Parenteral Manufacturing Technician

About the role

We are looking for a Technician with at least three years of experience in parenteral manufacturing. The role focuses on maintaining GMP compliance, overseeing equipment qualification, and supporting aseptic and freeze‑drying operations within a pharmaceutical production environment.

Key responsibilities

• Authorize and sign Parenteral GMP documents and equipment/area cleaning‑sanitization logs.
• Participate in equipment qualification and re‑qualification activities.
• Manage qualification and re‑qualification tasks for the Vial Filling Line, PFS Filling Line, Infusion Bag Line, and API aseptic area.
• Oversee aseptic area and Freeze‑Drying area qualification/re‑qualification in the parenteral manufacturing zone.
• Execute any additional tasks assigned by the supervisor.

Required profile

• Minimum 3 + years of relevant experience.
• ITI or Diploma qualification.
• Authorized to sign GMP documentation and cleaning logs.
• Ability to work in a regulated pharmaceutical environment.

Required skills

• GMP documentation and compliance.
• Equipment qualification and re‑qualification.
• Cleaning and sanitization log management.
• Aseptic processing of vial, PFS, and infusion bag lines.
• Freeze‑drying area qualification.