Biopharma Formulation Technician II — cGMP Expert

Make it in the North; Groningen; Hybrid; EUR 42,000 - 56,000; Full time

Job summary

Thermo Fisher Groningen site is seeking a Formulation Technician II to join the OPS department. You will execute unit operations and measurements in a clean room under cGMP conditions, contribute to production under GMP standards, and maintain compliant documentation.

You will train coworkers, review and write documentation, support new procedures and equipment, and assist in validation protocols. The role requires attention to quality and timely corrective actions in a fast-paced

Responsibilities

• Executes several unit operations, manual operations and measurements in a clean room environment under cGMP conditions.
• Contributes to the departmental responsibility for production under GMP conditions of biopharmaceutical products and intermediates, including maintaining the production suites in proper condition (e.g. 5S, Fit & Finish inspections).
• Ensures GMP documentation is properly filled in during production as required by cGMP.
• Adds and implements corrective or preventive actions on execution level; trains co-workers unfamiliar with unit operations or equipment.
• Assists in execution of validation protocols for which a Technician II DSP technical skill is required.
• Trains co-workers that are unfamiliar with certain unit operation or handling of specific equipment, including approval of on-the-job trainings.

Job description

Thermo Fisher Groningen site is seeking a Formulation Technician II to join the OPS department. You will execute unit operations and measurements in a clean room under cGMP conditions, contribute to production under GMP standards, and maintain compliant documentation.

You will train coworkers, review and write documentation, support new procedures and equipment, and assist in validation protocols. The role requires attention to quality and timely corrective actions in a fast-paced