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Analytical Chemical Process Development Scientist Analytical Chemical Process Development Scien

Job in Liverpool, Merseyside, L1, England, UK
Listing for: Job Search Place Limited
Full Time position
Listed on 2026-06-17
Job specializations:
  • Science
    Research Scientist, Data Scientist, Clinical Research, Medical Science
  • Healthcare
    Data Scientist, Clinical Research, Medical Science
Salary/Wage Range or Industry Benchmark: 80000 - 100000 GBP Yearly GBP 80000.00 100000.00 YEAR
Job Description & How to Apply Below
Position: Analytical Chemical Process Development Scientist Analytical Chemical Process Development Scien ...

Analytical Chemical Process Development Scientist

Unfortunately, we are unable to offer visa sponsorship for this role. This is a full time, permanent position working 35 hours per week flexibly between 07:00 - 19:00.

Eurofins PSS is recruiting for an analytical Scientist with a range of experiences from recent Graduates to Experienced Scientists to provide onsite analytical support as a Eurofins Managed PSS Scientist, based at the Bristol Myers Squibb Moreton facility in the Wirral.

This position is a fully employed Analytical Scientist by Eurofins PSS, supporting services delivered to our client on their site.

This role is not employment with Bristol Myers Squibb and Bristol Myers Squibb does not manage the recruitment or employment terms for this position.

As an Analytical Scientist your role will be to perform method development and proof of concept method validation analysis across a range of pharmaceutical raw materials, intermediates and drug substances, produce accurate results within an acceptable timeframe.

Job Responsibilities that you will be covering
  • You will perform routine and non-routine analysis of pharmaceutical products using a range of analytical techniques (primarily HPLC, GC and MS).
  • You will support technology transfers for new products entering the team, ensuring smooth implementation and alignment with client procedures.
  • You will review analytical data for GMP compliance and initiate or follow up on OOS results and action limits when required.
  • You will document data in accordance with current client policies and procedures and prepare/approve results for tests in which you are trained and deemed competent.
  • You will maintain productivity through agreed metrics (e.g. test numbers, cycle times) and support audits, method revisions, and testing of QC samples.
  • You will liaise with client representatives, provide updates to designated personnel, support continuous improvement initiatives, and work flexibly in line with business needs.
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