Director of Pharmacovigilance QA Low travel, varied role Consider home-based if you will travel 30%

Recruiter
Advanced Regulatory
Location
Bedfordshire
Posted
02 Feb 2018
Closes
16 Feb 2018
Sector
Healthcare
Contract Type
Permanent
Hours
Full Time
My client offers a merit-based advanced environment for progressive career applicants that want to make their mark in a global R&D and marketed products QA function. The company are investing a very healthy 23% of T/O for their R&D programmes, across 4 therapeutic streams, and can either an office based role in the West of London / M4/M25/M40 corridor or if you are further away, some home working flexibility (plus travel for audit and meetings). Please consider the following for this role:- Would you like to work in a corporate drug development and research based pharmaceutical company, and be visible and supported for your Quality advisory? Are you looking for a role where you are part of the senior team to review and assess Risk, co-develop the audit plan and implement in a mix internal / vendor audit model? Are you someone who wants to be involved with the therapy groups, often by data review, to support the business, and be able to, with integrity, sign off on new products which are highly innovative, often mAb/fAbs, and where there is high unmet medical need? Would you like to work with sites and business systems, to provide QA support for Drug Safety systems and new processes? Do you want to ‘audits’ but not spend more than 30% of your time on the road? Are you looking to work in a team which has a merit based advanced systems and where your ideas matter? ______________________________________________________________________________________________ We would welcome hearing from anyone who would like to be considered for this role, and has existing QA Pharmacovigilance experience, or ICH GCP and CSV with some exposure to PhV audits or inspections or systems. This role is not a CSV role but we are seeking someone who is happy working with both clinical / observational data and systems. The company offers a relocation policy for each country, as well as a strong package, including Stock, RSUs, Bonus, Car and progressive salary banding. The leader of the group has a strong reputation for developing people and is not new to people management. We like the line manager's quality vision, so why not call me in confidence and I will explain who my role is for and her vision, approach and requirements. To apply for this role, please contact me, Matt Greig, at Advanced Regulatory on +447918679405 (to 8 pm eve or Saturday AMs) or send me an email with a CV to matt.greig@advregulatory.com ______________________________________________________________________________________________ About Advanced Advanced Regulatory is a division of Advanced Search and Selection Ltd and has been operating since 2004. We are registered and licensed to recruit through the United Kingdom, mainland Europe and the Americas. Keywords / Key words: ICH GCP, QA PhV, GPhP, Quality Jobs, Jobs in QA, Audit Manager, Audit Senior Manager, Audit Director, PhV QA, Jobs in PhV QA, Jobs in Quality Assurance, Jobs in GCP Compliance.

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