Director, Quality Control Contractor Centessa Pharmaceuticals PlcDirector, Quality Control ContractorBoston, MA$95–$120 / hourThe Director, Quality Control (contractor) will provide leadership and oversight for analytical testing, stability programs, specification management, and quality control activities supporting clinical and commercial development. Contractors engaged through Centessa are employed through a third-party agency that serves as the employer of record and provides access to a comprehensive benefits package.
Quality Control Technician- Acushnet CRH AmericasQuality Control Technician- AcushnetCranston, RI$23–$25 / hourOur modern facilities, veteran paving crews, experienced construction management team and large investment in plants and equipment make us one of the largest and most efficient producers in the state of Massachusetts as well as one of only two RIDOT approved stone suppliers in the state of Rhode Island. Responsible for collecting, measuring and testing of materials for construction projects including hot mix asphalt, soils sampling, aggregate sampling, core sampling, nuclear density testing, laboratory testing and mix design.
Quality Control Analyst II Anika Therapeutics IncQuality Control Analyst IIWestborough, MAnClick the button below to submit your application for this position.\n \nApply Now\n \nOther Open Positions\n \nCareer\n \nShift Lead Aseptic Manufacturing\n \nFull-Time\u2022Bedford, MA\n \nWhat You'll Do The Shift Lead Aseptic Manufacturing leads day-to-day aseptic manufacturing floor operations for sterile drug and medical device products produced within ISO 5\u2026\n \nView Position\n \nCareer\n \nSenior Warehouse Specialist\n \nFull-Time\u2022Bedford, MA\n \nWhat You'll Do The Senior Warehouse Specialist plays a crucial lead role in managing complex warehouse operations, including domestic and international shipments, inventory control, and\u2026\n \nView Position\n \nCareer\n \nQuality Control Microbiologist\n \nFull-Time\u2022Bedford, MA\n \nWhat You'll Do The QC Microbiologist performs microbiological testing and validation activities supporting commercial manufacturing operations under GMP conditions, ensuring compliance with regulatory requirements, product\u2026\n \nView Position\n \nProducts Navigation" data-detect-dark-bg="true">Products\n\n Regenerative Solutions\n OA Pain Management\n Our Technology\n \nResources Navigation" data-detect-dark-bg="true">Resources\n\n Literature & Videos\n News & Blog\n Just For Patients\n Events\n Certifications\n Form 1095-C\n Instructions for Use\n Find a Doctor\n \nCompany Navigation" data-detect-dark-bg="true">Company\n\n About Anika\n Meet Our Team\n Our Story\n Join Us\n \nConnect Navigation" data-detect-dark-bg="true">Connect\n\n Investor Relations\n Contact Us\n Find a Rep\n \nFollow Us\n\n LinkedIn\n Instagram\n Facebook\n X\n* YouTube\n \n3 Media Web Solutions, Inc\n \n2026 Anika Therapeutics, Inc. In this role, you develop subject matter expertise in analytical testing methodologies, laboratory instrumentation, and quality control systems within regulated pharmaceutical and medical device environments.\n \nHow You'll Contribute\n\n Perform analytical testing of incoming raw materials according to USP, EP, ACS Reagent Index, and approved internal methods.\n
Quality Control Analyst LanceSoft IncQuality Control AnalystLexington, MA$34–$37.29 / hourJob 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.
Quality Control Analyst II, Release & Stability Testing (3rd Shift - Contract) Rentschler BiopharmaQuality Control Analyst II, Release & Stability Testing (3rd Shift - Contract)Milford, MassachusettsThe 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.
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.
NewAssociate Director, Analytical Development & Quality Control Entrada Therapeutics IncAssociate Director, Analytical Development & Quality ControlBoston, MARemote$172,000–$202,000 / yearWe are a tight-knit team of experts and leaders in both therapeutic development and rare diseases and are excited to grow and attract colleagues who are ready to join a high-energy, dedicated team that likes to get things done and dramatically improve the lives of patients and their families. We expect multiple clinical data readouts as we advance several DMD programs across the U.K., EU, and U.S. By year-end 2026, we anticipate four clinical-stage programs in our DMD franchise (ENTR-601-44, ENTR-601-45, ENTR-601-50, and ENTR-601-51).
