The latest Auditor jobs - BETA

GCP Auditor with a Fantastic Organisation



A renowned organisation with continued expansion and strong pipeline are looking for a Senior GCP Compliance auditor to join a growing team. This is a highly successful company where there is a real chance to progress your career within Clinical Quality Assurance.

*** Senior GCP Auditor – Flexible Location *** Great Career development opportunity within top 5 Pharma environment. Please contact Marc Van de Voorde on +41-41-710.51.00 - +44-207.801.33.85 marc@advregulatory.com or cv@advregulatory.Com

Homebased GCP Auditor Position- Expanding Organisation



On behalf of a CRO who are currently active in Europe and growing internationally, I am recruiting a Senior GCP Auditor. This is a highly visible role within the company and department, where there is the flexibility of being homebased- or working from one of this organisations offices within the EU.

An outstanding opportunity to join one of the worlds leading contract research organizations and be part of a dynamic and growing international company. Join PRA as a Quality Assurance Auditor and help realize your career potential.

Job summary • QA Auditor required for Global Pharma in Wavre, Belgium • Candidates must speak fluent English • Contract initially for 6 months, contract likely to be extended • Freelancers welcome to apply

As a Clinical Auditor you will responsible for the independent planning and conducting of audits several key clients across the business.

If you are looking to join an organisation with continuing career progression, excellent benefits and the chance to grow with your role this is an excellent position for you. One of the current Assistant Director of Quality Assurance joined this organisation as a Clinical Trials Auditor. The role can be based in any of their European Offices.

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!).

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

A new role to commence immediately with our client. They are looking to recruit a Senior Auditor Regulatory Conformance for their Dublin based offices.

inVentiv Health Clinical, formerly PharmaNet/i3, is a leading provider of global drug development services to pharmaceutical, biotechnology, generic drug, and medical device companies. With 7,000 employees in more than 36 countries, inVentiv Health Clinical offers therapeutically specialized capabilities for all phases of clinical development, bioanalytical services, and strategic resourcing from a single clinical professional to an entire functional team.

Our client is currently seeking a Senior Clinical QA Auditor for their Cambridgeshire location

JOB ROLE:
Our client requires someone with GMP expertise to lead the audit program, planning and executing and following up site, process, vendor and documentation audits.

You will also be expected to plan, conduct and follow-up investigator site audits, process audits, vendor audits and documentation audits. ...

My client is a multi-national CRO headquartered in the UK, seeking a Clinical Quality Auditor to work in a field-based role in mainland Europe.

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.

Senior level opportunity within Quality Assurance for one of the fastest growing Clinical Research Organisations.

GCP Auditor Top 10 Pharmaceutical Berkshire/M4 Corridor If you wish to receive more information regarding this role and organisation please feel free to enquire. This leading Pharma are ideally looking for somebody from a Clinical background with GCP auditing experience. The position will see you carry out the preparation and performing of audits and make sure that regulatory compliance is adhered to.

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, French and German speaking candidates should call Marc Van de Voorde in our Swiss office, on +41 (0)78 170 4042 and for candidates from the UK, NL and rest of world call Mark Twigden, in the UK London office, on +44 (0)207 801 3383.

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.

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, French and German speaking candidates should call Marc Van de Voorde in our Swiss office, on +41 (0)78 170 4042 and for candidates from the UK, NL and rest of world call Mark Twigden, in the UK London office, on +44 (0)207 801 3383.