Technician I – Parenteral Manufacturing

About the role

The Technician I will support the Parenteral Manufacturing area by ensuring compliance with GMP standards, maintaining equipment cleanliness, and contributing to qualification activities. This position works on critical production lines such as vial filling, pre‑filled syringes, infusion bags, and freeze‑drying operations.

Key responsibilities

• Authorize and sign Parenteral GMP documents and equipment/area cleaning logs.
• Participate in equipment qualification and re‑qualification projects.
• Maintain and monitor the Vial Filling Line, PFS Filling Line, Infusion Bag Line, and API aseptic area.
• Execute qualification and re‑qualification tasks in aseptic and freeze‑drying areas.
• Perform any additional duties assigned by the supervisor.

Required profile

• Experience in a regulated pharmaceutical manufacturing environment.
• Understanding of GMP documentation and clean‑room procedures.
• Ability to work accurately with detailed logs and qualification records.
• Strong attention to detail and commitment to product safety.

Required skills

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

What we offer

• Opportunity to work on state‑of‑the‑art parenteral production lines.
• Professional development in pharmaceutical manufacturing.
• Collaborative team environment focused on quality and safety.