Site Quality Manager, Consumer Technology VulcanForms IncSite Quality Manager, Consumer TechnologyMA$122,400–$168,300 / 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. Act as the primary technical advisor for the lab, resolving difficult to moderately complex problems regarding measurement strategy, equipment downtime, or inspection/test bottlenecks.
System Analyst & Validation Engineer Siemens HealthineersSystem Analyst & Validation EngineerWalpole, MAFull timeAs a key contributor in a dynamic manufacturing and software development landscape, you will: Serve as the subject matter expert for a multi-site Test Data Management System (TDMS) (Specialized in house application) that serves as Lab Information Management Systems (LIMS) and Labeling Systems (Product Labels and Inserts supplied by the Manufacturer) that generates digital and paper-based materials. "It is Siemens Healthineers' policy to comply fully and completely with all United States export control laws and regulations, including those implemented by the Department of Commerce through the Export Administration Regulations (EAR), by the Department of State through the International Traffic in Arms Regulations (ITAR), and by the Treasury Department through the Office of Foreign Assets Control (OFAC) sanctions regulations.".
Scientist, Analytical Sciences and Technology Moderna IncScientist, Analytical Sciences and TechnologyNorwood, MA$109,200–$174,600 / yearWe 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 Candidate will serve as a key technical resource across the analytical network, collaborating with Quality Control, Quality Assurance, Regulatory Affairs, Manufacturing Sciences, and Contract Manufacturing Organizations (CMOs) to ensure robust analytical performance, compliance, and inspection readiness.
Sr. Quality Specialist, GxP Document Control Bicara TherapeuticsSr. Quality Specialist, GxP Document ControlBoston, MassachusettsFICERA specifically addresses a key challenge in solid tumor treatment by enabling immune cell penetration into tumors, reducing fibrosis and immunosuppression while reversing TGF--driven resistance mechanisms - ultimately designed to drive the deep, durable responses that may translate into better outcomes and survival for patients. Founded in 2020, we've built a global team of over 100 employees headquartered in Boston, with a clear focus on advancing our lead asset, ficerafusp alfa, or FICERA - a potentially first-in-class bifunctional EGFR-directed antibody combined with a TGF- ligand trap.
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.
NewSenior Medical Laboratory Scientist, Blood Bank - Evening Shift Mass General BrighamSenior Medical Laboratory Scientist, Blood Bank - Evening ShiftBoston, MassachusettsNo Licenses and Credentials Medical Technologist (ASCP) [MLT, MT, MLA, Histologists] - American Society for Clinical Pathology Board of Certification (ASCP-BOC) required Experience lab experience 3-5 years required Knowledge, Skills and Abilities - The knowledge, both practical and theoretical, of tests and procedures necessary to review findings and advise and direct subordinates in action. The Medical Laboratory Scientist, Senior I, in their role as Technical Supervisor, Technical Consultant, or General Supervisor as defined by CLIA, may be delegated responsibility for the technical oversight of the laboratory, including day-to-day supervision of operations and personnel performing testing and reporting results.
Senior Medical Laboratory Scientist, Blood Bank - Day Shift Mass General BrighamSenior Medical Laboratory Scientist, Blood Bank - Day ShiftJamaica Plain, MassachusettsThe Medical Laboratory Scientist, Senior I, in their role as Technical Supervisor, Technical Consultant, or General Supervisor as defined by CLIA, may be delegated responsibility for the technical oversight of the laboratory, including day-to-day supervision of operations and personnel performing testing and reporting results. Under the general supervision of the Technical Director and Clinical Supervisors, the Senior Technologist I oversees assigned workstations, including Quality Control (QC) review, training, competency assessment of staff, and inventory management.
Nuclear Pharmacist Mass General BrighamNuclear PharmacistBoston, MassachusettsPerforms complex analytical testing on manufactured and/or compounded radiopharmaceutical including, thin layer chromatography (TLC), high performance liquid chromatography (HPLC), gas chromatography (GC), radionuclide identity and purity testing with high purity germanium solid state detectors, sterility and pyrogen testing. Under direction of the Senior Operations Manager, PET Production and Cyclotron, the nuclear pharmacist provides a variety of services, ensuring compliance in the procurement, preparation, compounding, manufacturing, quality control testing, dispensing, distribution, and monitoring of radiopharmaceuticals.
Quality Assurance Integrated Resources, IncQuality AssuranceAndover, MassachusettsContractorQualificationsMinimum BS in biology, engineering or related sciences with at least 3 years of pharma/biopharma experience in a QA or validation roleStrong working knowledge of global GMPs with emphasis on validation, including computer validationStrong interpersonal, oral and written skillsAdditional InformationWe do have referral bonus of $500 per candidate, if you refer any of your friends or colleague who are looking out for the same job. Successful candidate requires a strong working knowledge of global GMPs with an emphasis on validation lifecycle including computer system validation, 21 CFR Parts 210 and 211, and Part 11, Electronic Records and Electronic Signatures.
