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Quality Auditor

Quanta Consultancy Services Ltd

City Of London

On-site

GBP 30,000 - 45,000

Full time

30+ days ago

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Job summary

A leading pharmaceutical company is seeking a Quality Auditor for a 6-month contract in London. This key role involves conducting compliance audits and reviewing documentation to ensure regulatory conformity. Ideal candidates will have experience in the pharmaceutical industry and a solid understanding of GMP regulations, or new graduates ready to enter the field.

Qualifications

  • Experience in the pharmaceutical/chemical industry, preferably in a QA role.
  • New graduates considered with willingness to learn.
  • Working knowledge of cGMP regulations is beneficial.

Responsibilities

  • Conduct routine audits of compliance with SOPs and GMPs.
  • Review and approve production and analytical documentation.
  • Communicate and resolve audit comments with client areas.

Skills

Audit Compliance
GMP Regulations
Attention to Detail

Education

Bachelor’s degree

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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