Analytical Chemist

JR United Kingdom; East Midlands; On-site; GBP 30,000 - 40,000; Full time

Job summary

A leading CDMO in the UK is seeking an Analytical Chemist. Join a dynamic R&D team focused on developing next-generation therapies. Responsibilities include conducting analytical tests, ensuring GMP compliance, and supporting method development. Ideal candidates have a degree in Biochemistry or Chemistry and knowledge of HPLC. Experience in pharmaceutical product testing is preferred. This position offers a chance to significantly impact global health.

Qualifications

• Industry experience in pharmaceutical product testing preferred.
• Hands-on lab experience is necessary.
• Comfortable with statistical methods and experimental design.

Responsibilities

• Conduct analytical testing on pharmaceutical products.
• Support the design of testing protocols for data output.
• Prepare laboratory and quality incident reports.
• Represent the lab in internal and external meetings.
• Uphold safety culture and report incidents appropriately.
• Complete CAPA within defined timelines.

Skills

Analytical testing

GMP compliance

HPLC

Good understanding of GMP and GLP

Education

Degree in Biochemistry or Chemistry

Tools

GC

MS

UPLC

UV

Job description

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Are you passionate about science and want to make a tangible impact on global health?

Looking for your next position as an Analytical Chemist?

We're recruiting on behalf of a leading CDMO that develops and manufactures life-saving drug-device combination products. Their UK site is expanding, and we are looking for additional Analytical Scientists with a background in pharmaceutical testing (or freshly graduated) to join their dynamic team.

The Opportunity

This is a fantastic opportunity to be part of an R&D team developing next-generation therapies. You’ll work in a GMP-compliant environment, contributing to analytical testing, method development, and product innovation, all while ensuring the highest standards of quality and safety.

Key Responsibilities

• Conduct analytical testing on pharmaceutical products, ensuring compliance with GMP standards.
• Support the design of testing protocols to drive robust, high-quality data output.
• Prepare laboratory and quality incident reports as needed.
• Represent the lab in internal and external meetings, including with regulatory bodies.
• Uphold a strong “safety-first” culture and report incidents appropriately.
• Complete CAPA (Corrective and Preventative Actions) within defined timelines.

Your Profile:

• Ideal: Industry experience in pharmaceutical product testing
• Degree-qualified in a relevant scientific discipline with hands-on lab experience (Biochemistry or Chemistry)
• Solid knowledge of HPLC is essential; experience with GC, MS, UPLC, or UV is advantageous.
• Good understanding of GMP, GLP, and method development principles.
• Comfortable with statistical methods and experimental design.

Currently looking for your next step in the field? This offer could be the right one for you!

Click the link to apply directly, and we aim to be in touch within the next 2 working days!