Key Responsibilities
- Perform QA review and approval of SAP Master Data activities, including critical value verification and Bills of Materials
- Review and approve artwork for medicinal products in line with regulatory and quality requirements
- Ensure QA systems are maintained, monitored, and continuously improved
- Author, review, and approve operational SOPs and Work Instructions
- Participate in QA-related projects and support quality investigations as required
- Identify, assess, and resolve data integrity issues, escalating where necessary
- Working Style & Collaboration
- Work under general direction, managing priorities within agreed objectives
- Apply analytical and problem-solving skills to issues of moderate complexity
- Act as a QA subject matter resource and provide guidance or training to colleagues
- Build effective working relationships with cross-functional teams, including Master Data, Regulatory Affairs, Supply Chain, Global Artwork, and QA Management
- MBO or Bachelor’s degree in Life Sciences or a related field, or an equivalent combination of education and experience
- Suitable as an entry-level role for candidates with a Master’s degree in Life Sciences
- Typically 3 years of experience in Quality Assurance, manufacturing, or a related role within the pharmaceutical or medical device industry
- Previous experience in a GMP-regulated environment is preferred but not required
- Fluent in English
- Comfortable travelling to Breda, 2 days per week
- Able to start latest February 1
- A challenging work environment with excellent career development programs.
- You have the opportunity to grow within the company and to fully develop your skills and competences.
- Hybrid position
- Reimbursement of travel expenses.
- The contract will be through Undutchables.
Salarisomschrijving
€4700.00 - €5000.00 monthly
