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Regulatory Affairs Manager, Biotech, Switzerland, perm, officebased

This job is no longer available

Employer
Meet Recruitment
Posted
Wednesday, September 05, 2012
Closes
Wednesday, October 03, 2012
Ref
5912
Location
Zurich, Lucerne, Zug area
Contract Type
Permanent
Hours
Salary
from CHF140,000, no limit, based on experience

Further information

 Regulatory Affairs Manager
Senior Regulatory Affairs Manager
Associate Director Regulatory Affairs
Director Regulatory Affairs
Senior Director Regulatory Affairs

NB: You must be eligible to live and work in Switzerland.

 

Client

This is a growing Biotech company with offices around the world and an exciting pipeline of projects - more details on application

Duties
•Prepare regulatory documents and applications according to EU standards
•Maintain the regulatory affairs database ensuring high quality data delivered in timely fashion
•Represent the company at client meetings
•Manage the team of associates (line management)

Skills
•Circa 5 years experience in pharmaceutical setting, minimum 3 years in Regulatory role
•Ability to autonomously plan and execute multiple tasks
•Project management skills
•Fluent verbal and written English - able to communicate and present
 


Salary

from CHF 140,000 + bonuses and benefits, no upper limit

Associated Keywords

Pharmaceutical, Biotech, Biotechnology, Biochemistry, CRO, Pharma, Pharmaceutical, Clinical, Clinical Regulatory Affairs, Regulatory Affairs Manager, Clinical Regulatory Affairs Director, Senior Regulatory Affairs Manager, Switzerland, Europe, Regulatory Affairs Manager, Regulatory Affairs Director, Regulatory Affairs Leader, Regulatory Affairs Line Manager, Global Regulatory Affairs Management, Switzerland, Arth, Cham, Ebikon, Knonau, Hausen am Albis, Baar, Unterageri, Gersau, Ingenbhol, Schwyz, Emmen, Inwil, Sins, Horgen, Einsiedein, Adliswil, Zurich, Uster, Ruti, Volketswil, District 11, Wohlen, Ruswil, Willisau, Reiden, Zofingen, Langenthal, Olten, Aarau, Baden, Bulach, Winterthur, Wattwil, Glarus, Schwanden, Altdorf, Andermatt, Stans, Lucerne, Samen, Giswil, Lungern, Linthal, Elm, Schaffhausen, Frauenfeld, Wil, Walenstadt, Liechtenstein, Vaduz, Flums, Sargans


Apply NOW

Full company details and job description are available upon application; no CV is submitted until full discussion has taken place. Please contact Craig Edwards at Meet on +44 203 178 7488 or email craig@peoplewithchemistry.com

Contact via LinkedIn: http://uk.linkedin.com/in/craigedwardsmeet

Follow me on Twitter:

@meet_craig

Meet are good people who are great at recruitment. We're proud to partner with the industry's leading Pharmaceutical and Healthcare companies, helping them find and secure the best global talent available

Find out more about Meet at www.peoplewithchemistry.com

I currently recruit within the Pharmaceutical/Biotech/Clinical Research/Medical Device industries, specialising within the field of Regulatory Affairs, on a Contract, Permanent and Retained basis throughout Europe

We cater for all levels of candidates including:

Regulatory Executive/Associate/Officer/Specialist
Regulatory Consultant/Contractor
Senior Regulatory Affairs Executive/Officer/Associate
Regulatory Affairs Manager
Senior Regulatory Affairs Manager
Associate Director Regulatory Affairs
Director Regulatory Affairs
Senior Director Regulatory Affairs
Vice President Regulatory Affairs

Specialties: Regulatory Affairs, Regulatory Operations Submissions Specialists Post Approval Post Marketing Clinical Regulatory eCTD CMC Compliance, Pharmaceutical, Pharma, Biopharma, Biotechnology, CRO, Medical Device, EU, CEE, UK, IMB, FDA.
 

Meet Recruitment


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