Take on a senior QC role in a GMP environment in Barneveld, performing varied analyses and investigating deviations. HLO-level education in Analytical Chemistry and extensive GMP experience are required; full-time availability is preferred.
The role
At our client company, you will work as a Senior Chemical Analyst in a pharmaceutical production environment operating under GMP requirements. You will be the first point of contact on the QC floor for deviations and root-cause investigations. You will act as a sounding board for the QC Manager and translate quality objectives into day-to-day practice.
You will also analyse raw materials, intermediates and finished products. The variety of products and analytical methods makes the work varied, with accuracy and flexibility essential.
What you will do
- Perform qualitative and quantitative analyses using techniques such as HPLC, UV/VIS, titrations and wet chemistry.
- Review analytical results.
- Prepare, perform and report analyses in accordance with GMP procedures.
- Identify and investigate deviations, and contribute to OOS/OOT investigations.
- Calibrate and maintain laboratory equipment, and troubleshoot faults.
- Contribute to improvements in analytical methods and processes.
- Train fellow analysts to prepare deviation, CAPA and Change Control documentation.
- Work with QA and production teams.
What we are looking for
- At least HLO-level education and competence in Analytical Chemistry.
- Extensive experience in a GMP environment; supervisory duties or experience as a senior analyst or specialist is preferred.
- Excellent command of HPLC and wet-chemistry techniques.
- You are decisive, communicate effectively and have natural authority.
- You are proactive, have a Quality Assurance mindset and document work carefully.
- Good command of Dutch.
Schedule and offer
Full-time availability is preferred. Working hours, shift pattern and contract details are not specified.
The offer includes a market-rate salary and good secondary employment benefits. Training and further development in GMP and analytical techniques are available. You will join a collaborative team focused on quality, cooperation and professional skill.