Thermo Fisher ScientificNYSE: TMO: Sells equipment and chemicals for scientific research and healthcare.
2+ YOE2+ years quality or manufacturing experience in a regulated industry; BS preferred; perform RCA, implement CAPAs, statistical analysis, knowledge of ISO 13485/21 CFR 820; strong communication and Microsoft Office skills.
Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Minitab, JMP, TrackWise CAPA Management System
Senior Quality Systems Engineer- CAPA/Complaints Support - Medical Device #8161
Boston, Massachusetts, United States
OnsiteContract, Full Time
ECI: Provides regulatory and engineering consulting for life sciences companies.
5+ YOE5+ years medical device experience, Bachelor’s in biomedical/mechanical/electrical engineering required, experience executing CAPA, regulatory knowledge for Class II/III devices, strong analytical and problem-solving skills.
5+ YOEQuality engineer with data analytics experience; supplier, manufacturing, and design quality focus; CAPA and PPAP familiarity; cross-functional collaboration.
Loos & Co: Manufactures mission-critical wire, rope, and cable assemblies.
10+ YOE10+ years quality experience in AS9100 manufacturing, supervisory experience, inspection and measurement skills, root cause analysis, CAPA, strong communication, and Microsoft Office proficiency.
AstroNovaNASDAQ: ALOT: Designs and produces industrial printers and aerospace electronics.
7+ YOEBachelor’s in Engineering, Quality, Manufacturing or related field; 7+ years in a regulated manufacturing environment; AS9100/ISO 9001 knowledge; audits and CAPA experience; leadership ability.
AS9100, ISO 9001, FAA, DAR, CAPA, QMS, Audit management
Merck KGaA, Darmstadt, GermanyXETRA: MRK: Science and technology specializing in healthcare, life science, and electronics.
1+ YOEBachelor's in engineering or science,1+ year quality engineering in a regulated manufacturing environment; knowledge of cGMP/ISO/FDA, investigations, CAPA, FMEA, validation, and statistical analysis (Minitab).
MerckXETRA: MRK: A science and technology providing healthcare, life science, and electronics solutions.
1+ YOEBachelor's in engineering or science, 1+ years quality engineering experience in regulated manufacturing; knowledge of cGMP/ISO/QMS, investigations, FMEA, CAPA, data analysis (Minitab), and documentation control.
Quantic Evans: Manufactures high-energy density capacitors for aerospace and defense.
Experience in quality or manufacturing roles, familiarity with ISO 9001/AS9100, NC/CAPA processes, document control, audit support, Excel/ERP proficiency, strong written/verbal communication and attention to detail.
Microsoft Excel, Microsoft Office, ERP, FMEA, CAPA, IPC standards
MedtronicNYSE: MDT: Developing and manufacturing medical technologies and therapies globally.
2+ YOEBachelor's degree plus 2 years relevant experience (or advanced degree), experience in regulated manufacturing, knowledge of design control, validation, CAPA, FMEA, Six Sigma, DOE, strong analytical and communication skills.
Associate Director, Clinical Quality and Continuous Improvement
Cambridge or United States
$165k-$223k/yrRemoteFull Time
Alnylam PharmaceuticalsNASDAQ: ALNY: Develops RNAi therapeutics to treat rare and common diseases.
8+ YOEBachelor's in life sciences required; 8+ years in GCP Quality Assurance/Clinical Quality; experience with process improvement (DMAIC/Lean), RCA, CAPA, inspection readiness, quality metrics, and cross-functional influence.
Johnson & JohnsonNYSE: JNJ: Develops and manufactures pharmaceutical drugs and medical devices.
4+ YOEBachelor's in engineering, minimum 4 years manufacturing engineering in a regulated industry, experience with yield improvement, CAPA, IQ/OQ/PQ, Lean/Six Sigma, product introductions, and strong problem-solving skills.
CAPA, IQ/OQ/PQ, Robotic Automation, Good Manufacturing Practices (GMP), Lean Manufacturing, Six Sigma
AbbottNYSE: ABT: Provides medical devices, diagnostics, and science-based nutritional products.
3+ MgmtBachelor's in biomedical engineering, nursing or related (or equivalent experience). 3+ years managing a team. Knowledge of domestic/international medical device regulations, risk assessment, CAPA and audit management, and advanced analytical and PC skills.
Engineer Process Development Environmental & Contamination Control
West Greenwich, Rhode Island, United States
$88k-$119k/yrOnsiteFull Time
AmgenNASDAQ: AMGN: Develops and manufactures biotechnology medicines for serious diseases.
2+ YOEEducation plus engineering/operations experience (options: HS+8yrs, Associate+6yrs, Bachelor+2yrs, or Master). Prefer 2+ years pharma/biopharma cGMP experience, strong communication, and experience with EBR/DeltaV/CAPA.
Envision Energy: Manufacturer of smart wind turbines and energy storage solutions.
3+ YOEBachelor's in materials or mechanical engineering,3–7 years quality engineering in manufacturing, practical command of FMEA, SPC, MSA/Gage R&R, 8D/CAPA, ISO 9001 QMS experience, strong communication skills.
FMEA, SPC, DOE, MSA/Gage R&R, 8D, CAPA, APQP, PPAP, Design of Experiments (DOE), Six Sigma, ISO 9001, ISO 22734, IEC 62282, NFPA 2
HologicNASDAQ: HOLX: Develops medical technology for women's healthcare and diagnostics.
7+ YOEBachelor's degree or equivalent,7+ years medical device quality experience,knowledge of ISO 13485,ISO 14971,FDA and EU MDR/IVDR,cAPA,CAPA,PFMEA,validation and risk management;ASQ CQE or Six Sigma preferred.
ISO 13485, ISO 14971, EU MDR, IVDR, cGMP, Six Sigma, SPC, DOE
Associate Director, Quality Systems - Cell and Gene Therapies (VCGT)
Boston, Massachusetts, United States
$148k-$222k/yrHybridFull Time
Vertex PharmaceuticalsNASDAQ: VRTX: Develops and sells prescription drugs for serious genetic diseases.
10+ YOEBachelor's degree and 10+ years experience in quality systems/GxP with expertise in risk management, data integrity, audits, CAPA, investigations, and project leadership.
VulcanForms: Provides industrial-scale metal additive manufacturing and precision machining services.
3+ YOE3+ years in medical device manufacturing with Final Release/Document Control; read blueprints; review DHRs/Batch Records; manage nonconformances and CAPAs.