- **GLOBAL QUALITY ASSURANCE PV AUDITOR - GERMANY - WORLDWIDE COMPANY**
My client is a world renowned pharmaceutical company with products being sold right across the globe, helping over 400 million people tackle everyday aliments and have been stocking medicine cabinets for the past 25 years. The role my client is looking to recruit for is a PV auditor, who can truly be a worldwide ambassador while auditing at various sites within the company network.
- ** SENIOR PV AUDITOR - GERMANY - HIRING NOW!!!!**
My client is a worldwide reaching client who's products form an important cornerstone of the treatment of patients with rare diseases. They strive to maintain their status as the market leader in their chosen therapeutic areas. They are seeking an experienced PV Auditor to join their operations within an expanding Quality Assurance team. This opportunity is perfect for an individual who has a real desire and expertise within Pharmacovigilance.
- Pharmacovigilance Snr Manager or Associate Director - Take the lead in a new PV/QA Initiative - Great Salary, Bonus & full Re-location Package
This role can be positioned at either Snr Manager or Associate Director level and comes with a great salary, bonus and full relocation package available where necessary. If you wish to apply for this role send your CV to firstname.lastname@example.org or call Theo Moore or Matt Grieg in the UK London office, on +44 (0)207 801 3380
- Pharmacovigilance Snr Manager / Specialist - Provide PV inspection support from the EU & Head office - The Netherlands
My client who are a rapidly expanding organisation who have developed their R&D portfolio through a mixture of product innovation and successful International market maximisation over the last 5 years.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 call Theo Moore on +44 (0)207 801 3380.
- *** Manager / Sr. Manager Clinical Quality Assurance – GVP/PV *** Netherlands *** Cover GCP & Pharmacovigilance in an exciting high-impact role ***
*** Manager / Sr. Manager Clinical Quality Assurance – GVP/PV *** Netherlands *** Cover GCP & Pharmacovigilance in an exciting high-impact role ***
Contact Theo Moore or Matt Grieg via e-mail on CV@advregulatory.com or call +44(0)207-801.33.80
- Pharmacovigilance QA Professional
This is a role focused on pharmacovigilance related quality and compliance activities.
- PV Consultant - Exciting QA Consultancy, UK
A very interesting and exciting client of mine is actively seeking a PV Consultant to join their growing team, ideally based in the UK. This opportunity is for a PV Audit or Management professional to progress alongside a developing company, whilst also improving their knowledge and experience in this ever changing and varied environment. Ideally, you will have PV Audit experience on a Global basis and enjoy travel.
- PV Strategy Manager/Sr Manager
The PV Strategy Leads are responsible for the development and implementation of a risk-based quality assurance strategy that covers all PV processes and activities performed by Pharma global functions, Affiliates, service providers and licensing partners. This role conducts risk assessment to deliver an audit program, provides strategic direction to audit operations, and provide actionable data to senior management based on analysis of compliance data and identification of trends. ...
- PV Scientist Level 1 - ICSR Management
You will be accountable for providing molecule-driven support for ICSRs, including the processing of high quality, accurate and medically cohesive ICSRs in line with regulatory and company timelines and requirements as well as other activities supporting the ICSR process.
Your primary responsibilities and accountabilities are as follows:
Accountable for processing high quality, accurate and medically cohesive ICSRs in line with regulatory and company timelines and requirements. ...
- Safety Scientist
This position is primarily responsible for supporting all operational functions within the Safety Department including, but not limited to, client interface and deliverables, individual case safety report (ICSR) case processing; assisting with project start-up: process flows; assist with database configuration needs; training and contributing to the development and maintenance of departmental standards (SOPs) and guidelines.