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    • Perform routine and non-routine analysis of pharmaceutical finished products, and stability samples using HPLC, GC, Dissolution, and other analytical…
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    • After sampling, specimens must be delivered to our Coventry laboratory,…
    • Up to date with laboratory health and safety procedures.
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    • Reconcile raw materials and ingredients used in compounded products.
    • A keen interest in science.
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    • Perform routine and non-routine analysis of pharmaceutical finished products, and stability samples using HPLC, GC, Dissolution, and other analytical…
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    • Maintaining high standards of health & safety, including COSHH procedures.
    • Has previous school, college or laboratory experience.
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Quality Control Analyst
ACE Laboratories Ltd
·
2.8
London HA8
£26,500 - £28,000 a year
Full-time
Apply now

Job details

Here’s how the job details align with your profile.

Pay

£26,500 - £28,000 a year

Job type

Full-time

Benefits

Pulled from the full job description
Free parking
On-site parking

Full job description

Key Responsibilities

  • Perform routine and non-routine analysis of pharmaceutical finished products, and stability samples using HPLC, GC, Dissolution, and other analytical techniques
  • Ensure all testing is carried out in compliance with GMP, SOPs, and regulatory requirements
  • Accurately document all analytical data, observations, and deviations in accordance with ALCOA+ principles
  • Perform equipment calibration, qualification, and routine maintenance as required
  • Troubleshoot analytical methods and instruments, and escalate issues when necessary
  • Assist in method development and method transfer activities where applicable
  • Support laboratory investigations, OOS, and deviation reports with technical input
  • Provide support and guidance to junior analysts and contribute to their technical development
  • Maintain lab cleanliness, safety, and regulatory compliance at all times

Occasional Duties

  • Perform routine analysis of finished products for physical parameters, including: Average Weight, Uniformity of Weight, Disintegration, Friability, Hardness, Water content by Karl Fischer (KF),Identification tests (chemical, UV, IR),Loss on Drying (LOD), and product Description

Candidate Requirements

Minimum Qualifications & Experience:

  • A relevant science degree (e.g., Chemistry, Pharmaceutical Sciences, Biochemistry, etc.)
  • Minimum of 6* years of experience* in a GMP-regulated pharmaceutical testing laboratory
  • Strong hands-on experience with HPLC, GC, and Dissolution is essential

Essential Skills:

  • Sound understanding of analytical chemistry principles and GMP compliance
  • Familiarity with analytical instruments and software (e.g., Empower, Chromeleon)
  • Good organizational, communication, and problem-solving skills
  • Ability to work independently and collaboratively in a fast-paced environment

Job Type: Full-time

Pay: £26,500.00-£28,000.00 per year

Benefits:

  • Free parking
  • On-site parking

Work Location: In person

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