Location: Warsaw, Poland (Fully Site based)
Working Hours: Monday–Friday, 8:00am–4:00pm (Some flexibility for later finishes may be occasionally required)
About the Role
We are looking for a Project QC Chemist to join a busy Quality Control team within a pharmaceutical environment. This role focuses on improving and maintaining analytical testing methods, with existing methods already in place. The successful candidate will play a key role in method optimisation, development-related activities, and ensuring analytical robustness.
Key Responsibilities
- Work as part of the QC laboratory team, supporting routine and project-based activities
- Optimise and improve existing analytical testing methods
- Perform analytical method development, verification, and validation
- Support QC documentation, data review, and technical reports
- Ensure laboratory activities are performed in line with site procedures and quality standards
- Collaborate with cross-functional teams including QA, Production, and Technical functions
Skills & Experience Required
- Degree or equivalent experience in Analytical Chemistry, or related discipline
- Experience with method development, verification, and validation
- Strong hands-on experience with HPLC and/or GC
- Background in a pharmaceutical analytical laboratory environment
- Knowledge of GMP is preferred
- Detail-oriented with strong problem-solving and analytical skills
What’s on Offer
- Standard daytime working hours (8am–4pm, Monday–Friday)
- Opportunity to work on technically interesting QC projects
- Stable role within a regulated pharmaceutical environment
If you are an experienced analytical chemist with a passion for method development and continuous improvement in QC, we would welcome your application.