Parenteral Manufacturing Technician

About the role

We are seeking a dedicated Parenteral Manufacturing Technician to support our aseptic production lines. The role involves ensuring compliance with GMP standards and maintaining the qualification status of critical equipment.

Key responsibilities

• Sign and maintain Parenteral GMP documentation and equipment cleaning/sanitization logs.
• Perform equipment qualification and re‑qualification activities for Vial Filling, PFS Filling, Infusion Bag, and API aseptic lines.
• Oversee qualification and re‑qualification of aseptic and freeze‑drying areas within the manufacturing facility.
• Execute any additional tasks assigned by the supervisor to ensure smooth operation of the production environment.

Required profile

• Minimum 3 years of experience in pharmaceutical or parenteral manufacturing.
• ITI or Diploma level technical education.
• Authorized to sign GMP documents and cleaning logs.
• Strong understanding of equipment qualification processes.

Required skills

• GMP documentation handling
• Equipment qualification and re‑qualification
• Aseptic processing and area management
• Freeze‑drying operation qualification
• Cleaning and sanitization log maintenance