BioTalent
Senior Quality Engineer - Electronics
BioTalent, San Francisco, California, United States, 94199
Overview
We’re seeking a Senior Quality Engineer to support product design, development, and manufacturing of electronic and electromechanical medical devices. This role ensures compliance with QMS, ISO, and FDA regulations while driving quality across development and commercial operations. Base pay range $135,000.00/yr - $165,000.00/yr Location:
SF Bay Area - East Bay Compensation:
$135,000 – $165,000 Type:
On-site Key Responsibilities
Lead quality efforts on cross-functional project teams for new and existing products Support design control, risk management, and product verification/validation Develop and validate test methods, inspection procedures, and quality standards Analyze non-conformances, lead investigations, and support CAPA/NCR boards Prepare documentation and support audits (FDA, FDB, notified body) Provide training, guidance, and mentorship to team members Collaborate with contract manufacturers on electromechanical devices and PCBAs Qualifications
Bachelor’s degree in Engineering, Life Science, or related field (advanced degree preferred) 5+ years of quality assurance experience in medical devices or regulated industry Hands-on experience with PFMEA, NCRs, CAPAs, change control, and failure investigations Familiarity with electronics/PCBA manufacturing and contract manufacturing Background in auditing, sterilization, design reviews, and/or project management Working Conditions
Mix of office, lab, and cleanroom environments Limited travel (0–10%) Ability to lift up to 25 lbs and support inspections, audits, and hands-on testing
#J-18808-Ljbffr
We’re seeking a Senior Quality Engineer to support product design, development, and manufacturing of electronic and electromechanical medical devices. This role ensures compliance with QMS, ISO, and FDA regulations while driving quality across development and commercial operations. Base pay range $135,000.00/yr - $165,000.00/yr Location:
SF Bay Area - East Bay Compensation:
$135,000 – $165,000 Type:
On-site Key Responsibilities
Lead quality efforts on cross-functional project teams for new and existing products Support design control, risk management, and product verification/validation Develop and validate test methods, inspection procedures, and quality standards Analyze non-conformances, lead investigations, and support CAPA/NCR boards Prepare documentation and support audits (FDA, FDB, notified body) Provide training, guidance, and mentorship to team members Collaborate with contract manufacturers on electromechanical devices and PCBAs Qualifications
Bachelor’s degree in Engineering, Life Science, or related field (advanced degree preferred) 5+ years of quality assurance experience in medical devices or regulated industry Hands-on experience with PFMEA, NCRs, CAPAs, change control, and failure investigations Familiarity with electronics/PCBA manufacturing and contract manufacturing Background in auditing, sterilization, design reviews, and/or project management Working Conditions
Mix of office, lab, and cleanroom environments Limited travel (0–10%) Ability to lift up to 25 lbs and support inspections, audits, and hands-on testing
#J-18808-Ljbffr