- Senior Quality Assurance Associate (GCP)
TMQA is an international Quality Assurance consultancy company with headquarters in Scotland and Slovakia. We are seeking an experienced GCP auditor to join our expanding team.
- Senior Manager Pharmacovigilance Quality Assurance Auditor
The role of the Senior Manager, Pharmacovigilance Quality Assurance is to provide a variety of Quality Assurance (‘QA’) services to external clients. Of most relevance will be experience of conducting audits in pharmacovigilance.
- **Senior GCP Auditor - UK, Switzerland or USA!**
A very well known and successful Global pharmaceutical company is seeking a Senior GCP Audit professional to join the expanding team. This is a brand new position, created due to the progress of the group and requirement for extra resource. Ideally, the select candidate will have experience in Corporate Auditing, Process and System Auditing and also PV working knowledge. This opportunity can really provide a platform for progression within a Global organisation.
- **Senior GCP Auditor, CONTRACT Opportunity - Ad Hoc Audits - Based ANYWHERE Globally!**
I am working with a very successful and recognised Bio-pharmaceutical company who are seeking GCP Auditors to work for them on Audits on an Ad-Hoc basis. Due to the exciting growth of the company, these audits are ever increasing in number and the locations are truly variable. This is why my client needs strong contractors to conduct these audits on a regular basis.
- Senior Auditor QA
Senior QA Auditor
Salary: Up to £25,000 plus benefits depending on experience
- 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 - 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.
- **CONTRACT PV Auditor - South East UK**
A well known and successful Global Pharmaceutical company is seeking a PV Audit professional on a Contract basis, to be based from the South East of the UK. This position is to cover a permanent professional who is being utilised in another area of the business. The contract will be effectively a 5 days per week contract, also with the possibility to make the position permanent at the end, should you want. You will have conducted PV Audits on an international level.
- **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.
- Site GXP Compliance Manager Munich
GXP Compliance role for growing pharma client