Analytical Method development under GMP - Contract 6 months
Are you a motivated BSc Chemistry or experienced Lab Technician ready to take on more responsibility? Do you thrive in a regulated environment where your analytical mindset and initiative truly matter? Then we have something exciting for you.
We’re looking for a hands-on QC Specialist to join a high-impact team focused on introducing new raw materials into the Quality Control lab. Here, you won’t just follow SOPs—you’ll help write them.
What You’ll Lead
* Be the project lead for method development and method validation—take ownership from concept to execution
* Shape specifications and testing plans for raw materials and help implement new testing methods
* Manage cross-functional collaborations with stakeholders from development, QC, and external testing labs
* Drive changes proactively: from pharmacopeial updates to continuous improvement projects
What You’ll Work With
* Classic wet chemistry techniques and modern tools like HPLC, UPLC, and GC
* GMP-compliant workflows in a fast-paced, innovative pharma environment
* Compendial methods (Ph. Eur, USP, JP) and real-world material assessments
✅ What You Bring
* BSc in Chemistry or Life Sciences or education as Laboratory Technician (CFC)
* 2–3 years of GMP experience (a must!)
* A drive to learn, grow, and contribute to technical leadership in QC
* Proficiency in French and English required
Why Join?
This is not your average lab job. You’ll play a key role in ensuring new product quality at a major pharma site. If you’re ready to take your analytical skills and apply them in a leadership-minded context, we’d love to meet you.
Ready to level up your lab career? Apply now and lead the next generation of raw material introduction!