NewDirector/Associate Director, Quality Management Systems Corbus Pharmaceuticals Holdings IncDirector/Associate Director, Quality Management SystemsNorwood, MAAbout Corbus: Corbus Pharmaceuticals Holdings, Inc. is a clinical-stage company focused on oncology and obesity and is committed to helping people defeat serious illness by bringing innovative scientific approaches to well-understood biological pathways. Oversee the end-to-end lifecycle management of quality documents, including policies, SOPs, and related controlled records, ensuring consistency, accuracy, and compliance with applicable regulations that achieves inspection readiness.
MRI Technologist, QA Specialist Brigham and Women's HospitalMRI Technologist, QA SpecialistBoston, MA$52–$56.59 / hourReporting to the MRI Quality Assurance Manager, the MRI Quality Assurance specialist will assist with the MRI Quality Assurance program by collecting data, implementing new protocols and provide appropriate education to the staff. The framework is comprised of ten competencies (half People-Focused, half Performance-Focused) and are defined by observable and measurable skills and behaviors that contribute to workplace effectiveness and career success.
Associate Iii, Quality Technical Product Complaints Biogen IdecAssociate Iii, Quality Technical Product ComplaintsCambridge, MA$73,000–$95,000 / yearRegular employees are eligible to receive both short term and long-term incentives, including cash bonus and equity incentive opportunities, designed to reward recent achievements and recognize your future potential based on individual, business unit and company performance. Knowledge of Product Complaint systems/operations and cGMP requirements for biologics, oral-dose products, medical devices, drug delivery devices, and combination products.
Associate III, Quality Technical Product Complaints BiogenAssociate III, Quality Technical Product ComplaintsCambridge, Massachusetts$73,000–$95,000 / yearRegular employees are eligible to receive both short term and long-term incentives, including cash bonus and equity incentive opportunities, designed to reward recent achievements and recognize your future potential based on individual, business unit and company performance. The base compensation range for this role is: $73,000.00-$95,000.00 Base salary offered is determined through an analytical approach utilizing a combination of factors including, but not limited to, relevant skills & experience, job location, and internal equity.
Quality Assurance Specialist Emerson Electric CoQuality Assurance SpecialistMansfield, MA$60,000–$68,000 / yearWe have built an engaged community of inquisitive, dedicated people who thrive knowing they are welcomed, trusted, celebrated, and empowered to solve the world's most complex problems - for our customers, our communities, and the planet. Through our deep domain expertise and legacy of flawless execution, Emerson helps customers in critical industries like life sciences, energy, power and renewables, chemical and advanced factory automation operate more sustainably while improving productivity, energy security and reliability.
Quality Engineer I Freudenberg GroupQuality Engineer IBeverly, MASupports plant activities in process validation, process capability issues and customer issues, initiates corrective and preventive action, with an eye to increased capability, reduced inspection time/effort, customer satisfaction and supports Quality System implementation. Performs/leads with the investigation of root cause and determination of corrective and preventive actions relating to NCMRs and CAPAs Interfaces with manufacturing and engineering to resolve quality issues for new and existing product lines.
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.
Quality Assurance Specialist - Supplier Quality Actalent IncQuality Assurance Specialist - Supplier QualityHopkinton, MA$38–$40 / hourExperience supporting supplier quality activities, including supplier qualification and assessments, performance monitoring, corrective and preventive action (CAPA) management, and change control processes. We 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.
Laboratory Production Technician Siemens HealthineersLaboratory Production TechnicianWoburn, MAFull timeIt is Siemens Healthineers' policy to comply fully and completely with all United States export control laws and regulations, including those implemented by the Department of Commerce through the Export Administration Regulations (EAR), by the Department of State through the International Traffic in Arms Regulations (ITAR), and by the Treasury Department through the Office of Foreign Assets Control (OFAC) sanctions regulations.". At Siemens Healthineers , we operate the world's largest PET radiopharmaceutical network - delivering over 1 million doses annually with a >99% fulfillment rate and supporting more than 2,800 imaging centers worldwide.
Pharmaceutical Laboratory Technician Siemens HealthineersPharmaceutical Laboratory TechnicianWoburn, MAFull timeIt is Siemens Healthineers' policy to comply fully and completely with all United States export control laws and regulations, including those implemented by the Department of Commerce through the Export Administration Regulations (EAR), by the Department of State through the International Traffic in Arms Regulations (ITAR), and by the Treasury Department through the Office of Foreign Assets Control (OFAC) sanctions regulations.". At Siemens Healthineers , we operate the world's largest PET radiopharmaceutical network - delivering over 1 million doses annually with a >99% fulfillment rate and supporting more than 2,800 imaging centers worldwide.
Manager, Quality Operations Viridian Therapeutics IncManager, Quality OperationsWaltham, MAIn addition, the Manager, Quality Operations will serve as the key liaison with external partners, including CMOs, and vendors, fostering strong relationships to ensure seamless quality operations across the board. This role requires a strategic thinker and a hands-on leader, responsible for ensuring compliance with all relevant policies and procedures while working closely with internal teams to drive quality excellence.