Quality Operations Specialist (Pharma/Biotech) - Part-Time

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