Industry: Pharmaceutical / Radiopharmaceutical
About the Role
For a leading and fast‑growing organization within the pharmaceutical sector, we are seeking a highly skilled QC Analytical Scientist with strong expertise in ICP‑MS. In this role, you will take ownership of the implementation, development, and validation of advanced analytical methods, supporting the quality control of specialized products in a GMP‑regulated environment.
Key Responsibilities
- Lead the implementation and qualification (IQ/OQ/PQ) of ICP‑MS instrumentation within the QC laboratory
- Develop, optimize, and validate ICP‑MS analytical methods
- Perform routine and non‑routine analysis on in‑process samples, final product batches, and raw materials
- Interpret analytical data with a focus on trace elements, impurities, and contamination control
- Troubleshoot and maintain ICP‑MS systems to ensure optimal performance
- Ensure all activities comply with cGMP standards
- Write and maintain SOPs and analytical documentation
- Act as subject matter expert (SME) during audits and inspections
- Collaborate with external laboratories when required
Profile
- Master’s degree in Analytical Chemistry or a related field
- Proven hands‑on experience with ICP‑MS (essential)
- Strong background in method development and validation
- Solid understanding of trace elemental analysis and contamination control
- Experience working in a GMP‑regulated environment is a strong advantage
- Willingness to work with (or learn about) radioactive materials
What’s Offered
- Opportunity to work in a highly specialized and innovative environment
- Exposure to cutting‑edge analytical technologies
- A role with ownership and impact within a growing organization
- Competitive salary and benefits package
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