Director, Quality Control Dyne TherapeuticsDirector, Quality ControlWaltham, MA$190,000–$230,000 / yearThe Director, Quality Control leads global Quality Control activities, including oversight of external laboratories supporting analytical testing, release, and stability programs across clinical and commercial stages. Regulatory, Inspection Readiness & Cross-Functional Collaboration Prepares and reviews analytical CMC content for regulatory submissions (INDs, BLAs) and supports interactions with global health authorities.
Quality Controller (Manufacturing) MOOQuality Controller (Manufacturing)East Providence, RIDiversity Statement We are working hard to create a representative, inclusive and super-friendly team, because we know that different experiences, perspectives and backgrounds make for a better workplace. And we are committed to continuous investment in building an open and inclusive environment, welcoming a diverse audience of candidates who see themselves working and thriving at MOO.
NewDirector, Quality Control (contractor) Centessa Pharmaceuticals, a wholly owned subsidiary of Eli Lilly and CompanyDirector, Quality Control (contractor)Boston, MA$95–$120 / hourCentessa Pharmaceuticals, a wholly owned subsidiary of Eli Lilly and Company, is a clinical-stage company developing orexin receptor 2 (OX2R) agonists as a new class of medicines for the treatment of narcolepsy and potentially other sleep-wake disorders. Centessa’s lead investigational candidate – cleminorexton (formerly ORX7...
Scientist I, Quality Control ReplimuneScientist I, Quality ControlFramingham, MassachusettsThe 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. The QC Analytical Scientist will be required to assist with scheduling, performing and reviewing of tests results of raw materials, in-process, drug substance and final drug product samples following established test method (SOPs).
Quality Control Analyst II BioPharma Consulting JAD GroupQuality Control Analyst IINorton, MAThe role includes performing routine and non-routine testing, participating in data trending, investigations, and lab operations, and supporting method transfers, qualification/validation, verification, and implementation. Perform routine/non-routine analytical (HPLC/UPLC) and/or microbiological assays for raw materials, in-process samples, product release, and stability studies following SOPs.
Quality Control Scientist II LancesoftQuality Control Scientist IIWestborough, MA$50Manufacturing by ensuring effective microbiological testing, mentoring laboratory staff, supporting quality systems and delivering aseptic technique training to maintain. Track and support quality system activities including deviations, investigations, CAPAs, Change Control and trending associated with QC microbiology operations.
Senior Quality Control Analyst Actalent IncSenior Quality Control AnalystNorwood, MA$34–$39 / hourThe ideal candidate will have experience in molecular biology techniques, mammalian cell culture, potency assays, and QC testing within a pharmaceutical, biotechnology, or life sciences setting. 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.
Scientist, Quality Control Analytical Development (6-month Contract) Rentschler BiopharmaScientist, Quality Control Analytical Development (6-month Contract)Milford, Massachusetts$45–$55 / hourPrimary focus on the execution of experiments to support the validation of molecular biology assays including but not limited to ELISAs for residual HCP, residual protein a, and relative potency assays as well as qPCR. Experience in other biophysical characterization methods CE (capillary electrophoresis), chromatography, SEC/RP/IEX-U(H)PLC, SDS-CGE, iCIEF, CIEX, Peptide mapping is a plus.
Claims Quality Control Auditor (44912) Neighborhood Health Plan of Rhode IslandClaims Quality Control Auditor (44912)Smithfield, RIResponsibilities include, but are not limited to the following: Review Neighborhood's claim process functions, including auto adjudicated and manually processed claims and issues, based on provider and health plan contractual agreements and claims processing guidelines. This Master IA will be created from results of the weekly Claims Adjustment Committee meeting and be used by adjusters from each delegate to reprocess claims according to the respective configuration changes in each system.
NewQuality Control Analyst I - Microbiology CatalentQuality Control Analyst I - MicrobiologyChelsea, MassachusettsConducts 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.
NewQuality Control Analyst I - Microbiology Catalent IncQuality 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.
Document Control Manager - Quality, Compliance, and Oversight Massachusetts Bay Transportation AuthorityDocument Control Manager - Quality, Compliance, and OversightBoston, MAHave a satisfactory work record for the two (2) years immediately prior to the closing date of this posting (unless if current student or recent graduate), including overall employment, job performance, discipline, and safety records (infractions and/or offenses occurring after the closing of the posting and before the filling of a vacancy may preclude a candidate from consideration for selection). Bachelor's degree from an accredited institution in Business Administration, Engineering, Information Technology, Computer Science or a related field with 5 or more years of professional experience in business administration, library management, document management, information technology, training management or related field.