Parenteral Manufacturing Technician

About the role

The Parenteral Manufacturing Technician plays a critical role in ensuring the quality and compliance of aseptic pharmaceutical production. Working within a regulated environment, the technician supports equipment qualification, line operations, and documentation for GMP compliance.

Key responsibilities

• Sign off Parenteral GMP documents and cleaning/sanitisation logs as an authorized doer.
• Participate in equipment qualification and re‑qualification activities.
• Oversee the Vial Filling Line, PFS Filling Line, Infusion Bag Line, and API aseptic area.
• Manage qualification and re‑qualification of aseptic and freeze‑drying areas.
• Execute any additional tasks assigned by the supervisor.

Required profile

• Minimum 3 years of experience in pharmaceutical or parenteral manufacturing.
• Technical qualification such as ITI or a relevant diploma.
• Authorized to sign GMP documentation and cleaning logs.
• Demonstrated ability to work in a regulated, aseptic environment.

Required skills

• GMP documentation and compliance.
• Equipment qualification and re‑qualification procedures.
• Aseptic processing knowledge.
• Freeze‑drying operations.