Analytical Scientist: Method Development & GMP Validation

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

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.