Job Description
Responsibilities
- Support day-to-day Quality Assurance (QA) operations for biologics manufacturing activities.
- Review and approve batch manufacturing records, logbooks, and GMP documentation for accuracy and compliance.
- Assist with deviation investigations, CAPA tracking, and quality event management.
- Support product disposition activities and ensure timely release documentation is completed.
- Participate in internal audits, regulatory inspections, and quality compliance initiatives.
- Collaborate with Manufacturing, QC, Engineering, and Supply Chain teams to maintain GMP standards and resolve quality issues.
- Degree in Life Sciences, Biotechnology, Pharmacy, Chemistry, or a related field.
- 2-3 years of experience in a Biopharmaceutical plant with Quality Operations QA experience.