Quality Assurance Consultant

Tasks

• Review and address manufacturing deviations, CAPAs, and quality findings identified during internal facility and manufacturing line audits.
• Support root cause investigations and develop effective corrective and preventive action plans.
• Drive timely resolution of outstanding quality issues and support remediation activities.
• Evaluate manufacturing processes and documentation to identify compliance gaps and improvement opportunities.
• Review GMP batch production records for completeness, accuracy, procedural adherence, and regulatory compliance.

Requirements

• Experience in Quality Assurance, Quality Compliance, or Manufacturing Quality within the pharmaceutical or biopharmaceutical industry.
• Hands-on experience investigating manufacturing deviations and managing CAPAs in a GMP-regulated environment.
• Experience reviewing GMP batch records and manufacturing documentation.
• Strong knowledge of GMP compliance, quality documentation, and investigation processes.

How to apply

• Connect with us or send your resume by email.
• Apply through the link.

Location

• San Jose, CA