As a Quality Assurance Associate, you will support QA activities related to SAP Master Data and...
As a Quality Assurance Associate, you will support QA activities related to SAP Master Data and artwork approval within a highly regulated pharmaceutical environment. You will work closely with different international departments to ensure quality standards and compliance are maintained.
Key responsibilities:
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.
Requirements
- Degree in Life Sciences or a related field.
- 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.
Benefits
- 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.