Quality Control Specialist Kiniksa PharmaceuticalQuality Control SpecialistLexington, MAResponsibilities (including, but not limited to): Oversee systems supporting GMP stability programs including tracking and trending of stability data, generation of protocols and reports, and driving timely completion of quality records. Standout Skills for Impact: Proven ability to manage projects and work with cross-functional teams comprised of internal and/or external contacts, including CTLs.
Quality Control Specialist Kiniksa Pharmaceuticals CorpQuality Control SpecialistLexington, MA$72,000–$91,500 / yearWith deep expertise in immunology and inflammation, Kiniksa is advancing a growing portfolio of approved and investigational medicines, anchored by its lead product, ARCALYST, the first and only FDA‑approved therapy for recurrent pericarditis. Responsibilities (including, but not limited to): Oversee systems supporting GMP stability programs including tracking and trending of stability data, generation of protocols and reports, and driving timely completion of quality records.
Quality Control Technician PhilipsQuality Control TechnicianBedford, MA$27.46–$43.94 / hourYou're the right fit if: You have a minimum of 2+ years experience in FDA/ISO 13485 regulated Medical Device manufacturing quality environments, with a focus on production controls, supporting validations, administering calibration, quality records, incoming/in-process/final Inspection, using hand tools and optical inspection systems. The Quality Control Technician is responsible for supporting highly complex quality control tasks to address manufacturing abnormalities, and coordinates quality control protocols while ensuring adherence to Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
Analyst II, Quality Control Molecular Biology The Steely GroupAnalyst II, Quality Control Molecular BiologyWoburn, MAThe QC Analyst II will perform analytical methods including but not limited GC titer determination by ddPCR and qPCR, impurity testing, and other methods as needed to support in-process, drug substance and drug product release, stability to support AAV-based gene therapy programs. Routine work includes release and stability testing, critical reagent qualification, method validation and transfer, critical reagent qualification, analyzing data, and authoring technical documents.
Quality Control Co-op Beam Therapeutics IncQuality Control Co-opCambridge, MA$23–$34 / hourBeam's suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA. This role is intended to support PLI readiness, method lifecycle activities, laboratory organization, reagent traceability, and quality-system-related activities while providing hands-on exposure to a GMP-regulated laboratory environment.
Quality Control Technician North Coast SeafoodsQuality Control TechnicianBoston, MAThe QC Technician will participate in the inspection and grading of Grade-A products, perform moisture analysis, produce written reports, verify inventory, quality, and usability of products. They will test products across three stages of production (before, in-process, and final) to ensure that the final product is safe to release for sale or distribution and report findings back to management.
Quality Control Technician II amrizeQuality Control Technician IISaugus, 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.
Senior Director, Analytical Development & Quality Control Rhythm Pharmaceuticals IncSenior Director, Analytical Development & Quality ControlBoston, MA$210,000–$370,000 / yearYou will lead and develop a high-performing organization while overseeing external partners, including CDMOs, CROs, and contract laboratories, to deliver analytical development and QC activities across drug substance and drug product. As the Senior Director, Analytical Development and Quality Control, you will provide strategic and technical leadership for analytical development and quality control across Rhythm's portfolio, spanning discovery through commercialization and lifecycle management.
NewSenior Director, Quality Control Stoke Therapeutics IncSenior Director, Quality ControlBedford, MA$235,000–$260,000 / yearThis person is accountable for the end-to-end QC strategy, including analytical control and stability strategy, oversight of external QC operations, and regulatory readiness for early clinical development through late-stage development and commercialization. The ideal candidate is a seasoned QC leader with expertise in analytical method lifecycle management, can demonstrate the ability to successfully work with CMOs and CTLs, and a proven ability to build scalable, phase appropriate processes in a lean environment.
Supervisor Quality Control, Analytical Laboratory Integra LifeSciencesSupervisor Quality Control, Analytical LaboratoryMassachusettsOversee and coordinate analytical testing of raw materials, in-process materials, finished products, validation samples, stability samples, and special studies in support of manufacturing operations and product release. Ensures compliant laboratory operations, data integrity, testing execution, inventory control, personnel development, and inspection readiness while partnering with Manufacturing, QA, Engineering, Product Development, and external laboratories.
Senior Quality Control Analyst I - Data Review TandymSenior Quality Control Analyst I - Data ReviewWoburn, Massachusetts$40–$50 / hourThis position supports gene therapy quality control activities by reviewing analytical data, ensuring compliance, and helping maintain the integrity and timeliness of product release decisions. Experience supporting deviations, investigations, CAPAs, OOS, OOTs, change controls, audits, inspections, SOPs, or procedure updates.
Associate Director, Quality Control (56861) Praxis Precision MedicinesAssociate Director, Quality Control (56861)Boston, MAPraxis is seeking a highly experienced, motivated, and innovative quality leader with strong experience in late-stage development and commercialization to join our Quality team as Associate Director, Quality Control to support QC product release and stability activities. Reporting to Senior Director, Quality Operations CMC, this position will be responsible for managing and executing Quality Control activities in support of product testing, release, and stability, and toxicology studies test material inventory support.
