Are you looking to develop your skills as a production operator in a GMP-regulated pharmaceutical environment? As an Operator B FPL, you contribute to the first stage of the production process, where plasma is prepared for further processing into life-saving plasma-derived medicines. You carry out assigned production activities according to established procedures, perform quality checks, and help maintain a safe, clean, and efficient production environment.
What will you do?
As Operator B FPL, you will:
- Perform assigned production activities according to SOPs, GMP requirements, and production planning.
- Prepare and process plasma and intermediate products according to established procedures and within the scope of your training.
- Carry out routine production calculations, including dilutions, and check the results according to prescribed instructions.
- Prepare equipment, materials, and workstations for production.
- Complete batch records, logbooks, and other GMP documentation accurately and on time.
- Register raw materials, consumables, and production data in the relevant information systems.
- Perform routine quality checks, sampling, and inspections of products, processes, and materials, and record the results.
- Identify, document, and promptly report deviations or unexpected results to the Senior Operator or Supervisor.
- Support routine validation, calibration, and self-inspection activities according to procedures and within the scope of your training.
- Clean equipment, materials, and work areas in accordance with GMP and hygiene standards.
- Perform minor equipment maintenance and resolve simple malfunctions within your training and approved procedures, escalating technical issues when needed.
- Monitor material supplies and help ensure timely replenishment to support daily production.
What do you bring?
- An MBO-level qualification in a relevant technical, laboratory, or pharmaceutical field, or an equivalent level gained through experience.
- Experience in a similar function within a GMP controlled environment.
- Basic knowledge of GMP, SOPs, batch documentation, and quality procedures, or a willingness to develop this knowledge through training.
- An aptitude for working with production equipment and automated systems.
- The ability to follow procedures accurately, perform routine calculations, and recognize and report deviations.
- An accurate, quality-conscious approach and the ability to work effectively as part of a team.
- Good command of Dutch, both written and spoken, as documentation within the department is available only in Dutch.
- Willingness to work morning, evening, and night shifts in a semi-continuous schedule.
What do we offer?
- A 40-hour workweek in a semi-continuous schedule, including morning, evening, and night shifts.
- Job Scale 4, with a gross monthly salary between €2,989.14 and €4,296.95, depending on your experience.
- A 25.30% shift allowance.
- An 8.33% end-of-year bonus and 8.33% holiday allowance.
- A €2,100 personal development budget every three years.
- Travel allowance from the first kilometer.· Travel allowance of €0.25 per kilometer for commuting by car, up to 30 km each way, or reimbursement for eligible public transport.
- Pension through Pensioenfonds Zorg & Welzijn (PFZW).
- A GMP production environment where you can develop your skills and contribute to the production of life-saving plasma-derived medicines.
Solicitation is not appreciated. Prothya does not accept unsolicited assistance from agencies for this vacancy. CVs submitted (in any form) by recruitment agencies to any Prothya employee without a valid written search assignment shall be considered the property of Prothya, for which no compensation is due in any way.