Data Review Specialist, Quality Control Ocular TherapeutixData Review Specialist, Quality ControlBedford, MA$98,000–$113,000 / yearPosition Summary: The Data Review Specialist will apply strong technical knowledge of laboratory operations, analytical data review, data integrity requirements, and quality systems to perform thorough reviews of analytical chemistry, microbiology, stability, and release testing data for accuracy, completeness, scientific soundness, and compliance with cGMP, GLP, and ALCOA+ expectations. In addition to data review, this role will support QC data monitoring activities, including evaluation of release data, raw material testing data, and stability data trends to identify emerging patterns, atypical results, potential OOT signals, and opportunities for improved product understanding.
Document Control Specialist, Quality The Steely GroupDocument Control Specialist, QualityBedford, MAThis role will work closely with members of the Document Control team and support routine daily operations for Document Management. This position will primarily be responsible for the processing and maintaining of GxP documents throughout their lifecycle with a focus on issuance and reconciliation.
NewData Integrity Program Manager - Quality Control Rentschler BiopharmaData Integrity Program Manager - Quality ControlMilford, Massachusetts$120,000–$150,000 / yearThe QC Data Integrity Program Manager, will be responsible for ensuring compliance and alignment to all relevant regulatory and internal requirements related to data integrity as well as developing training material and leading training efforts with Quality Control Staff. As a German family-owned company with an international footprint and global reach, we combine experts, expertise and years of experience to develop best-in-class solutions – together with our clients.
Associate II, Quality Control Moderna IncAssociate II, Quality ControlMarlborough, MA$63,200–$100,900 / 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 Individual will support cGMP microbiology methods for QC raw material, plasmid, drug substance, Stability, finished product testing for mRNA products produced and Environmental and critical utilities monitoring at Moderna's manufacturing facility.
Director, Quality Control Editas Medicine IncDirector, Quality ControlCambridge, MAThe successful candidate will collaborate with a high-performing CMC team, coordinating with process and analytical experts cross-functionally in Research and Discovery, Process Development, Analytical Sciences, Manufacturing, and Quality Assurance, to transfer, qualify and oversee in-process and release testing to advance Editas' in vivo gene medicine portfolio. Characterizing Your Impact: As the Director, Quality Control, you will: Lead phase appropriate CMC analytical development, qualification/validation, transfer and optimization through strong collaboration with key stakeholders and external partners.
Quality Control Analyst I, Raw Materials Ocular TherapeutixQuality Control Analyst I, Raw MaterialsBedford, MA$68,000–$75,000 / yearOcular 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. Key Responsibilities: The primary responsibilities of this role will be performing qualitative and quantitative testing of raw materials using techniques such as HPLC, GC, FTIR, UV-Vis, titration, and wet chemistry.
Quality Control Technician II Amrize LtdQuality Control Technician IISaugus, MAWHAT WE'RE LOOKING FOR Education: High school diploma or equivalent Additional Education Preferred: Associates degree Required Work Experience: 3-5 year Required Training/Certifications: State regulated or industry certifications, as required Additional Requirements: Ability to work various hours including weekends and nights. Detailed oriented Able to prioritize work Valid Driver's License, Clean Driving Record Successful candidates must adhere to all safety protocols and proper use of Amrize approved Personal Protection Equipment, including but not limited to respirators.
Quality Control Lab Tech Amrize LtdQuality Control Lab TechRockland, MAWe're seeking a Quality Control Lab Tech who's ready to be part of a company committed to formulating everyday success for every customer through innovative, reliable products used to adhere, seal, and protect at every level of the building envelope. Personal ability to be comfortable in the Quality role knowing that you are responsible for presenting accurate data and are not authorized to make decisions on the disposition of nonconforming product.
Quality Control Technician II 1 Amrize LtdQuality Control Technician II 1Wrentham, MASubject to applicable law, employees that are required to wear respirators must be clean shaven where the respirator seal meets the face in order to pass the qualitative and quantitative fit tests. Maintains mix designs as required by DOT or local city/county specifications or to ensure accuracy of products used in mix.
NewQuality Control Analyst (Contract) 651 Vertex PharmaceuticalsQuality Control Analyst (Contract) 651Boston, Massachusetts$38–$45 / 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: Within our Analytical Service team, we have a functional service provider solution, which is a unique partnership that allows our customers to leverage the experience of our staff, while allowing you, the employee, to gain direct experience working onsite at a pharmaceutical/ biopharmaceutical company, all while maintaining full-time benefits.
