Regulatory Affairs & Quality Manager, Europe
A global in vitro diagnostics company, based in Germany- Frankfurt, specialized in immunohematology and corresponding automation systems is currently looking for a Regulatory Affairs & Quality Manager, Europe
Regulatory Affairs & Quality Manager
Sicherstellung der Kommunikation innerhalb des Konzerns und entsprechend der nationalen und europĂ¤ischen Vorgaben
Leitung des lokalen QualitĂ¤ts- und Beschwerdemanagements
Implementierung und Optimierung regulatorischer und qualitĂ¤tsrelevanter MaĂźnahmen und Prozesse
My client is a niche provider of innovative Medical Devices that are used throughout the world with ground-breaking results for thousands of patients. Due to the nature of their devices, it is increasingly important for my client to recruit the very best candidates within the industry and they are now looking to expand their Regulatory & Quality team with their newest addition.
This position is ideal for those looking for a role which will focus on CMC but still allow you to work through the full project lifecycle for both Pharma and Biotech projects. If you have 1-3 years RA experience with a focus on CMC and want to gain expansive project management experience then this is going to be the role for you. Contact Theo Moore on 0207 801 3384.
My innovative and expanding medium sized Pharmaceutical client is seeking a regulatory affairs snr manager with broad experience for a regulatory affairs role covering both pre and post marketing phases for a range of therapeutic categories and dosage forms. Contact Theo Moore for full details or to apply on 0207 801 3384 or via email at Cv@advregulatory.com
This role will give you full hands on Centralised procedure submissions experience then allow you to move into a global role. This really is an excellent opportunity to develop your expertise in a friendly & commercially focused environment for one of the worlds fastest growing Pharma companies.
An expanding and highly successful Bio-Pharmaceutical company with an extensive pipeline and a high value commercial portfolio is seeking a dynamic, innovative and highly motivated character to take the lead for International Regulatory strategies and submissions. Excellent salary; fullâ€“relocation package; excellent career prospects. Contact Theo Moore on +44 (0)207 801 3384 or apply via Theo@advregulatory.com
My leading Biopharmaceutical client is looking for an experience and motivated CMC bio senior manager to take the lead on a number of projects. You will be working with an excellent pipeline in a strong team, where the focus is on high level strategic input Contact Theo Moore +44 (0) 207 801 3384 or email on firstname.lastname@example.org
Take responsibility for new product registration, maintenance of existing product licences and
compliance of promotion activities under the supervision of the Registration Manager. Interact
with EC Registration, Clinical Managers, Marketing Managers and Global Regulatory Affairs,
on day-to-day regulatory issues. Contact Theo Moore or Matt Greig on +44 208 801
This role will give you the opportunity to cover stages of development and take the lead for an EU MAA via the centralized procedure in a leadership role where you will be involved in both developing and delivering EU and sometimes global regulatory strategies. Contact Theo Moore on +44 207 801 3380 or email your cv in confidence to Cv@advregulatory.com
PharmiWeb.com is Europe's leading industry-sponsored portal for the Pharmaceutical sector, providing the latest jobs, news, features and events listings.
The information provided on PharmiWeb.com is designed to support, not replace, the relationship that exists between a patient/site visitor and his/her