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.
- 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.
- 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.
Salarisomschrijving
€6200 - €6200 monthly