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Principal Supplier Quality Engineer

Job in Fremont, Alameda County, California, 94537, USA
Listing for: BioTalent Ltd
Part Time position
Listed on 2026-08-29
Job specializations:
  • Quality Assurance - QA/QC
    Quality Engineering, Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 150000 - 210000 USD Yearly USD 150000.00 210000.00 YEAR
Job Description & How to Apply Below

Principal Supplier Quality Engineer | Fremont, CA (Onsite 3x/week with up to 50% travel to South Bay)

We're looking for a Principal Supplier Quality Engineer to build our supplier quality management program from the ground up. This is a brand-new role — you'll be the dedicated supplier quality authority, owning the full lifecycle of supplier qualification, auditing, monitoring, and performance management for a fast-growing medical device company.

You'llwear multiple hats, partner cross-functionally, and have real influence in shaping how we manage suppliers as we scale.

What You'll Do
  • Design, implement, and continuously improve our Supplier Quality Management Program — supplier qualification, controls, auditing, monitoring, and risk management
  • Lead qualification and oversight of contract manufacturers, sterilization providers, and critical suppliers
  • Plan, conduct, and report on supplier audits and assessments
  • Own SCAR management from initiation through effectiveness verification
  • Investigate supplier quality issues, drive root cause analysis and corrective action
  • Build and maintain supplier scorecards, risk profiles, and performance metrics
  • Partner cross-functionally with Engineering, Operations, Manufacturing, Supply Chain, and Regulatory Affairs
  • Support FDA inspections, notified body audits, and customer audits
  • Apply risk-based decision-making per ISO 14971
What You Bring
  • 8-10+ years of Quality Assurance / Supplier Quality experience in the medical device industry
  • Strong working knowledge of FDA 21 CFR Part 820/QMSR, ISO 13485, and ISO 14971
  • Proven experience qualifying, auditing, and managing suppliers, including SCAR management
  • Background in medical robotics, orthopedic implants, capital equipment, or electromechanical devices strongly preferred but not required
  • Experience building a supplier quality program from scratch a big plus
  • ASQ CQE, CSQP, CQA, or ISO 13485 Lead Auditor certification preferred
  • Comfortable with up to 50% travel to our primary supplier located in South Bay
Logistics
  • Onsite 3 days/week when not traveling to South Bay Supplier
  • Full medical, dental, and vision; KPI-based bonus; stock options
  • Please note:

    this role is not eligible for visa sponsorship, including TN visas
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