Greenfield Global: Produces high-purity alcohols, specialty solvents, and sustainable biofuels.
7+ YOEBachelor's degree, 7+ years in quality or supplier quality within a GMP/ISO regulated environment; working knowledge of ISO 9001, IPEC-PQG GMP, EXCiPACT; experience with supplier audits, supplier development, QMS, SCAR/CAPA, and risk-based supplier quality.
ISO 9001, IPEC-PQG GMP, EXCiPACT, QMS, SCAR, CAPA, Management of Change (MoC)
HyperfineNasdaq: HYPR: Develops and sells portable MRI brain imaging systems.
5+ YOELead supplier quality activities including supplier qualification, audits, NCs/CAPAs/SCARs, product release, risk management, and continuous improvement in a regulated medical device environment.
BDNYSE: BDX: Manufactures medical devices, surgical instruments, and pharmacy automation systems.
3+ YOEBachelor's degree, 3 years manufacturing experience, strong problem-solving and CI skills, experience with process validation, CAPA, change control, and manufacturing quality support for 24/7 operations.
Curtiss-WrightNYSE: CW: Engineers and manufactures critical components for aerospace and defense.
1+ YOEInspect materials and products, perform measurements and tests, document results, identify non-conformances, support CAPA, read blueprints, and use measuring instruments; 1-2 years inspection experience preferred.
SafarilandNYSE: CDRE: Manufacturer of tactical holsters and body armor for professionals.
5+ YOELead ISO 9001 compliance and QMS, manage audits, lead quality team, drive CAPA and continuous improvement (Lean/Six Sigma), supplier quality, inspection/testing, and use measuring/calibration tools.
Microsoft Word, Microsoft Excel, Microsoft Access, Microsoft PowerPoint
CooperSurgicalNasdaq: COO: Manufactures medical devices for fertility and women's health.
10+ YOELead supplier quality strategy and governance in regulated medical device environments; expertise in FDA QSR, ISO 13485, EU MDR, ISO 14971, audits, CAPA/SCAR, RCA/FMEA, and supplier development.
Microsoft Office, Minitab, ERP systems, eQMS platforms
MedtronicNew York Stock Exchange: MDT: Develops and manufactures medical devices and digital health solutions.
4+ YOEDegree in packaging/mechanical/manufacturing engineering, 4+ years experience (Bachelors) or equivalent, experience in regulated packaging operations, IQ/OQ/PQ validation, CAPA, Lean/Six Sigma, and project management skills.
MedtronicNew York Stock Exchange: MDT: Develops and manufactures medical devices and digital health solutions.
2+ YOEBachelor's in engineering/science + 4+ years (or advanced degree + 2+ years, or PhD) in engineering/quality. Experience in process validation, root cause/CAPA, statistical analysis (e.g., Minitab), and regulated manufacturing (FDA/CFR) preferred.
First Class Air Support: Distributes aftermarket aircraft components and provides aviation repair services.
7+ YOE3+ Mgmt7–10+ years in an FAA Part 145 repair station or aviation MRO, 3+ years leadership in quality/safety/inspection, knowledge of FAA/EASA regulations, ability to manage SMS, CAPA, audits, inspections, and airworthiness release processes.
FAA Form 8130-3, EASA Form 1, Safety Management System (SMS)
Development Scientist II, Analytical Development and Clinical QC (ADQC)
New Haven, Connecticut, United States
OnsiteFull Time
AstraZenecaLondon Stock Exchange: AZN: Global biopharmaceutical developing and manufacturing prescription medicines.
2+ YOEAdvanced MS or PhD in biochemistry/chemistry or related field, 2+ years (PhD) or 10+ years (MS) hands-on analytical development experience, cGMP/QC knowledge, LIR/CAPA investigation skills, MS Office proficiency, strong analytical and communication skills.
Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Veeva Vault (EQV), LIMS, ValGenesis, Kneat, JMP, Tableau, SAS, Microsoft SharePoint, BOX
CooperSurgicalNasdaq: COO: Manufactures medical devices for fertility and women's health.
7+ YOE7+ years quality engineering experience in medical devices; knowledge of FDA QMSR, ISO 13485, EU MDR, design controls, ISO 14971 risk management, FMEA/PPAP, change control and CAPA processes; bachelor’s degree required; ASQ CQE preferred.
Development Scientist II, Analytical Development and Clinical QC (ADQC)
New Haven, Connecticut, United States
OnsiteFull Time
Alexion Pharmaceuticals: Develops and manufactures treatments for rare and ultra-rare diseases.
2+ YOEResponsible for owning laboratory investigations (LIRs), closing OOS/OOT investigations, performing root cause analysis and CAPA, reviewing analytical data, ensuring cGMP compliance, and collaborating with QA/AD/stability; advanced degree in biochemistry/chemistry (MS or PhD) with relevant analytical development experience required.
Veeva Vault (EQV), LIMS, ValGenesis, Kneat, JMP, Tableau, SAS, Microsoft SharePoint, Microsoft Word, Microsoft Excel, Microsoft PowerPoint
CooperSurgicalNasdaq: COO: Manufactures medical devices for fertility and women's health.
10+ YOE10+ years quality engineering in medical devices (8+ with MS). Advanced knowledge of FDA QMSR (21 CFR 820), ISO 13485, EU MDR, design controls, ISO 14971, FMEA; experience with CAPA/change control, V&V, supplier engagement, and leading cross-functional teams.
Microsoft Excel, Microsoft Word, Microsoft PowerPoint, FMEA, PPAP
Manufacturing Manager Electrode Production (Torrington, CT, US, 06790)
Torrington, Connecticut, United States
OnsiteFull Time
FuelCell EnergyNASDAQ: FCEL: Produces fuel cell power plants and hydrogen generation systems.
7+ YOE3+ MgmtB.S. in engineering required, 7+ years manufacturing/process experience with 3+ years supervisory experience; lean manufacturing proficiency, experience in chemical/ceramic/powder or electrode manufacturing, and ability to lead 24/7 production teams.
Vantedge Medical: Manufacturer of precision metal components for medical device OEMs.
10+ YOE10+ years in manufacturing/process development/R&D engineering, experience with PECM/ECF and GD&T, strong project management, problem solving, and documentation skills; bachelor’s degree in engineering required.
908 DevicesNASDAQ: MASS: Handheld mass spectrometry devices for on-site chemical analysis.
5+ YOEBachelor's in engineering (Masters preferred), 5+ years quality engineering in electromechanical manufacturing, experience leading root cause analysis and corrective actions, familiarity with ISO 9001 and IPC-A-610, structured problem-solving (8D, FMEA, SPC), <10% travel.