Location: QPS, Groningen, NL (onsite role)
Company: QPS Netherlands BV in Groningen is part of a global organization that conducts drug research for international pharmaceutical and biotechnology companies.
Responsibilities- Lead projects and manage the execution of studies according to plan and budget.
- Work in the laboratory, managing assays and ensuring technical quality.
- Anticipate changes to study plans and handle deviations in accordance with the quality system.
- Serve as the single point of contact for clients, collaborating closely with scientists, technicians, and the team lead.
- Contribute to the development of new medicines.
- Process data from analysis and communicate results to sponsors.
- Search scientific literature and stay up to date with the latest developments.
- Ensure studies comply with GLP/GCP regulations and quality system guidelines.
- PhD in bioanalysis, chemistry, biochemistry, or a comparable field, or a master’s degree with equivalent laboratory experience.
- Hands‑on experience executing, developing and validating biochemical and immunological techniques such as ELISA, ECL, FACS, enzyme assays and cell‑based assays, preferably within a GLP environment.
- Proactive, excellent analytical skills and capacity to work well under pressure.
- Experience managing projects and familiarity with quality guidelines according to GLP/GMP.
- Strong communication skills; proficient in Dutch and English, both written and oral.
- Based in the Netherlands and able to work on‑site in Groningen.
- Great learning opportunities with seasoned professionals supporting career development.
- Full‑time position (40 hours per week) within the dynamic environment of a global organization focused on improving human health and quality of life.
- A collaborative team environment that values diversity, creativity, and challenge.
Salarisomschrijving
€50000 - €70000 monthly