The mission of Roche Product Development Quality is to provide assurance that non-clinical, clinical and pharmacovigilance activities are conducted in compliance with regulations and guidelines, and to partner with our customers to provide a quality framework that protects patient safety and the company’s license to operate.
Quality Assurance Auditor - France (Marseille) - Freelance Contract!
ClinTec International is actively recruiting for a Contract Quality Assurance Auditor to join our expanding global company in France. The successful individual must be available to conduct a 3-day Audit in September 2014. ...
I am working with a very interesting and advanced Biopharmaceutical company, who are actively seeking a Director of Pharmacovigilance, QPPV, to join their team, based in the UK. The ideal professional must be a Medical Doctor, and have had at least 3 years experience as a QPPV. The company have a very interesting portfolio of products and have shown excellent progress over the past few years. They really are a bright prospect.
If you wish to apply for this role send your CV with a covering note to email@example.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.
If you wish to apply for this role send your CV to firstname.lastname@example.org or call Theo Moore or Matt Greig in the London office on +44 (0)207 801 3380 - or Marc Van de Voorde in our Swiss office, on +41 41 710 5100
I am working with one of the most reputable and exciting Biopharmaceutical companies globally to recruit an Associate Manager for Drug Safety and Risk Management, to be based from their South East Headquarters in the UK. The ideal professional will have a Drug Safety/Pharmacovigilance background and will be experiences within Risk Management. They will also have project leading expertise. As well as this, you will also have some active management experience.
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 email@example.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.
I am currently working with one of the most exciting and progressing Biopharmaceutical companies globally to recruit a Senior Manager for their Quality Assurance Team. This professional will have oversight of the GCP and PV QA operations and will provide expert analysis on where the teams can move forwards. The ideal candidate will be an experienced GCP/PV professional, ideally with auditing experience in both areas. Management experience is also advantageous.
I have been approached by one of the leading names within the Pharmaceutical industry who are actively seeking a Senior Quality Assurance professional for a QA Manager opportunity within their GCP set up. The ideal professional will have extensive auditing experience and will be a reputable professional within the industry. The role will suit a Senior/Principal Auditor who is looking to move up and away from specific Auditing responsibilities and into an oversight position.
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