Analytical Chemical Development Scientist
Eurofins
Job Description
Unfortunately, we are unable to offer visa sponsorship for this role.
This is a full time, 12 Month Fixed Term Contract position, working a flexible 36.5 hour week, Monday – Friday.
The purpose of this role is to provide Analytical support to the client’s drug substance development area from late phase clinical through to commercial development support.
Job Responsibilities
- To perform routine and non‑routine Analytical Testing using a broad range of analytical techniques for regulatory starting materials, intermediates and drug substance including LC, GC, MS, and spectroscopic methodology.
- Support the development and subsequent validation of LC and GC analytical methodology.
- Support any relevant technical troubleshooting activities.
- Ensure work activities are conducted to the highest standards of quality and GMP compliance.
- To identify any opportunities for improvement of quality and service and work with the team to implement continuous improvement.
- To document data as dictated by current client policies and procedures.
- Operate in electronic systems, including electronic notebooks and chromatographic data systems.
- To ensure that all documentation is carried out on time, is accurate and legible and conforms to the relevant quality standards.
- To update any relevant documentation when requested by lead scientist or client representative.
- To participate in the preparation of reports.
About Eurofins
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries to make life and the environment safer, healthier and more sustainable. From the food you eat to the medicines you rely on, Eurofins works with the biggest companies in the world.
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