Quality Control Analyst- GAS Operations Eversource EnergyQuality Control Analyst- GAS OperationsNew Bedford, MassachusettsRole and Scope of Position: Supports the implementation, of the Eversource Quality Control (QC) program as it relates to any of the following construction, maintenance, meter service, leak survey, corrosion, damage prevention, LNG and I&R activities at Eversource Gas. This role works in an environment that often requires the performance of multiple simultaneous activities, where deadlines need to be met and work is performed under pressure while involving significant business commitments and results.
Brand Rep - Audits, Merchandising And Quality Control - $24/Hr ThirdChannelBrand Rep - Audits, Merchandising And Quality Control - $24/HrLeominster, MAAs an independent Brand Representative, you will act as a key liaison between the brand and retail store environments, conducting recurring in-store visits to perform audits, ensure product quality, and elevate the brand experience. Through innovative in-store retail technology solutions, we bring products to life inside retail environments, helping brands optimize performance and grow in today's dynamic retail landscape.
Gas Quality Control Analyst Eversource EnergyGas Quality Control AnalystNew Bedford, MassachusettsRole and Scope of Position: Supports the implementation, of the Eversource Quality Control (QC) program as it relates to any of the following construction, maintenance, meter service, leak survey, corrosion, damage prevention, LNG and I&R activities at Eversource Gas. This role works in an environment that often requires the performance of multiple simultaneous activities, where deadlines need to be met and work is performed under pressure while involving significant business commitments and results.
NewScientist, Quality Control (QC) Systems Bristol-Myers Squibb CoScientist, Quality Control (QC) SystemsMA$107,100–$129,780 / yearBased on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day. This role acts as a subject matter expert in providing electronic systems operational support and troubleshooting to QC end users and will interface with both internal and external functions to implement electronic system improvements to optimize business processes and improve efficiency.
Change Control and Quality System Specialist Integrated Resources, IncChange Control and Quality System SpecialistLexington, MassachusettsContractorThis person will also assist with other quality system events which require regulatory CMC support (such as deviations, annual reports, inspections/audits, etc.) and act as a liaison with the Tech Ops organization. Collaborate and communicate with global CMC leads, EU and international regulatory colleagues to provide consistent, clear and timely assessments into the change control management system (50%).
Quality Control Coordinator/Cleanroom Technician (Full Time) Compass Group USA IncQuality Control Coordinator/Cleanroom Technician (Full Time)Boston, MA$25–$27 / hourWe empower and uplift each other by working together, take responsibility for doing the right thing, and believe there is no limit to our potential when we grow together across Environmental Services, Patient Transportation, Patient Observation, Facilities Management, Healthcare Technology Solutions, Ambulatory Services, and Sterile Processing. Full-time and part-time positions are offered the following benefits: Retirement Plan, Associate Shopping Program, Health and Wellness Programs, Discount Marketplace, Identify Theft Protection, Pet Insurance, and other voluntary benefits including Critical Illness Insurance, Accident Insurance, Hospital Indemnity Insurance, Legal Services, and Choice Auto and Home Program.
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.
Senior Director, Analytical Development & Quality Control Rhythm PharmaceuticalsSenior Director, Analytical Development & Quality ControlBoston, MA$210,000–$300,000 / 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.
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.
2nd Shift - Quality Control Sr. Associate/Sr. Specialist (contract) 29531` Vertex Pharmaceuticals2nd Shift - Quality Control Sr. Associate/Sr. Specialist (contract) 29531`Boston, Massachusetts$40–$44 / 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 Vertex Cell and Gene Therapy (C>) Quality Control (QC) team is responsible for the routine testing of samples and associated workflows for our internally manufactured stem-cell based T1D and genetically modified Casgevy programs.
3rd Shift - Quality Control Sr. Associate/Sr. Specialist (contract) 29622 Vertex Pharmaceuticals3rd Shift - Quality Control Sr. Associate/Sr. Specialist (contract) 29622Boston, Massachusetts$42–$52 / 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 Vertex Cell and Gene Therapy (C>) Quality Control (QC) team is responsible for the routine testing of samples and associated workflows for our internally manufactured stem-cell based T1D and genetically modified Casgevy programs.
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.
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.
Data Integrity Program Manager - Quality Control Rentschler BiopharmaData Integrity Program Manager - Quality ControlMilford, MassachusettsThe 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.
Quality Control / Documentation Analyst Katalyst Healthcares & Life SciencesQuality Control / Documentation AnalystLexington, MAJob Description: Assist in document authoring/ revision and approval (protocols, test methods, SOPs) and other routine laboratory activities supporting the lab as 079 activities are completed by the biochem team. This role supports the daily operations of the QC Raw Materials department, whose primary responsibility is the testing and release of raw materials for GMP use in manufacturing.
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.
Quality Control Analyst I RD PartnersQuality Control Analyst INorton, Massachusetts$50,469–$63,086Maintain 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. Perform routine and non-routine analytical assays to support raw materials, in-process samples, product release, and stability studies under supervision, following established SOPs.
Quality Control Analyst (Contract) 651 Vertex PharmaceuticalsQuality Control Analyst (Contract) 651Boston, Massachusetts$36–$38 / 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.
Senior Manager, Analytical Development & Quality Control Alpha-9 OncologySenior Manager, Analytical Development & Quality ControlBoston, Massachusetts$175,000–$194,000 / yearAlpha-9 Oncology is seeking a highly motivated Senior Manager, Analytical Development & Quality Control, to provide technical and operational leadership for quality control and analytical lifecycle activities across clinical-stage radiopharmaceutical programs. This role will serve as a primary analytical and QC representative supporting development programs through data trending, statistical analysis, batch release support, investigation management, CDMO oversight, analytical readiness activities, and clinical supply support.
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.