Quality Engineer
HALIX
General information
The Quality Engineer is responsible for supporting both the Quality Control (QC) team and the Quality Assurance (QA) team, in all quality-related activities, ensuring compliance with regulatory standards and internal procedures. The quality engineer is formally part of the QC-team.
- Draft and manage QC-related quality records, including OOS, deviations, CAPAs, and change controls.
- Conduct root cause investigations and ensure timely and effective closure of quality issues.
- Perform peer reviews of executed assay documentation to ensure accuracy and compliance.
- Ensure compliance and completeness of QC SOPs and work instructions.
- Manage all documentation, results and samples with regards to outsources stability programs
- DocController of the eDMS: Manage document records, workflows, etc for all HALIX departments.
- Print hard copies, such as log books.
- Hard copy archival
- Support incoming goods management
- Support assessment of supplier change notifications
- Environmental monitoring of clean rooms
- Testing of water samples
- QA Document control, document issuing, and archiving
- AD hoc QA activities
- MBO/HBO degree in related field.
- A minimum of 2 years of experience in the pharmaceutical and/or biotech, preferably in a quality unit.
- Advanced knowledge of GMP, GDocP and data-integrity.
- Experience in writing quality records
- Experience in reviewing analytical assay documentation
- Good command of English language, both verbally as in writing.
- Excellent technical writing skills.
We are looking for a candidate who is committed to continuous professional development, is analytically strong, and works in a results‑oriented way. You take ownership of your work, plan and organize effectively, and work efficiently toward set goals. Additionally, you are a team player who actively contributes to strong collaboration.
- You will be part of a steadily growing and dynamic biopharmaceutical company offering a great environment for self-starters.
- A culture that is characterized by entrepreneurial spirit and close and transparent communication. The patient’s well-being is always our top priority. This combination is the basis for an interesting and challenging environment.
- You will be working in our dynamic headquarters in Leiden.
- Being part of a company that is focused on excellence in GMP Manufacturing.
- A competitive salary that matches your responsibilities and experience.

