Pharmaceutical Manufacturing Technician (Parenteral)

About the role

The company is seeking a skilled Technician to support its parenteral manufacturing operations. The role involves handling GMP documentation, equipment qualification, and ensuring aseptic and freeze‑drying areas meet regulatory standards.

Key responsibilities

• Prepare, sign and maintain Parenteral GMP documents.
• Maintain equipment and area cleaning/sanitization logs.
• Execute equipment qualification and re‑qualification activities.
• Oversee Vial Filling Line, PFS Filling Line, Infusion Bag Line, and API aseptic area operations.
• Manage qualification and re‑qualification tasks for aseptic and freeze‑drying areas.
• Perform any additional tasks assigned by the supervisor.

Required profile

• Minimum 3 years of experience in pharmaceutical or related manufacturing.
• ITI or Diploma qualification in a relevant technical field.
• Ability to work independently and sign off on GMP documents.

Required skills

• GMP documentation handling.
• Equipment qualification and re‑qualification.
• Aseptic processing knowledge.
• Freeze‑drying area operations.