11 quality assurance engineer jobs at 5 companies in River Bend, NC
1mo
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MCPP: Manager, Quality Assurance
Jacksonville or Kings Bay or Houston or Camp Lejeune or Norfolk
OnsiteFull Time
8+ YOE6+ MgmtU.S. citizen able to obtain Secret clearance; BA/BS in science/engineering or equivalent; 8+ years QA experience with 6 years management and 4 years supervisory experience; CMQ/OE within 1 year; Lean/Six Sigma experience.
ISO 9001:2015, Six Sigma, Lean
1mo
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Quality Engineer
Kinston, North Carolina, United States
OnsiteFull Time
3+ YOEABET-accredited engineering degree, 3-5 years aerospace/quality experience, RCCA and root cause analysis proficiency, technical writing and communication skills.
3w
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Quality Manager
Vanceboro, North Carolina, United States
$101k-$135k/yr OnsiteFull Time
5+ YOEBS in engineering, 5+ years QA (or 7-10 years mill/process engineering), ISO/internal audit experience, root-cause and corrective action expertise, SQC knowledge, Microsoft Office, Omega and Proficy familiarity.
Microsoft Office, Omega, Proficy
3mo
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Supervisor, Quality Control (2nd Shift) (Kinston, NC, US, 28504)
Kinston, North Carolina, United States
OnsiteFull Time
5+ YOEFive+ years QA/QC experience in FDA-regulated environment; associate or technical/engineering degree required or bachelor’s preferred; proficient with QC inspection, root cause analysis, and documentation; leadership experience of 10-15 people preferred.
Microsoft Word, Microsoft Excel, Master-control, SAP
1w
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Engineer/Scientist II, QC (Metrology)
Greenville, North Carolina, United States
OnsiteFull Time
2+ YOEBachelor's degree in applied science or equivalent, 2+ years calibrating and maintaining pharmaceutical laboratory instruments, GMP and quality systems knowledge, Microsoft Office proficiency, and English communication skills.
High-Performance Liquid Chromatography (HPLC), Gas Chromatography (GC), Fourier-Transform Infrared Spectroscopy (FTIR), Microsoft Office, Microsoft Word, Microsoft Excel, Microsoft PowerPoint
1mo
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Staff QA Engineer
Greenville, North Carolina, United States
OnsiteFull Time
6+ YOEIn-depth GMP and ISO 9001/13485 knowledge, audit and inspection experience, expertise in CAPA/change control/document control, FMEA and root cause analysis, validation (IQ/OQ/PQ), TrackWise/SAP experience, advanced degree +6 yrs or BS +8 yrs in technical field; travel up to 25%.
TrackWise, SAP, FMEA
2mo
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Staff Validation Engineer, Process and Cleaning
Greenville, North Carolina, United States
OnsiteFull Time
8+ YOE8+ years in process and/or cleaning validation in sterile/aseptic manufacturing; strong cGMP knowledge; data analysis; technical writing; cross-functional collaboration.
2w
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Product Compliant Investigator II - Medical Device
Greenville, North Carolina, United States
OnsiteFull Time
2+ YOEBachelor's in life/health science or engineering,2+ years pharma/biotech experience,knowledge of cGMP and quality systems,strong communication and organizational skills.
2mo
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Configuration Verification
Kinston, North Carolina, United States
OnsiteFull Time
1+ YOEConduct audits and BOM analysis to verify configuration control and compliance; manage configuration data and shipping documentation; coordinate with engineering, production, quality and customers; proficiency with Excel/PowerPoint; SAP/MES experience preferred; up to 5% travel.
Microsoft Excel, Microsoft PowerPoint, SAP, MES, Minitab, JMP
2mo
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Validation Manager
Greenville, North Carolina, United States
OnsiteFull Time
6+ YOE3+ MgmtBachelor's degree in engineering, science, chemistry, biology or related technical discipline; 6-8 years pharma/biotech manufacturing; 2+ years validation experience; 3+ years people management; strong cGMP knowledge; regulatory inspection experience.
cgmp, validation management, change control, statistical analysis, documentation tools
1mo
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QA Supervisor (1 Day Shift & 2 Night Shift Positions)
Greenville, North Carolina, United States
OnsiteFull Time
3+ YOE2+ MgmtBS degree required (biology/chemistry/engineering preferred), advanced degree preferred. 2–5 years QA experience in regulated manufacturing (3+ years typical), 2+ years supervisory experience, cGMP/ISO knowledge, batch record/CAPA experience, TrackWise and SAP proficiency.
TrackWise, SAP