- Senior International GCP Auditor
Note: This position could be filled in South San Francisco, Welwyn Garden City or Basel
The mission of Genentech Product Development Quality Assurance 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. ...
- Pharmacovigilance Auditor
Interbational Safety Leader required in BasingstokeContact Emma Hobbs on 01483 228190 email@example.com to didcuss further.Under the direction of the Head of QA & PV, this position is responsible for the oversight and conduct of audits in support of the pharmacovigilance system audit plan. The purpose of the role is to provide ongoing assessment and support of safety and risk management activities governed by global and local pharmacovigilance regulations. ...
- **Pharmacovigilance Auditor - PV Background is Ideal**
A very well known and successful Global Pharmaceutical company is seeking a PV Audit professional to join their team, based in the South East of the UK. Ideally, this professional will come from a PV background, and will be motivated by auditing. The company are one of the biggest names in the Global Pharma industry, and can offer a fantastic opportunity to progress through a dynamic team. You will need PV Auditing experience for this role, however there will be constant development offered.
- Quality Auditor (Contract)
12 month contract position for a Quality Auditor in Berkshire offering competitive salary!!
- PV/QA Snr Manager *** The Netherlands - Do you have extensive GCP or Pharmacovigilance experience, and want to move into a Global role?
My client is willing to look at individuals from the broader range of clinical development, with a recent Quality assurance/ compliance experience. If you wish to apply for this role send your CV with a covering note to firstname.lastname@example.org quoting reference number noted above. Alternatively to have a confidential discussion about this or other potential roles or career options, call Theo Moore, in the UK London office, on +44 (0)207 801 3384.
- **EU QPPV Project Lead - Global Pharma Company**
A very well known and successful Pharmaceutical company is seeking an EU QPPV Project Lead for a brand new role within the company. This position will be working alongside the current EU QPPV and will be focused on the Authorization, Development and Management of the PVSMF. As well as this, you will work with the QPPV to improve oversight and work on initiatives with the Global Pharmacovigilance team. The ideal candidate for this will have strong project management and PV skills.
- GCQA Audit Specialist, (Netherlands) – Urgent Contract require
Urgent Contract requirement with a leading Pharmaceutical group. In this role you will support the execution and documentation of study, vendor and system related clinical audits.
- **Associate Director GCP Quality Assurance**
A top pharmaceutical company is actively seeking an Associate Director of GCP Quality Assurance to join their team, ideally based in Warsaw, Poland. The company are one of the most recognizable names within the industry and can offer a fantastic platform for progression. The ideal candidate for this role will be an experienced GCP Auditor, Manager and will have the ability to see the bigger picture within GCP Quality Assurance.