Vacatures van Regiowerk Uitzendbureau in t Harde

Only candidates with a valid work permit will be considered. The client does not offer sponsorships.

Our client is looking for a Qualified Person who will play a key role in ensuring that our client's medicines meet the highest standards throughout the clinical development, supply chain, and product lifecycle. You will work cross-functionally with the production, distribution and supply chain department.

What your responsibilities will be:

• Certify batches of medicinal products and investigational medicinal products according to EU and international regulations
• Partner with internal teams to maintain compliance with quality policies, standards, and procedures.
• Serve as the QA contact for Deviations and CAPAs, ensuring proper investigation and resolution.
• Write, review, and approve procedures and job aids in line with regulatory and corporate requirements.
• Review and sign QP declarations and regulatory documentation supporting product filings.

Requirements

• Master degree in Pharmacy, Life Sciences (e.g. Medicine, Veterinary Medicine, Chemistry, Biology, etc.) or equivalent.
• Practical experience in a pharmaceutical GMP environment is a must.
• Minimum of 1 year work experience with a 5-year university degree.
• Minimum of 2 years of experience with a 4-year university degree.
• Excellent written and verbal communication skills in English.

Benefits

• A challenging work environment with excellent career development programs.
• Hybrid position, but at least 3 times a week on site in Breda.
• A competitive salary package.
• Reimbursement of travel expenses is dependable on travel distance.
• The contract will be through Undutchables.

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