Data Review Specialist, Quality Control Ocular Therapeutix IncData 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.
NewQuality Control Analyst II Alnylam Pharmaceuticals IncQuality Control Analyst IICambridge, MAKey Responsibilities (including but not limited to): Perform routine and non-routine analytical, preferably HPLC/UPLC and/or microbiological assays to support raw materials, in-process samples, product release, and stability studies, following established SOPs. Qualifications: B.S. in chemistry, biology, or biochemistry, or related scientific field; Pharmaceutical/Biotech industry experience with 4-8 years in a GMP Quality Control function or equivalent, relevant industry experience.
Quality Control Analyst I - Microbiology Catalent Pharma Solutions, Inc.Quality Control Analyst I - MicrobiologyChelsea, MA$59,000–$75,000 / yearConducts collection and testing of utilities such as USP water, clean steam, CDA and Nitrogen; Perform Microbial Enumeration testing on final product release samples; Ability to isolate and sub-culture microorganisms for identification. Important Security Notice to U.S. Job Seekers: Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media.
Manager, Quality Control Vertex Pharmaceuticals IncManager, Quality ControlBoston, MA$117,800–$176,800 / yearGeneral Summary: The Manager, Quality Control is a key position that provides oversight of a variety of analytical functions that occur across the Vertex Manufacturing Center (VMC) and Leiden Center (LC1) supporting testing, and reporting of in-process, release, and stability samples. We seek talent who bring an external perspective, demonstrate curiosity and sound judgment, and thoughtfully adopt new capabilities that improve decision-making, drive innovation, increase efficiency, and help deliver better outcomes for patients.
Quality Control Manager S&R CorporationQuality Control ManagerLowell, MAFull timeengineering degree (or higher) OR 5+ additional years of management or materials testing experience in highway bridge constructionExperience working on design-build or accelerated construction projectsAbility to read plans and perform quantity take-offsProficiency in Microsoft 365 applications and Bluebeam softwareIn-depth knowledge of building codes, construction methods, materials, regulations, and quality control processesStrong leadership skillsAnalytical problem-solving skills and decision-making abilitiesCommunication skills with the ability to effectively work with stakeholders at all levelsOrganizational skills for multitaskingAbility to work on active construction sites in all weather conditionsBonus QualificationsProfessional quality control or construction management certifications (ISO 9001, ASQ CQE, etc.)Proficiency in construction project management tools like ProjectSight or SpectrumWHY YOU SHOULD JOIN USFounded in 1987 by brothers Steven and Roger Ploof, S&R Corporation has grown from a small demolition business into a leading general contractor specializing in demolition, construction, and environmental services for both public and private sectors. This is a highly collaborative and dynamic role where you'll coordinate with project managers, superintendents, and subcontractors to deliver safe, compliant, and high-quality results that meet (and exceed) the client's expectations.
Environmental Monitoring Associate - Quality Control TandymEnvironmental Monitoring Associate - Quality ControlBedford, Massachusetts$32 / hourThis role supports controlled manufacturing operations by performing environmental monitoring, utility sampling, documentation, and microbial enumeration in a GMP-regulated setting. Perform environmental monitoring tasks for aseptic and controlled areas, as well as plant utility systems, following SOPs and GMP documentation.
Associate Director, Analytical Development and Quality Control Small Molecules Zenas BioPharma (USA) LLCAssociate Director, Analytical Development and Quality Control Small MoleculesWaltham, MA$161,400–$201,842 / yearZenas' earlier stage programs include ZB021, a clinical-stage, potentially best-in-class, oral, IL-17AA/AF inhibitor; ZB022, a preclinical, potentially best-in-class, oral, brain-penetrant, TYK2 inhibitor; and ZB014, a preclinical half-life extended anti-CD-19 and FcRIIb monoclonal antibody. Our core business strategy combines our experienced leadership team with a disciplined product candidate acquisition approach to identify, acquire and develop product candidates globally that we believe can provide superior clinical benefits to patients living with autoimmune diseases.
Director, Analytical Development and Quality Control Biologics Zenas BioPharma (USA) LLCDirector, Analytical Development and Quality Control BiologicsWaltham, MA$176,900–$221,219 / yearZenas' earlier stage programs include ZB021, a clinical-stage, potentially best-in-class, oral, IL-17AA/AF inhibitor; ZB022, a preclinical, potentially best-in-class, oral, brain-penetrant, TYK2 inhibitor; and ZB014, a preclinical half-life extended anti-CD-19 and FcRIIb monoclonal antibody. Serve as a subject matter expert on key technical aspects of cell-based assay development, including protein conjugation, antibody screening, assay diluent formulation, preanalytical sample processing, scale-up, assay optimization, troubleshooting, data analysis, and analytical method validation.