As a Production Engineer supporting our clinical supply production department for batch record review and continuous improvement projects: identifying improvements on quality, safety, efficiency.
Opportunity to get to know production departments hands on in the production environment.
The service involves getting to know the production department in shifts, review of the batch related documentation to allow for timely release of clinical batches to clinical supply.
After a while be the responsible person for continuous improvement projects: identifying improvements on quality, safety, efficiency and be a back-up for the shift production engineer when needed: the first point of contact for any production related issue such as assisting and coordinating activities related to technical breakdowns, carrying out and documenting root cause investigations in the event of quality deviations, and implementing minor and major changes to existing equipment within set deadlines.
Qualifications:
* Master's degree in relevant fields such as industrial, civil, or bio-engineering, or an (industrial) pharmacist degree, or equivalent experience
* Relevant service resources must possess perfect command of both Dutch and English
* Key competencies include strong analytical skills and problem-solving abilities, strong communication and interpersonal skills, and a structured, accurate, and independently organized approach to work
* Experience in a GMP environment is a benefit, along with a strong technical writing ability and interest in technology
* This position also require flexibility for shift work (early, late)