The latest Auditor jobs - BETA

Seeking Auditors within the Medical Devices sector, to work for Notified Bodies or Medical Device manufacturers themselves. Travel locally, regionally, and internationally. Areas of expertise - Medical Device products and including validation of Microbiology & Sterilisation processes, as well as active Medical Devices.

My Client are looking to add to their current Quality Management team by recruiting a Senior Quality System Specialist / Internal Auditor to work on leading the corrective action and internal audit programs in order to maintain compliance with worldwide quality and regulatory requirements and to promote and drive process and quality improvement.

A global pharmaceutical organisation based in the North Home Counties is seeking a QA Associate for a 6 month contract.

Under general direction of the Senior Manager QA, The QA officer will be responsible for the maintenance of the Quality Assurance activities and the Quality Management System (QMS). ...

An exciting opportunity has arisen to work in one of the most exciting areas of modern medicine within an innovative pharmaceutical company.

My client is currently recruiting for a GCP Compliance Manager to join a successful and growing global Biotech. You will be responsible for the compliance and QA activities within Europe. This is an excellent opportunity to join a company that offers excellent rewards to its employees and as great working environment.

Great permanent senior opportunity - Global QA GMP Auditor for Microbiology - based in Germany , in an international, global pharmaceutical company.
Qualifications Experience: min. 8 years experience in the pharmaceutical or biopharmaceutical industry, e.g. in Pharma Production, Quality Assurance, Quality Control, Development, Audit experience desirable
-Prior Auditing experience desirable For more information's please contact directly with Agness +44 02072556665

Compliance Auditor Sind Sie ein außergewöhnliches Compliance Auditor auf der Suche nach einem neuen Projekt? Clinical Professionals hat eine 1-Jahr befristeten Vertrag in der Schweiz bietet außergewöhnliche Tagegeld, Reisen, Private Krankenversicherung, 28 Tage Urlaub und Überstunden als Option, Hotel-und wettbewerbsfähige Vergütung für diese neue Position.

If you wish to apply for this role send your CV with a covering note to cv@advregulatory.com quoting reference number noted above. Alternatively to have a confidential discussion about this or other potential roles or career options, call Mark Twigden, in the UK London office, on +44 (0)207 801 3383.

Permanent role - PV Auditor - Skills: Principle Auditor to Senior Manager level

Senior Quality Assurance Auditor is responsible for conducting audits of on-going clinical research and data management projects, as well as assisting with handling other QA program initiatives.

About the role This is your chance to join world leader in the healthcare industry. A truly global company, with manufacturing plants across the world- this role can be based in any major city within Europe! Best of all, in this role- you will have the opportunity to see the world while you work (expenses paid!).

Opportunity within Quality Assurance for one of the fastest growing Clinical Research Organisations.

I am working alongside a new and very interesting Pharmaceutical company who are seeking a Senior GCP/PV Auditor to join their expanding and developing Quality Assurance division. This is a brilliant opportunity to join a small and personable company who are looking to grow their operations and being a part of this team now will bring opportunities to progress and achieve more from within.

I have opportunities available for Quality Assurance Professionals to join a market leading Pharmaceutical company in an ever expanding and achieving QA division. I am looking for motivated and driven GCP Auditors who are focused and love what they do! This opportunity is in the South East of England, West of London.

Home Based across Europe are available. Must have GCP audit experience. Competitive salaries. Immediate start.

This is a great opportunity for a Quality Assurance junior to take the next step in their path and turn GLP experience into GCP auditing. If you wish to apply for this role send your CV with a covering note to cv@advregulatory.com quoting reference number noted above. Alternatively to have a confidential discussion about this call Mark Twigden, in the UK London office, on +44 (0)207 801 3383.

Become a GCP Auditor with a growing pharmaceutical company. Our client is looking to fill a role in their excellent QA department. If you wish to apply for this role send your CV with a covering note to cv@advregulatory.com quoting reference number noted above. Alternatively to have a confidential discussion about this or other potential roles or career options, call Mark Twigden, in the UK London office, on +44 (0)207 801 3383.