Alabama or Missouri or Illinois or Florida or Georgia or Maryland or New Jersey or Texas or Pennsylvania or Indiana or Ohio or Kentucky or Colorado or Virginia or New York or North Carolina or District of Columbia or Raleigh or Boston or Philadelphia or Chicago or Indianapolis or Columbus or St. Louis or Kansas City or Houston or Dallas or Boulder or Portland or San Francisco or San Diego or Los Angeles
FieldFull Time
PerkinElmer: Provides analytical instruments and laboratory services for scientific industries.
5+ YOEBachelor's in life sciences/engineering/regulatory (or equivalent experience); 5+ years automation/digital systems experience in GMP life sciences; strong process control/MES knowledge; willingness to travel and valid driver\u0002s license; US work authorization required.
Thermo Fisher ScientificNYSE: TMO: Sells equipment and chemicals for scientific research and healthcare.
2+ YOELead manufacturing team in formulation, ensure cGMP compliance, manage documentation and continuous improvement; 12-hour shifts; onsite in Plainville, MA.
Lean manufacturing, cGMP, Manufacturing systems, Microsoft Office
3+ YOEBachelor's degree or equivalent preferred; 3+ years of related clinical or business experience required. Supervisory, medical, cGMP, and plasma or blood experience preferred.
QA Specialist - Lot Disposition, Site Based, Redmond, WA
Redmond or Seattle or Watertown or Alderley Park or United Kingdom or United States
$90k-$100k/yrOnsiteFull Time
EvotecNASDAQ: EVO: Drug discovery and development services for life science companies.
3+ YOEBachelor's degree in biological or engineering science and 3+ years in biopharmaceutical or pharmaceutical cGMP manufacturing; requires cross-functional communication and strong analytical and organizational skills.
MannKindNASDAQ: MNKD: Develops inhaled therapeutic products for endocrine and lung diseases.
5+ YOEBS in Package Engineering with 7-10 years or MS with 5-7 years in pharmaceutical packaging; knowledge of cGMPs; packaging equipment and testing methods; strong organization and multitasking.
Senior Manager, Cell Therapy Manufacturing in Devens, MA
Devens, Massachusetts, United States
$132k-$160k/yrOnsiteFull Time
Bristol Myers SquibbNew York Stock Exchange: BMY: Develops and distributes innovative medicines for serious diseases.
8+ YOE6+ MgmtBachelor’s degree in science or engineering; 8+ years pharma experience; 6+ years in management; Lean manufacturing knowledge; cGMP experience; able to support 24/7 operations.
PCI Pharma Services: Integrated pharmaceutical development, manufacturing, and global packaging services.
2+ YOERequires 2+ years in GMP, ISO, or FDA-regulated environments, quality-system technical writing, cGMP investigations, root-cause and risk analysis; science or engineering bachelor's preferred.
Vertex PharmaceuticalsNASDAQ: VRTX: Develops and sells prescription drugs for serious genetic diseases.
4+ YOEPh.D. and 4+ years of analytical development experience, or M.S. with 7+ years or B.S. with 10+ years; small-molecule pharmaceuticals, chromatography, QbD, cGMP, and regulatory guideline knowledge required.
Quality by Design (QbD), cGMP, ICH, FDA, USP, ICH M7, chromatography
VericelNASDAQ: VCEL: Produces advanced cell therapies for sports medicine and burn care.
2+ YOEGED or equivalent and 2+ years of cGMP experience required. Requires communication, organizational, planning, teamwork, Microsoft Office, and ability to lift up to 50 pounds; cleanroom experience preferred.
QuanterixNASDAQ: QTRX: Developing digital immunoassay technology for ultra-sensitive protein detection.
8+ YOEBachelor's degree in a relevant engineering or scientific field and 8+ years in cGMP process engineering; FDA, ISO 13485, assay manufacturing, automation, troubleshooting, and statistical process expertise required or preferred.
