If you’re looking for a role where scientific precision and regulatory impact come together, this position is worth considering. You will validate and qualify a wide range of laboratory instruments within a GMP‑controlled environment, working closely with internal teams and clients. The work ranges from drafting and executing IQ/OQ/PQ protocols to analysing results, supporting audits and managing documentation. You contribute directly to safe, compliant and reliable processes in highly regulated life‑science settings. For someone who enjoys combining technical depth with structured quality work, this is a logic next step

Your value to the position

Bachelor of master diploma in een Life Sciences georiënteerde opleiding of gelijkwaardig door ervaring

Kennis van relevante regelgeving en normen (GMP, GAMP5, FDA, Pharmacopeia)

Kennis van data integrity is een plus

Vloeiend Nederlands & Engels

What they offer in return

You receive a competitive salary with a broad benefits package, including a company car, iPhone, laptop, meal and eco vouchers, group insurance, hospitalisation coverage, a net expense allowance and a yearly company‑performance bonus. You benefit from 36 days of leave and the option to work from home for a healthy work‑life balance. You grow in a strong learning environment with training through the internal academy and daily support from team leads. A trust‑based team culture with regular meetings and team‑building activities completes the package.

Contact

If you are interested in this position and would like to know more about it, please contact:

Benize Bester, Recruitment Specialist                              Nele Geusens, Recruitment Consultant

T: +31 (0) 6 15 68 69 49                                                       T : + 32 497 57 08 94

E: bester@themagroup.eu                                                 E: geusens@themagroup.eu