Quality Assurance Specialist

Peregrine Team

San Diego, California

JOB DETAILS
SKILLS
Biotech and Pharmaceutical, Change Control, Communication Skills, Corrective and Preventative Action (CAPA) Systems, Cross-Functional, Current Good Manufacturing Practice (cGMP), Detail Oriented, Documentation, External Audit, FDA (Food and Drug Administration), FDA Requirements, GMP (Good Manufacturing Practices), Internal Audit, Maintain Compliance, Manufacturing, Manufacturing Operations, Manufacturing Requirements, Quality Assurance, Quality Control, Quality Management, Regulatory Compliance, Root Cause Analysis, Standard Operating Procedures (SOP), Systems Maintenance
LOCATION
San Diego, California
POSTED
30+ days ago

Peregrine Team is hiring a Quality Assurance Specialist to support a growing biotech organization focused on developing and manufacturing innovative therapies. This role will play a key part in maintaining quality systems, supporting audits, and ensuring compliance with cGMP standards across manufacturing and operations.

Key Responsibilities

  • Review and approve batch records, deviations, and change controls in accordance with cGMP guidelines
  • Support internal and external audits, including FDA inspections
  • Maintain and update SOPs, quality documentation, and training records
  • Partner cross-functionally with manufacturing, regulatory, and quality control teams
  • Assist with CAPA investigations and root cause analysis

Qualifications

  • Bachelor’s degree in a scientific discipline or related field
  • 3–5+ years of experience in a GMP-regulated environment (biotech/pharma preferred)
  • Strong understanding of FDA regulations and quality systems
  • Detail-oriented with strong documentation and communication skills

About the Company

P

Peregrine Team