and operational effectiveness. With headquarters in Norwood and Waltham, Massachusetts, and a global team of nearly 2,000 employees, were building a collaborative, empowered culture grounded in shared values: Customer Centricity, Ingenuity, Ownership & Accountability, Collaboration, and Integrity.
Quality Assurance Specialist Dana-Farber Cancer Institute IncQuality Assurance SpecialistBOSTON, MA$98,500–$109,100 / yearAble to work independently on off-shifts, capable of handling stress of producing accurate results under time constraints; willing to accommodate schedule adjustments, as well as off-shift and weekend assignments as workload dictates. We strive to create an inclusive, diverse, and equitable environment where we provide compassionate and comprehensive care to patients of all backgrounds, and design programs to promote public health particularly among high-risk and underserved populations.
Quality Technician Bio-Techne CorpQuality TechnicianMA$23.20–$31.90 / hourIn addition to universal responsibilities, Quality Technician will have Devens site specific responsibilities including but not limited to: Performs facility monitoring tasks including: o Daily monitoring of temperature-controlled areas using calibrated devices. Why Join Bio-Techne: We offer competitive insurance benefits starting on day one: medical, dental, vision, life, short-term disability, long-term disability, pet, and legal and ID shield.
Clinical Laboratory Quality Coordinator - Onsite LabCorpClinical Laboratory Quality Coordinator - OnsiteWestborough, MA$26–$30 / hourAs we shape the future of healthcare, we are leveraging advanced technologies, intelligent digital solutions and data-driven innovation across our operations to enhance how work gets done and deliver greater value to customers and patients. Labcorp is a global leader in laboratory services, providing the insights and answers that help healthcare providers, patients, researchers, pharmaceutical companies and health systems make confident decisions and improve outcomes.
Senior Product Quality Engineer, Consumer Technology VulcanFormsSenior Product Quality Engineer, Consumer TechnologyDevensThe Senior Product Quality Engineer, Consumer Technology manages quality systems, implements robust process controls, and drives continuous improvement across advanced manufacturing programs within our consumer technology business unit. Root Cause & CAPA: Independently investigate complex product non-conformances (NCRs), lead material review boards (MRBs), and drive the execution of Corrective and Preventive Actions (CAPAs) to eliminate systemic failure modes.
Operational Area Senior Quality Specialist (Contract)502 Vertex PharmaceuticalsOperational Area Senior Quality Specialist (Contract)502Boston, Massachusetts$55–$65 / hourFull timeAgreeing to the Atrium Terms and Conditions, includes permission to use the email address and mobile phone number you provide during the application process or throughout the duration of your prospective or actual employment to notify you of job openings, profiles, articles, news, and other employment-related information, as well as to notify you of special promotions or additional products and services offered by us or our affiliates and partners. Job Description: The Operational Area Senior Quality Specialist will provide QA support of manufacturing operations, analytical laboratory operations and materials management for the external manufacturing programs at VCGT.
Product Quality Engineer VulcanFormsProduct Quality EngineerDevensPreferred: Experience with ISO 13485, ISO 9001, or AS9100; experience in additive manufacturing or regulated industries (Medical Device/Consumer Electronics). The Product Quality Engineer plays a hands-on role in supporting product quality and regulatory compliance for advanced metal additive manufacturing.
Senior Associate, Quality Assurance Ocular Therapeutix IncSenior Associate, Quality AssuranceBedford, MA$109,000–$121,000 / yearPosition Summary: The Senior Associate, QA will work in collaboration with all departments within Ocular, to provide the necessary Quality Assurance (QA) oversight for the production of Drug Products including support of end-to-end operations from technology transfer and clinical production all the way through commercialization. Ocular Therapeutix, Inc. (NASDAQ:OCUL) is a biopharmaceutical company focused on the formulation, development, and commercialization of innovative therapies for diseases and conditions of the eye using its proprietary bioresorbable hydrogel-based formulation technology, ELUTYX.
NewQuality Specialist Micro Tech Staffing GroupQuality SpecialistWeymouth, MAContinuous improvement practices throughout manufacturing process and assisting departments with quality inspections or oversight as needed. We are looking for an eager and motivated individual for a great opportunity to learn and grow long term!
NewQA Inspector Micro Tech Staffing GroupQA InspectorNorth Andover, MAUses precision measuring tools, reads engineering drawings, documents inspection results, identifies nonconforming materials, supports ISO 9001 quality processes, performs internal quality audits, and maintains accurate quality records to ensure compliance and continuous improvement.
Quality Assurance Technician Actalent IncQuality Assurance TechnicianBurlington, MA$30–$40 / hourWe are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing winner for both client and talent service. In this role, you will be responsible for reviewing and verifying Quality Control (QC) data, ensuring documentation accuracy, and supporting batch record and patient record review activities.
Senior Quality Scientist I AddgeneSenior Quality Scientist IWatertown, MAFull timeAs an “Addgenie”, you will work collaboratively with internal teams to help fulfill this mission, including scientists, software engineers and product developers, renowned customer support teams, scientific content creators, and business development professionals. Since its founding in 2004, Addgene has grown and innovated in order to assist the research community by archiving and sharing useful DNA-based research materials and resources (such as plasmids, viral vectors, and recombinant antibodies) with scientists worldwide.