A leading pharmaceutical company based in the South require a Senior Regulatory Affairs Executive to undertake a 6 month contract position, with the opportunity to extend for the right candidate. The company are a major brand with an extensive portfolio of therapeutic products at all stages of the life cycle. This is an exciting opportunity to join a leading brand in a period of major growth.
Regulatory Affairs Executive\Regulatory Affairs Project Manager
Fixed-Term Contract (7 months)
A top pan-European specialist pharmaceutical company is actively looking for motivated and pragmatic individuals that approach their work with vigour to join their internationally acclaimed company as a Regulatory Affairs Executive/Regulatory Affairs Project Manager.
Responsibilities will include; Review SPCs, artwork and PILs, prepare submissions including CMC variations, SPC, labelling and renewals and ensure documentation and submissions are on time and liaise with the authorities.
For further information about this role or to arrange a confidential conversation about other vacancies within regulatory affairs please contact Tim Barratt on +44 (0)1727 817 626 or send you CV to firstname.lastname@example.org
Opportunity to join this successful Global Biopharmaceutical Company as a Principal Regulatory Affairs Executive. You will be responsible for preparing high quality Module 3/CMC documentation for all regulatory submissions; liaising with relevant departments to ensure regulatory requirements for these submissions are met. 6 month contract.
Lead projects for the Preparation and submission of marketing authorisation applications and Variations Type I & II & gain full project lifecyle experince - To apply for this position please call Advanced Regulatory on 0207 801 3380 and ask for Theo Moore or Mark Twigdon email your Cv to email@example.com in the strictest confidence to receive full details on a number of positions available within regulatory affairs.
*** Be the CMC Regulatory lead and provide in-depth working knowledge of CMC and regulatory procedures, legislation and guidelines for submissions applicable to biotechnology and products across EU and Emerging Markets *** Call Marc Van de Voorde or Theo Moore on +41- (0)41 710 51 00 or on +44 (0)207 801 3384 or email us at firstname.lastname@example.org
Regulatory Affairs Manager, CMC â€“ Switzerland - Provide CMC dossiers for MAA submissions in the EU and Emerging Markets
Call Marc Van de Voorde on +41(0)41-710.51.00 or 0207 801 3385 or email email@example.com.
***The role will require you to lead regional CMC strategies through to fulfilment, optimising timelines where possible by working well with cross functional departments and your colleagues in Global Regulatory and Global RA CMC***
Call Theo Moore on +44 (0)207 801 3384 or email me in confidence at firstname.lastname@example.org
Join an expanding European regulatory affairs department in a company with a very strong portfolio of new and marketed products. This role will encourage you to build and develop your existing Project management skills and experience. Location Maidenhead - Salary to ÂŁ34K -
Reply in confidence to Theo Moore or Mark Twigdon today on +44 (0)207 801 3380 or send your CV to CV@AdvRegulatory.com
This is an exciting opportunity to join the regulatory affairs team within a top Global Pharma. The role is a 9 month contract, with the potential to extend for the right candidate. You will report to the Regulatory Director, and will be expected to liaise with other teams. The company are a major brand with an extensive portfolio of therapeutics at all stages of the life cycle. For a committed and driven individual this is an excellent opportunity working for a globally respected company.
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