Quality Systems Supervisor – GMP Compliance & KPIs

PCI Pharma Services; San Diego (CA); On-site; USD 76,000 - 95,000; Full time

Benefits offered by this job

paid time off

health insurance (dental & vision)

flexible spending account

401(k) plan

Job summary

PCI Pharma Services is seeking a Supervisor, Quality Systems at our San Diego site to oversee the Quality Management System for GMP operations. You will ensure inspection-ready records, drive QMS improvements, and coordinate documentation reviews and approvals.

The role requires 5-7+ years in QA/QMS, strong GMP knowledge, and collaborative leadership with Manufacturing, QC, Validation, and Engineering. On-site, 8:00 AM–5:00 PM.

Qualifications

• 5-7+ years of experience in Quality Assurance, Quality Systems, pharma manufacturing, biotech, or related regulated industry.
• Demonstrated knowledge of GMP regulations and quality-system requirements (FDA/EU/international).
• Experience coordinating deviations, investigations, CAPAs, change controls, document control, training, audits, inspections, and quality metrics.

Responsibilities

• Supervise daily execution of Quality Systems processes and activities.
• Ensure quality records are complete, accurate, timely, and inspection-ready.
• Coordinate review, approval, tracking, and closure of QMS records (deviations, investigations, CAPAs, change controls, events, document control, training).
• Provide coaching and performance feedback to QA Systems team members.
• Support implementation and continual improvement of site QMS procedures and programs.

Skills

Quality Systems leadership

GMP regulations

Regulatory inspections

Quality data reporting

Education

Bachelor's degree in Life Sciences

High School diploma or equivalent

Tools

Electronic Quality Management Systems

Job description

PCI Pharma Services is seeking a Supervisor, Quality Systems at our San Diego site to oversee the Quality Management System for GMP operations. You will ensure inspection-ready records, drive QMS improvements, and coordinate documentation reviews and approvals.

The role requires 5-7+ years in QA/QMS, strong GMP knowledge, and collaborative leadership with Manufacturing, QC, Validation, and Engineering. On-site, 8:00 AM–5:00 PM.