Supplier Quality Engineer (Pharmaceutical)
Wilson, North Carolina
Job Id:
0000177771
Job Category:
Life Sciences
Job Location:
Wilson, North Carolina
Security Clearance:
No Clearance
Business Unit:
Piper Companies
Division:
Not Defined
Position Owner:
Jake Maehrer
Piper Companies is seeking a Supplier Quality Engineer to support supplier onboarding and quality activities for an industry-leading pharmaceutical company in Wilson, NC.
Responsibilities of the Supplier Quality Engineer
- Support supplier qualification, onboarding, and compliance activities.
- Manage supplier documentation, quality deliverables, and outstanding actions.
- Coordinate supplier audits and ongoing quality oversight.
- Collaborate with Procurement, Quality, Engineering, and cross-functional teams.
- Track supplier activities and ensure timely completion of deliverables.
Qualifications of the Supplier Quality Engineer
- 3–5 years of experience in Supplier Quality, Supplier Management, Quality Systems, or related fields.
- Experience with supplier onboarding, documentation, and compliance.
- Pharmaceutical or life sciences experience preferred.
- Strong organizational, communication, and problem-solving skills.
- Bachelor’s degree preferred
Compensation & Benefits:
- Compensation: $35-45/hr.
- Long Term Contract
- Hybrid Schedule
- Comprehensive Benefits: Medical, Dental, Vision, 401(k), Sick Leave (as required by law), and Paid Holidays
Application Period: This position opens for applications on 11/2/2026 and will remain open for a minimum of 30 days from the posting date.
Keywords: Supplier Quality, Supplier Quality Assurance (SQA), Supplier Quality Engineering (SQE), Supplier Management, Vendor Management, Supplier Qualification, Supplier Audits, Quality Management Systems (QMS), GMP, cGMP, GxP, FDA Regulations, ISO 13485, ISO 9001, CAPA, Root Cause Analysis, Deviation Management, Nonconformance Management, Change Control, Risk Management, Quality Agreements, Supplier Performance, Supplier Monitoring, Quality Investigations, Audit Readiness, Regulatory Compliance, Continuous Improvement, SCAR, 21 CFR Part 820, Pharmaceutical, Biotechnology, Medical Devices, Life Sciences.
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