We are looking for a Senior Chemical Analyst to pick up all non-routine aspects on the QC-lab and to work on improvement processes. Apply now if you're available per 2027 and experienced with Stability, out of specs, deviations, and SOP writing.
Job description
You are working in a relatively small team as a Senior QC Analyst focused on improving the processes and handling non-routine events with the Lab Manager and QA-team. The lab team tests hundreds of raw materials and final products, which means regular method validations, occasional out of specs and deviations and a lot of variety. Outside of the non-routine aspects, you are a senior member of the analytical team and do HPLC, GC, UV, IR, titrations, physical testing, dissolution testing, grain size, and much more. The lab will have many modernization projects over the coming year that you will be heavily involved in, so the time to join is now!
Responsibilities
- Handle deviations and OoS investigations from the QC end
- SOP writing
- Method validation
- Continuous improvement
- Work under GMP guidelines
- Involvement in automation projects and lab improvements
- Chemical analysis using a wide range of techniques
Profile
- BSc or MSc degree in analytical chemistry or another relevant field
- Several years of experience in pharmaceutical QC
- Experience with deviation handling, method validation, SOP writing
Benefits and practical information
- Long term position, start through Oxford
- Salary range: €3800,- to €4800,- gross monthly
- Full-time role on site, 32 hours is possible
- Region: Amsterdam
- Vacaturenummer: 27594
