Responsibilities:
- Review executed component records and release media / buffer / raw material in SAP.
- Verify analytical data and confirm quality control results meet specifications.
- Ensure compliance with SOPs, cGMP, GDP, and regulatory requirements.
- Identify and report deviations, errors, and variances to Quality Assurance.
- Support audits and inspections by preparing and organizing batch documentation.
- Any other duties as assigned.
About You:
- Bachelor’s degree in a scientific discipline (e.g., pharmacy, chemistry, life sciences)
- Preferably with 1–2 years of experience in Good Manufacturing Practice (GMP) and Good Documentation Practice (GDP), and in Biologics manufacturing.
- Strong attention to detail and analytical skills
- Proficiency in SAP systems.
- Excellent communication and organizational abilities.
Contract Period: 16 months