Simoa, PhenoCycler, PhenoImager Fusion, PhenoCode Panels, Minitab, JMP, SPC, DoE, CAPA, SOPs, IQ/OQ/PQ, ISO 13485, FDA 21 CFR Part 820, cGMP
Senior Manager/Associate Director, Quality Control
Vancouver or Burnaby or Boston or Needham
$114k-$179k/yrHybridFull Time
Xenon PharmaceuticalsNASDAQ: XENE: Developing therapeutics for neurological and psychiatric disorders.
5+ YOEUndergraduate life sciences degree and 5+ years of relevant pharmaceutical management experience at Senior Manager level or 8+ years at Associate Director level; expertise in quality control, stability, investigations, and cGMP.
12+ YOE5+ MgmtRequires 12+ years relevant experience, including 5+ years leading technology deployment, automation, or tech transfer projects, with cGMP, pharmaceutical regulation, analytical technology, and cross-functional leadership expertise.
Genetix Biotherapeutics: Developing and commercializing curative gene therapies for rare diseases.
4+ YOEBachelor's degree in life sciences, engineering, or related field; 4-6 years of QA experience in GMP-regulated biopharmaceutical or cell/gene therapy manufacturing; CMO oversight experience and cGMP knowledge.
Syner-G BioPharma Group: Provides CMC and regulatory services for life sciences companies.
3+ YOEBachelor's in life science, 3+ years biotech/pharma/medical device validation experience, knowledge of FDA cGMP, FMEA, CSV, protocol generation and IQ/OQ/PQ reporting, strong written/verbal communication.
FDA cGMP, FMEA, Computerized System Validation (CSV), Piping and Instrumentation Diagram (P&ID)
Emergent BioSolutionsNYSE: EBS: Develops and manufactures vaccines and therapeutics for health threats.
3+ YOEBachelor's or master's degree in applied science, 3–5 years preferred, GMP raw-material assay experience preferred, and proficiency in laboratory methods, LIMS, quality systems, cGMP, CFR, USP, and Microsoft Office tools.
LIMS, FTIR, UV Vis Spectrophotometry, Gel Electrophoresis, HPLC, Microsoft Office, Microsoft Excel, Microsoft Project, 5S, Kaizen, GMP, cGMP, CFR, USP, IOPQ, CAPA
Shawmut Design and Construction: National construction management firm specializing in complex building projects.
10+ YOERequires 10+ years construction experience, 5+ years on multiple cGMP projects, experience across full cGMP lifecycle, leadership and pursuit experience, and proficiency scheduling with Microsoft Project or P6.
Senior Manager Quality, EM&S Gen Med North America
Framingham, Massachusetts, United States
$90k-$130k/yrHybridFull Time
SanofiEuronext Paris: SAN: Researches, develops, and manufactures medicines and vaccines globally.
3+ YOEBachelor's in a science field, 3+ years in pharmaceutical or quality operations with cGMP experience, strong cGMP/QMS knowledge, audit and CAPA experience, project management, and willingness to travel 25–30%.
Genezen: Produces viral vectors for cell and gene therapy programs.
2+ YOEHigh school diploma, 2+ years of cGMP shipping/receiving experience, 1 year of cGMP experience, forklift experience, Excel skills, English fluency, and ability to lift 40 pounds.
Anika TherapeuticsNASDAQ: ANIK: Develops and manufactures products for early intervention orthopedic care.
4+ YOEHigh school diploma or equivalent; 4+ years cGMP-regulated manufacturing QA/QC experience; experience with material inspection, documentation review, ERP, Microsoft Word/Excel/Outlook; knowledge of cGMP and Good Documentation Practices.
Microsoft Word, Microsoft Excel, Microsoft Outlook, ERP
Rentschler Biopharma: Provides biopharmaceutical contract development and manufacturing services.
3+ YOEcGMP analytical data review experience in QC labs; B.S. in chemistry/biology/chemical engineering or related; 3+ years cGMP analytical lab experience; knowledge of HPLC, LIMS, data integrity, and strong communication skills.
HPLC, PA800, CS2500, SDS Page, LIMS, EMPOWER, Microsoft Outlook, Microsoft Word, Microsoft Excel, Microsoft PowerPoint