Cgmp Jobs

Lead global drug product development and CDMO operations at Dyne Therapeutics to ensure reliable clinical supply and commercial launch readiness for injectable therapeutics.

Customer-Centric

Mission Driven

Inclusive & Diverse

Work/Life Harmony

Bluesight is hiring a Senior Security Infrastructure Engineer to lead cloud security, threat detection, and compliance automation across its AWS-based healthcare SaaS environment.

Support AbbVie's Worcester manufacturing operations as an Automation Engineer responsible for PLC/HMI/SCADA development, commissioning, validation and ongoing troubleshooting in a cGMP environment.

Bristol Myers Squibb is hiring a Manager of Operational Excellence at its Devens cell therapy site to drive lean transformation, capacity modeling, and measurable process improvements across operations and supply chain.

An early-stage herbal wellness brand seeks a Quality & Compliance Specialist to own cGMP-driven QA systems, certification management, and regulatory review across a growing dietary supplement portfolio.

AbbVie is hiring an onsite Quality Validation Specialist in North Chicago to lead and approve validation activities, drive investigations/CAPAs, and maintain validated status for equipment, systems and processes.

AbbVie seeks a Laboratory Technician II (3rd Shift) to perform analytical testing, maintain lab equipment, and support GMP-compliant operations at its Barceloneta, Puerto Rico facility.

Support QC laboratory operations on the overnight shift by verifying, handling, organizing, and delivering samples while maintaining regulatory and environmental monitoring standards.

Vertex is hiring a hybrid contract Project Manager with CDMO and tech-transfer experience to lead cross-functional CMC projects supporting cell and gene therapy development.

Supervise and lead a second-shift Quality Assurance team at AbbVie's Barceloneta manufacturing site to ensure GMP compliance, product quality, and on-time batch release.

Experienced QA leader sought to manage GMP quality systems, audits, and staff for a 3–6 month contract at a global CRDMO, with potential for full-time conversion.

Pfizer is hiring a QA Manager, Investigation Review to lead complex cGXP investigations, drive quality improvements, and represent QA across cross-functional teams at the Sanford, NC facility.

Quality Manager sought to lead site QA and maintain regulatory and customer compliance for a regulated manufacturing operation in Mayfield, KY.

Experienced analytical science SME needed to lead development, validation, and network implementation of rapid microbiology safety methods for Vertex’s biologics and cell & gene therapy commercial programs on a 24-month part-time contract.

Dental Insurance

Disability Insurance

Vision Insurance

Equity

Paid Time-Off

Medical Insurance

Mental Health Resources

Paid Holidays

Company Retreats

Hims & Hers is hiring an onsite Night Shift Quality Control Supervisor for its Gilbert non-sterile compounding pharmacy to lead inspections, support compliance, and coach QC staff.

Hovione seeks an Associate Process Engineer to support cGMP pharmaceutical manufacturing, process documentation, and technical improvements at its East Windsor site.

Catalent's Kansas City facility is hiring a Document Control Coordinator II to manage GMP controlled-document workflows, ensure compliance with SOPs/cGMP, and support quality systems onsite.

Cellares is hiring a Senior Director, IDMO Site Quality to lead QA and QC for its Bridgewater cGMP cell therapy manufacturing site, driving quality systems, regulatory compliance, and team development.

Turner & Townsend is hiring a Senior Construction Estimator (Mechanical & Process Piping) to lead cost planning and estimating for large life-science construction programs.

RRD is hiring a Packaging Technical Services Specialist to diagnose production issues, run product trials, and support clients and internal operations for folding carton and packaging projects.

Lead the Material Review Board at BMS Devens to evaluate non-conforming cell therapy material, coordinate cross-functional risk assessments, and deliver disposition options that enable safe patient treatment.

Experienced analytical chemist needed to lead HPLC method development, validation and GMP testing for Eurofins BioPharma in Lancaster, PA.

At Elanco's Winslow manufacturing site, the Quality Assurance Associate will ensure product and process quality by managing deviations, supporting batch disposition, and driving compliance across operations.

Bristol Myers Squibb seeks a Specialist, Investigations to lead deviation investigations and CAPA activities within its cGMP cell therapy manufacturing site in Devens, MA.

Orca Bio is hiring a 2nd-shift Supervisor, Clinical Manufacturing to oversee on-site cell therapy production in Sacramento, ensuring quality, compliance, and efficient shift operations.

Lead and mentor a second-shift QC laboratory team at AbbVie's Barceloneta site, ensuring accurate analytical testing, cGMP compliance, and timely product release.

