GMP Analytical Scientist - Drug Testing & Validation

Career Choices Dewis Gyrfa Ltd

Moreton

On-site

GBP 35,000 - 48,000

Full time

12 days ago

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Job summary

Synergy is seeking an Analytical Scientist to join our expanding team in state-of-the-art laboratories in Moreton, UK. The role focuses on analytical testing of drug substances, intermediates and finished medicines in a regulated GMP environment, working closely with customer scientists and lab leads.

You will perform analyses using HPLC, Karl Fischer and dissolution testing, contribute to method development and validation, and ensure compliant documentation in line with cGMP and ALCOA+

Qualifications

  • Hands-on experience with HPLC and other analytical techniques.
  • Proven experience working within a GMP laboratory environment.
  • Strong communication and relationship-building skills.
  • Customer-focused mindset and ability to work in a fast-paced setting.

Responsibilities

  • Analytical Testing & Laboratory Work Plan and perform analytical testing in line with GMP requirements using HPLC, Karl Fischer, and Dissolution testing.
  • Additional analytical techniques as required.
  • Support analytical investigations and troubleshoot technical issues.
  • Contribute to method development, evaluation, and validation activities.
  • Ensure accurate, compliant documentation aligned with cGMP and ALCOA+ principles.

Skills

HPLC
Analytical techniques
GMP laboratory experience
Customer-focused
Strong communication

Education

Degree in Chemistry/Analytical Chemistry/Biochemistry

Tools

Karl Fischer

Job description

Synergy is seeking an Analytical Scientist to join our expanding team in state-of-the-art laboratories in Moreton, UK. The role focuses on analytical testing of drug substances, intermediates and finished medicines in a regulated GMP environment, working closely with customer scientists and lab leads.

You will perform analyses using HPLC, Karl Fischer and dissolution testing, contribute to method development and validation, and ensure compliant documentation in line with cGMP and ALCOA+

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