Global Compliance Expert

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Amar Annamalai
Amar Annamalai's picture
Global Compliance Expert

Excellent opportunity for an experienced GCP/PV professional to take on a challenging position working site based in Basel, Switzerland.

In this senior position you will have a broad range of responsibilities focused around the GCP and PV audit function.

Main Responsibilities
*Execute complex GCP/PV compliance activities and some GMP compliance activities
*Escalate based on the audit outcome and monitor actively the CAPA follow-up
*Support inspection readiness of the involved organisations and manage health authority interactions and follow-up
*Training of auditors and site / organisation inspection management capabilities for GCP/PV

In this position you will have
*Auditing experience in PV and GCP
*Broad experience in Pharmaceutical industry
*Experience interacting with major Health Authorities

You will benefit from
*Working in a senior position for a market leading organisation
*Relocation support
*Opportunity to work in an exceptionally experienced group

If you have the skills and experience for this opportunity please email your C.V. to eval(unescape('%64%6f%63%75%6d%65%6e%74%2e%77%72%69%74%65%28%27%3c%61%20%68%72%65%66%3d%22%6d%61%69%6c%74%6f%3a%50%68%69%6c%40%73%74%65%6c%66%6f%78%75%6b%2e%63%6f%6d%22%3e%50%68%69%6c%40%73%74%65%6c%66%6f%78%75%6b%2e%63%6f%6d%3c%2f%61%3e%27%29%3b')) for further details and confidential correspondence

Phil is a Quality Assurance Search expert at Stelfox Pharmaceutical Search covering Europe, UK, North America and Asia

For more updates on great jobs and opportunities follow Phil on twitter - @StelfoxQA

GCP, PV, GMP, Good Clinical Practice, Pharmacovigliance, GVP, Good Vigilance Practice, Good Manufacturing Practice, compliance, audit, auditor, CAPA, Europe, training, Clinical QA, CQA, Quality, Quality Assurance, HA, Health Authority, FDA, EMA, MHRA, QMS, Trackwise, Switzerland, Basel

Deadline: 27 December 2013

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