Quality Control Analyst (Sun-Wed Shift) Sarepta Therapeutics Inc.Quality Control Analyst (Sun-Wed Shift)Andover, MA$78,400–$98,000 / yearThe successful candidate will have hands-on experience with cell-based in-vitro potency assays, cell culture, SDS-PAGE, western blot, Automated Western blot assays, enzyme activity measurements, protein extraction, purification, and quantification methods. The successful candidate will work within the QC team, testing gene therapy products utilizing cell-based assays (Potency assay) in support of clinical and commercial lot release and stability activities.
Quality Control (Metrology Lab/Med device Night Shift & 2nd) SmcQuality Control (Metrology Lab/Med device Night Shift & 2nd)MassachusettsThis position has primary responsibilities which include accurate part and assembly inspections and tests performed to customer specifications, operating computerized inspection systems, such as coordinate measurement machines and vision inspection equipment. Comprised of dedicated people and decades of manufacturing experience, we have continued to experience strong growth and currently have outstanding career opportunities for equally dedicated people.
Principal Business Consultant - Quality Control Veeva Systems IncPrincipal Business Consultant - Quality ControlBoston, MA$120,000–$250,000 / yearYou will focus on transforming our customer's laboratory network with Veeva's disruptive LIMS software, including reshaping operating models, driving organizational change, and measuring tangible business value. As a Principal Business Consultant focused on Quality Control in our Quality Practice, you will help customers bring treatments to patients faster by transforming how they work with Technology, Data, and AI.
Quality Control Manager (Traveling) Consigli Construction Co IncQuality Control Manager (Traveling)Milford, MADocumentation and Reporting: Maintain detailed documentation of inspection findings, including photographs, data sheets, and non-conformance reports, and generate regular quality reports for project management. Quality Control Planning: Develop and implement comprehensive quality control plans aligned with project requirements, including inspection checklists, sampling procedures, and testing protocols.
Quality Control Analyst (Sun-Wed shift) Sarepta Therapeutics IncQuality Control Analyst (Sun-Wed shift)Andover, MA$78,400–$98,000 / yearThe successful candidate will have hands-on experience with cell-based in-vitro potency assays, cell culture, SDS-PAGE, western blot, Automated Western blot assays, enzyme activity measurements, protein extraction, purification, and quantification methods. The successful candidate will work within the QC team, testing gene therapy products utilizing cell-based assays (Potency assay) in support of clinical and commercial lot release and stability activities.
Quality Control Technician Amrize LtdQuality Control TechnicianMASubject to applicable law, employees that are required to wear respirators must be clean shaven where the respirator seal meets the face in order to pass the qualitative and quantitative fit tests. Additional Requirements: Successful candidates must adhere to all safety protocols and proper use of Amrize approved Personal Protection Equipment ("PPE"), including but not limited to respirators.
Associate Director, Analytical Development & Quality Control Alpha-9 Oncology IncAssociate Director, Analytical Development & Quality ControlBoston, MAThe successful candidate will manage relationships with external manufacturing and testing partners while partnering closely with Quality, Regulatory, Technical Operations, and Program Leadership teams to support API development, CMC activities, and timely execution of clinical supply strategies. Alpha-9 Oncology is seeking a highly experienced and motivated Associate Director, Analytical Development & Quality Control, to provide technical and operational leadership for QC activities supporting our clinical-stage radiopharmaceutical programs.
Quality Control Systems Manager CharterQuality Control Systems ManagerMassachusettsDocumentation & Reporting Prepare and maintain required QC documentation, including daily QC reports, test results, deficiency logs, and meeting minutes. Types of work include environmental remediation, demolition, excavation, dredging, utility work, and landfill cap/closure projects.
Quality Control Analyst II, Release & Stability Testing (3rd Shift - Contract) Rentschler BiopharmaQuality Control Analyst II, Release & Stability Testing (3rd Shift - Contract)Milford, Massachusetts$39–$46 / hourThe Quality Control Analyst II, Release and Stability Testing is responsible for the cGMP analytical testing of stability samples and evaluation of data to ensure compliance with analytical methods, stability protocols, client criteria, Good Laboratory Practices (GLP) and Good Manufacturing Practices (cGMP). SME to support or lead activities related to OOS/OOT investigations, deviations, change controls, corrective actions, and preventive actions to correct and eliminate the potential for non-conformances.
Quality Control Data Reviewer Rentschler BiopharmaQuality Control Data ReviewerMilford, MassachusettsAs part of the Milford site’s Quality Control team, the Data Reviewer is responsible for the cGMP analytical data review and documentation generated during laboratory analysis in the quality control laboratory. Actual compensation is determined based on several factors that may include seniority, education, training, relevant experience, relevant certifications, geography of work location, job responsibilities, or other application factors permissible by law.