Quality Auditor
Posted 1 week ago by QCS Staffing
Negotiable
Undetermined
Undetermined
City Of London, England, United Kingdom
Summary: The Quality Auditor role in London involves conducting audits to ensure compliance with SOPs, GMPs, and regulatory requirements in the pharmaceutical industry. The position requires reviewing production and analytical documentation and resolving audit comments with client areas. Candidates with experience in the pharmaceutical or chemical industry, or recent science graduates with a willingness to learn, are encouraged to apply. This is a 6-month contract position within a leading veterinary vaccine development company.
Key Responsibilities:
- Conduct routine audits of data, procedures, equipment, and systems to ensure compliance with SOPs and GMPs.
- Review and approve production and analytical documentation for API, Safety Assessment, or clinical supply lots.
- Communicate and resolve audit comments with client areas.
- Perform audits or inspections of assigned areas or systems under supervision or as part of a team.
Key Skills:
- Experience in the pharmaceutical/chemical industry or government drug-regulatory agency.
- Working knowledge of cGMP regulations.
- Experience in a QA or similar role in a GMP environment is preferred.
- Bachelor’s degree in a relevant science field.
- Willingness to learn and a positive attitude.
Salary (Rate): undetermined
City: City Of London
Country: United Kingdom
Working Arrangements: undetermined
IR35 Status: undetermined
Seniority Level: undetermined
Industry: Other
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!