Analytical Chemical Process Development Scientist Analytical Chemical Process Development Scien[...]

Seeds Renewables; Liverpool; On-site; GBP 30,000 - 45,000; Full time

Job summary

Eurofins is seeking an Analytical Chemical Process Development Scientist in Liverpool, England. This full-time position requires performing method development, routine and non-routine analysis of pharmaceutical products. Responsibilities include using techniques like HPLC, GC, and MS, ensuring compliance with GMP, and liaising with client representatives. Ideal candidates will have experience in analytical methods and a strong attention to detail. Join Eurofins to contribute to innovative pharmaceutical solutions.

Qualifications

• Experience in routine and non-routine analysis of pharmaceutical products.
• Ability to perform method development and validation for pharmaceutical raw materials.
• Strong understanding of analytical techniques including HPLC, GC, and MS.

Responsibilities

• Perform routine and non-routine analysis of pharmaceutical products.
• Support technology transfers for new products.
• Review analytical data for GMP compliance.
• Document data according to client policies.
• Maintain productivity through agreed metrics.
• Liaise with client representatives and support continuous improvement.

Skills

HPLC

GC

MS

GMP compliance

Job description

Analytical Chemical Process Development Scientist

Eurofins

2 days ago

Job Description

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 on site 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.