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Closing date for applications: 31 May 2023

MAC is a full-service global Contract Research Organisation (CRO). We also own a network of research sites. Our mission is to serve with honesty and integrity to make an outstanding contribution to human health.

We’ve an exciting opportunity for a hard-working individual who is capable of working independently and in a team to join our GMP QC team as a GMP QC Inspector at Manchester.

Full-time permanent position.

Main Responsibilities

  • Inspection and approval of clinical trial medicinal products

  • Review of associated documentation

  • Ability to prioritise workload and deal with changes to priorities to support a fast-paced ever changing manufacturing environment

  • Liaise and communicate with multiple departments to facilitate the on-time release of products.

Key Skills and Requirements

  • Good interpersonal skills

  • Very good skills with Microsoft Office (e.g., Word, Excel)

  • The ability to write clear and concise reports

  • Good attention to detail and excellent organisational ability

  • Sufficient initiative to be able to work alone and with a team

  • GMP Production experience would be an advantage

  • Background in Microbiology, Chemistry or similar life science would be an advantage

  • Some experience in a clinical environment would be useful


  • Competitive salary in keeping with pharmaceutical industry standards and will reflect experience

  • Health Insurance

  • Free onsite parking

  • 25 days annual leave (increasing in increments to 30 days after 6 years' service)

  • Your birthday off work

MAC Clinical Research invites applications from highly motivated candidates, with a desire to fulfil their full potential. You will be working with an organisation that sees you as an investment and is keen for you to achieve your career aspirations.

Job Description - GMP QC Inspector
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Salary: Competitive + Negotiable £ Apply Now


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