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).
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).
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...
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.
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.
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.
Quality Control Analyst- Gas Operations EversourceQuality Control Analyst- Gas OperationsSouthborough, MA$95,600–$106,220 / yearRole 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.
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.
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.
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.
Sr. Quality Specialist, Gxp Document Control Bicara Therapeutics IncSr. Quality Specialist, Gxp Document ControlBoston, MAFICERA 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.
Director, Quality Control Editas MedicineDirector, Quality ControlCambridge, MA$215,000–$235,000 / yearThe 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. The Quality team is seeking a highly motivated and experienced technical and organizational leader in gRNA, mRNA, and Lipid Nanoparticle (LNP) analytical methodologies and GMP testing.
Senior Director, Biologics Analytical Development and Quality Control Korsana BiosciencesSenior Director, Biologics Analytical Development and Quality ControlBoston, MassachusettsThis leader will oversee the planning and execution of outsourced analytical development and testing activities and will work proactively with external suppliers including CDMOs and contract labs to define project scope, mitigate risks, and ensure successful delivery in relation to technical quality, timelines and budget. Collaborates with internal stakeholders in the areas of Drug Substance Development, Drug Product Development, Combination Product Development, Clinical Supply Chain, Program Management, Preclinical Development, Clinical Development/Operations, Quality, Regulatory Affairs, and external business partners to push project forward.
Component Quality Control Technician Rhode Island Blood CenterComponent Quality Control TechnicianProvidence, Rhode IslandFull timeOverview: Founded in 1979, Rhode Island Blood Center (RIBC) has served Rhode Island and the New England area for more than 45 years, delivering more than 90,000 lifesaving blood products annually to 50+ hospitals, EMS and healthcare partners. Kimball Research Institute is a leader in hematology and transfusion medicine research, dedicated to the study, prevention, treatment and cure of bloodborne and blood-related diseases.
Staff Design Control Engineer, Design Quality (IVD/CDx/Medical Device)) Quest Diagnostics IncStaff Design Control Engineer, Design Quality (IVD/CDx/Medical Device))Marlborough, MA$105,000–$125,000 / yearThe Staff Design Quality Engineer is a highly experienced technical quality leader responsible for quality oversight of complex IVD medical device development programs, high-risk changes, and technically demanding validation and design transfer activities. Provide authoritative review and approval of key design control deliverables, including design and development plans, requirements, risk files, validation strategies, design reviews, traceability matrices, and transfer packages within delegated authority.
Scientist I, Quality Control Replimune Group IncScientist I, Quality ControlFramingham, MAThe 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).