For our partner located in the canton of Neuchâtel, GI Life Sciences is looking for a:

Bulk Technician

Temporary position

Start: ASAP

Your mission:

Your mission will be to ensure the manufacturing activities of products (tablets), in compliance with GMP / cGMP regulations, hygiene rules, and safety. You must comply with the procedures defined by the pharmaceutical site quality system.

Your tasks:

• Carry out production operations such as weighing materials, preparing powder blends, and operating automated lines.
• Provide technical support to operators in production activities.
• Master the ERP tool (MES) in managing batch records and associated consumptions.
• Master and perform cleaning of equipment, materials, and rooms related to the different production stages.
• Perform format changes and production line clearance.
• Update and create technical documents necessary for the operation of equipment and the line (instructions for use, cleaning).
• Control, record, and complete pre-established work documents to ensure tracking of operations performed (batch records completed according to GMP).
• Carry out basic physical checks of manufactured products.
• Participate in and support the validation of industrial processes and the manufacture of validation batches.
• Generate maintenance intervention requests in case of equipment failure and ensure follow-up until production resumes.
• Analyse equipment failures and support maintenance during interventions.
• Open deviations in the quality IT system.
• Perform format changes and basic adjustments defined in procedures.
• Train new employees and operators on the different production lines and be the training reference.
• Report hazardous situations, near misses/incidents, and accidents that may occur on site to your direct supervisor and the EHS department.

Your profile:

• Have a CFC-level qualification and 5 years’ experience in pharmaceutical production or ideally 3 years as a technician in the pharmaceutical industry.
• Have perfect command of French and English (minimum B1).
• Have thorough knowledge of the GMP environment and good knowledge of the pharmaceutical industry, particularly in the powder blending and compression sector.