Quality Auditor

confidential; London; On-site; GBP 35,000 - 50,000; Full time

Job summary

A leading pharmaceutical company in London is seeking a Quality Auditor on a 6-month contract. The role involves conducting audits to ensure compliance with SOPs and GMPs, reviewing documentation, and collaborating with client areas. Ideal candidates will have a background in the pharmaceutical industry or be new graduates with a keen attitude to learn.

Qualifications

• Bachelor's degree minimum required, with a preference for new science graduates.
• Experience in QA, GMP, or relevant regulatory agency is desired.

Responsibilities

• Conduct routine audits of data, procedures, and systems to ensure compliance.
• Review and approve production and analytical documentation according to regulations.
• Perform audits of assigned areas under supervision.

Skills

Attention to detail

Auditing

Compliance

Education

Bachelor's degree or higher

Job description

Quality Auditor - UK, London - 6 Month Contract

Do you want to be involved with exciting pharmaceutical projects?

When it comes to the development and production of veterinary vaccines, our pharmaceutical client has the largest centre in the industry worldwide and is a Centre of Excellence; employing more than 1000 people. They are looking to add to their team and require a Quality Auditor.

Essential Duties and Responsibilities for this role include, but are not limited to, the following:

• The Quality Auditor conducts routine audits of data, information, procedures, equipment, and systems (including computer systems), and/or facilities to ensure the compliance with SOPs and GMPs and worldwide regulations.
• Review and approve production and analytical documentation accompanying the release of API, Safety Assessment, or clinical supply lots (bulk and packaged) to ensure conformance to appropriate regulatory requirements.
• In addition, the Auditor communicates and resolves audit comments with client areas.
• Under supervision, or as part of a team, perform audits or inspections of assigned areas or systems to assess compliance with regulatory and Company standards

Desirable Experience:

• Experience should be in the pharmaceutical/chemical industry or government drug-regulatory agency with a working knowledge of cGMP regulations.
• Ideally you should have existing experience in a QA or similar role in a GMP environment, however we would be just as interested in new science graduates (bachelor's degree minimum) with the right attitude and a willingness to learn.

If this role is of interest to you, please apply now!
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