Lead technical strategy and execution for cell line development and tech transfer, delivering robust CLD and upstream process transfers to pharmaceutical and biotech partners from Asimov’s Boston site.

CRB is hiring an experienced Process Engineer III/IV with deep small-molecule manufacturing and process design expertise to lead client-facing projects, scale-up efforts, and cross-discipline engineering teams.

CRB is hiring a Senior Lead Process Engineer (OSD focus) to lead technical strategy, design oversight, and regulatory-aligned process solutions for complex oral solid dosage projects.

Eurofins Scientific is hiring a Lab Operations Support - Instrumentation in Malvern, PA to oversee instrument maintenance, sample logistics, and cGMP lab operations.

Cresilon is seeking an experienced R&D Formulation Manager/Principal Scientist to lead polymer formulation and materials development for life‑saving hydrogel hemostatic devices in Brooklyn, NY.

QRC Group is hiring a CSV Specialist with bioprocess validation expertise to execute commissioning, qualification and computerized system validation across manufacturing and laboratory environments.

Senior Scientist role at Eurofins USA Medical Devices focused on PFAS testing and method development, requiring hands-on chromatography experience and cGMP/ISO lab familiarity.

Eurofins seeks an experienced Laboratory Supervisor to lead microbiology operations at its Lancaster, PA facility, overseeing staff, quality systems, and client-facing activities.

Dental Insurance

Disability Insurance

Vision Insurance

Equity

Paid Time-Off

Medical Insurance

Mental Health Resources

Paid Holidays

Company Retreats

Hims & Hers is hiring a Quality Systems Lot Disposition Specialist to oversee batch record review, lot disposition, and quality documentation for XeCare Pharmacy to ensure compliance with regulatory and company standards.

Operational Quality Document and Training Specialist needed to manage controlled documents, ensure cGMP/GDP compliance, and deliver document-control training within Vertex's QMS.

Lead and scale technical operations for a mission-driven clinical-stage veterinary biotech, overseeing manufacturing, formulation, analytical development, and CDMO partnerships from discovery to commercial launch.

Dental Insurance

Disability Insurance

Vision Insurance

Equity

Paid Time-Off

Medical Insurance

Mental Health Resources

Paid Holidays

Company Retreats

Hims & Hers seeks a hands-on Quality Control Supervisor to ensure product quality, regulatory compliance, and team coaching at our New Albany non-sterile compounding facility.

Grove Collaborative is hiring a Senior Quality & Regulatory Manager to own quality systems and regulatory compliance for Grove Co. owned brands, spanning supplements, home, and personal care products.

Lead and scale Serán BioScience's commercial manufacturing operations to ensure on-time, compliant delivery of client projects while advancing commercial strategy and customer relationships.

Eurofins Scientific is hiring a Pharmaceutical QA Senior Specialist - Group Leader to lead QA oversight for QC operations, ensuring cGMP compliance and robust release-ready documentation at the Sanford site.

Lead critical cGMP manufacturing operations for Biogen's large-scale cell culture team by executing processes, coaching associates, and ensuring high-quality documentation and compliance.

Dental Insurance

Disability Insurance

Vision Insurance

Equity

Paid Time-Off

Medical Insurance

Mental Health Resources

Paid Holidays

Company Retreats

Join Hims & Hers as a Pharmaceutical Validation Engineer to lead CQV and IQ/OQ/PQ validation for sterile and non-sterile compounding facilities and ensure regulatory compliance.

QRC Group is hiring a bilingual Quality Systems Documentation Specialist to manage and maintain regulatory documentation and support validation activities at its Vega Baja, PR location.

Lead the onsite maintenance organization at AbbVie’s Irvine facility to ensure reliable, compliant utilities and equipment through strong technical leadership and continuous improvement.

AbbVie is hiring a Process Engineering Lead in Irvine to oversee facilities and calibration operations, lead process engineering projects, and ensure cGMP-compliant equipment reliability.

Catalent is hiring an on-site Associate Scientist in Winchester, KY to support analytical method development, validation, and routine release/stability testing for clinical and registration programs.

Experienced analytical instrumentation specialist needed to lead validation, qualification, and method transfers for QC instruments in a regulated life-sciences environment.

Lead AbbVie's third‑party aseptic manufacturing partnerships to ensure compliant, on‑time production and continuous performance improvement across TPMs.

Lead multi-site warehouse operations at AbbVie’s Barceloneta facility, driving inventory accuracy, regulatory compliance, and operational efficiency in a regulated pharmaceutical environment.