Quality Operations Specialist (Pharma/Biotech)

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. Duration: 6 months