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
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
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.
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.
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.
Atlanta or Toronto or Detroit or Boston or Bangor or New York City or Schenectady
$94k-$156k/yrRemoteFull Time
GE VernovaNYSE: GEV: Designs and services technologies for global power generation and electrification.
Bachelor's in engineering or related, proven quality experience in manufacturing/field service, expertise in nonconformance, RCA/CAPA and continuous improvement, willingness to travel ~10–30%.
TE ConnectivityNYSE: TEL: Manufacturer of electronic connectors and sensors for global industries.
5+ YOEBachelor's in engineering/science or related, 5+ years related experience, ISO 13485 knowledge, audit and CAPA experience, eQMS experience, strong investigation and communication skills.
LI-COR: Develops scientific instruments for biotechnology and environmental research
3+ YOEBachelor's in engineering, 3+ years quality engineering in manufacturing, experience with ISO 9001, root cause analysis, CAPA, GD&T, and strong analytical and communication skills.
RepligenNASDAQ: RGEN: Develops and manufactures bioprocessing technologies for pharmaceutical drug production.
Experience with batch record review, GDP/ISO9001, deviations/CAPA/change control, Electronic and paper batch records, SAP and Microsoft Office. Bachelor’s preferred or equivalent experience.
Microsoft Word, Microsoft PowerPoint, Microsoft Excel, Microsoft Outlook, SAP, Electronic Batch Records, Paper Batch Records
Sheffield Pharmaceuticals: Manufacturer of over-the-counter pharmaceuticals and personal care products.
Maintain QA documentation, review batch records, coordinate CAPAs and audits. Requires attention to detail, knowledge of cGMP and good documentation practices, and proficiency with Word, Excel, and PowerPoint.
Microsoft Word, Microsoft Excel, Microsoft PowerPoint
Supplier Quality Engineer III - External Operations ENDO
Marlborough, Massachusetts, United States
$82k-$156k/yrHybridFull Time
Boston ScientificNYSE: BSX: Manufacturer of interventional medical devices and technologies.
3+ YOEBS in engineering with 3+ years relevant experience; supplier quality, audits, CAPA/SCAR, process validation, design controls, project management, and ability to travel up to 25%.