Analytical Scientist
Eurofins
Liverpool, United Kingdom
Job Description
The purpose of this job is to perform stability testing of finished pharmaceutical products and produce accurate results within an acceptable timeframe.
- To perform routine and non-routine analysis using traditional and modern analytical techniques (primarily: HPLC, Dissolution and Karl Fisher determination), as required by the client’s representative.
- To perform technology transfers on new products entering the team.
- To review analytical data for GMP compliance.
- To initiate and follow-up OOS results and action limits as per client procedures.
- To document data as dictated by current client policies and procedures.
- To collect and measure productivity through agreed metrics such as number of tests performed, cycle times, lab/product issues, number of hours worked per project, etc.
- To prepare and approve results for tests in which they have received the appropriate training and are deemed competent.
- To deal with client queries and contact designated personnel, with appropriate support from onsite leadership, with any relevant information or issues relating to test results or the service in general.
- To keep up to date with any technological or method revisions in their area, ensuring their training is complete and adjusting their work as required with approval from the Lead Analyst.
- Support local audits as required.
- To perform testing of QC samples in accordance with client procedures.
- To revise SOPs as required.
- To adhere to all client standards in the areas of safety, housekeeping and quality, notifying management of any discrepancies.
Qualifications
- A degree in Chemistry or a related discipline is required.
- A sound, fundamental knowledge of Chemistry is essential, with knowledge of Analytical techniques highly desireable.
- A minimum of 1 year relevant experience of analysis in a pharmaceutical testing laboratory (preferably with exposure to solid dose products) , or equivalent, is desired.
- The candidate should be experienced and competent with traditional analytical techniques as well as modern instrumental equipment (HPLC, Dissolution, Karl Fischer and UV spectroscopy).
- Experience in technology transfers desirable but not essential.
- Must be able interpret raw data and draw conclusions regarding troubleshooting of analyses, instruments and methods.
- Have a thorough understanding of chromatographic techniques.
- Must posses experience of, or have a thorough understanding of working in a GMP environment.
- Must possess the ability to quickly learn new processes.
- Be capable of working proactively to offer suggestions for new ways to improve existing processes.
- Should have the ability to work using paperless systems such as Electronic laboratory notebooks and LIMS.
- Must be competent with MS Office suite of applications.
- Requires the ability to form strong working relationships with colleagues.
- Must have the ability to work on their own initiative and be capable of developing solutions to problems as part of a team.
- Must be willing to operate in a flexible manner and be able to switch priorities at short notice.
- Should seek new ideas to make improvements within own area of control.
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