Key responsibilities:
- Review and approve SAP Master Data activities, including critical value verification and Bill of Materials.
- Review and approve artwork for medical products.
- Create and update operational SOPs and Work Instructions.
- Perform QA reviews and support QA related projects when required.
- Assist with investigations and data integrity activities.
- Ensure compliance with GMP and other regulatory standards.
- Identify, analyze, and help resolve quality or data-related issues.
- Collaborate with cross-functional teams and provide guidance when needed.
- Bachelor's degree in Life Sciences or a related field.
- This position is also suitable as an entry-level opportunity for candidates with a Master's degree in Life Sciences, etc.
- Previous experience with GMP/pharmaceutical environments is preferred.
- Around 3 years of experience within QA, manufacturing, pharmaceutical, or medical device environments is an advantage.
- Strong attention to detail and an accurate working style.
- Good communication and interpersonal skills.
- Ability to work independently and under pressure, as well as to work with technical information and quality documentation.
- Analytical and problem-solving mindset.
- Fluent in English.
- A challenging work environment with excellent career development programs.
- A competitive salary package.
- 30 Holidays.
- Reimbursement of travel expenses is dependable on travel distance.
- The contract will be through Undutchables.
Salarisomschrijving
€4780 - €4780 monthly