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Quality Assurance Officer

United Kingdom, Dinnington · Job Posted June 03, 2026
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Job Description

We have a fantastic opportunity for a Quality Assurance Officer to join our Radiopharmacy Quality Team. If you have experience in Quality Assurance within a GMP environment; good organisation skills; proactive with a can-do attitude; detail-focused and time-oriented; an excellent grasp of problem solving and report writing skills; good at both working on tasks in a team and independently; then this may be the opportunity, you are looking for. The Quality Assurance Officer will be an active member of the Quality Assurance Team, responsible for supporting the QA Manager in overseeing GMP compliance and the effectiveness of the Quality Management Systems supporting the manufacturing, testing and release of the product. Experience in Good Manufacturing Practice (GMP) is essential. Prior experience within a radiopharmaceutical setting is desirable. Validation experience and auditing experience are desirable but not essential.

Job Responsibility

Supporting the QA Manager in overseeing GMP compliance and the effectiveness of the Quality Management Systems supporting the manufacturing, testing and release of the product

Requirements

  • Degree or higher in relevant scientific area (pharmacy, chemistry, or Biology) or equivalent experience in a pharmaceutical setting
  • A strong background in Quality Assurance, preferably with experience in Quality Assurance to produce Sterile injectable products and/or radiopharmaceuticals but is not essential
  • Ideally has a practical experience in activities of quantitative and qualitative analyses of active substances and of the necessary testing and checking to ensure the quality of medicinal products or associated relevant experience
  • Experience of other roles such as Production/QC or QA in a radiopharmaceutical setting would be advantageous but not essential
  • Experienced in Microsoft Windows products (Word, Excel and PowerPoint)
  • First class written and communication skills
  • Good listening skills
  • Excellent interpersonal skills
  • personable
  • Excellent organisation skills
  • Good timekeeping
  • Good attention to detail
  • Self-motivated
  • Able to work on own
  • proactive including both defining and executing tasks
  • Leads by example
  • Good regulatory knowledge (GMP as applicable to sterile manufacture and radiopharmaceuticals)

Nice to have

  • Prior experience within a radiopharmaceutical setting
  • Validation experience
  • auditing experience
  • Experience of other roles such as Production/QC or QA in a radiopharmaceutical setting

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