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Quality Control Analyst

SRG

Liverpool

On-site

GBP 60,000 - 80,000

Full time

12 days ago

Job summary

A prominent global pharmaceutical manufacturer in Liverpool seeks a QC Analyst – Biosafety to join their Quality Control team for a 12-month contract. The role focuses on conducting tests in compliance with GMP guidelines, and is ideal for Biological Science graduates with relevant experience. Key responsibilities include routine testing and proper documentation, while preferable skills include familiarity with cell cultures and laboratory management systems.

Qualifications

  • Experience of working to GMP/pharmaceutical regulatory requirements is desirable.
  • Biological background either from university degree or relevant work in the field.

Responsibilities

  • Performing a range of tests within a highly regulated Quality Control laboratory to GMP regulations.
  • Performing routine QC testing.
  • Documenting laboratory results in an accurate and timely manner.
  • Complying with GMP regulatory requirements at all times.

Skills

Computer skills (Excel, Word, Outlook)

Education

Biological Science degree

Tools

LIMS
SAP

Job description

  • Job Title: QC Analyst – Biosafety
  • Location: Speke, Liverpool.
  • Contract: 12 months
  • Rate: £15.25 p/h (inclusive of shift uplift)
  • Shift: 4 days on, 4 days off. 7am – 7pm.

SRG are currently working with a global pharmaceutical manufacturer based in Liverpool, looking for QC Analyst (Biosafety) to join the team. The site in Speke specialises in the production of sterile injectable products, for the treatment of the flu. This is a fantastic opportunity for a Biological Science graduate with some GMP experience to further their career.

Main responsibilities:

  • Performing a range of tests within a highly regulated Quality Control laboratory to GMP regulations.
  • Performing routine QC testing
  • Documenting laboratory results in an accurate and timely manner.
  • Complying with GMP regulatory requirements at all times.

Key requirements:

  • Experience of working to GMP/pharmaceutical regulatory requirements is desirable.
  • Biological background either from university degree or relevant work in the field
  • Computer skills, excel, word, outlook

Preferrable

  • Experience within cell cultures and/or assay testing.
  • LIMS and SAP
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