This site uses cookies. By continuing to browse the site you are agreeing to our use of cookies. Find out more here.

Close Message for pharmaceutical industry jobs
NonStop Recruitment is dedicated to putting job seekers looking for pharmaceutical industry jobs in touch with recruiters and employers.

Similar jobs you may be interested in:

Regulatory and Quality Officer - Big Medical Device Portfolio
Chef de projet Affaires Réglementaires enregistrement au Global
Chargé(e) Affaires Réglementaire - Lifecycle Management
Apotheker gezocht: carrière in de industrie!
Regulatory Affairs Medical Devices: boost your career!

To receive a FREE weekly email alert of all the latest pharmaceutical industry jobs added to our database enter your email address below.

Submit | Tell me more...

Sister sites:
Our sister site Our sister site
Partner sites:

At Burntsky Limited we work with a number of third parties in order to maximise the reach of the jobs posted with us including but not limited to:

JooblePartner Jooble
UK Jobs
Science Jobs

Job Details
This job has expired. Click here to view similar jobs.
Contact Details:
Oana Stan
NonStop Consulting
+44 (0)207 940 2105

NonStop Consulting
25 Canada Square
Canary Wharf
E14 5LQ
United Kingdom

Regulatory Affairs CMC (Associate) Manager-TOP PHARMA-ASAP

Business Type: Pharmaceutical Company
Job Type: Regulatory Affairs
Job Level: Experienced (non manager)
Position: Contract
Location: Switzerland
Reference: NV2
Closing Date: 09/09/19
Job Details:

Who says that you can''t have it all? Great position? Fantastic company? Applying now is the first step to success!

You will be working for one of the biggest names in Pharma, where you will be able to grow your network and gain exposure for future work. Imagine not thinking what you are going to do next, because the opportunities always come to you.

We are looking for:

  • Regulatory experience preferred, and/or experience in drug/biopharmaceuticals
  • Working knowledge of chemistry/biotechnology, analytics or pharmaceutical technology. Knowledge of the drug development process desirable. Ability to critically evaluate data from a broad range of scientific disciplines.
  • Knowledge/experience of regulations, guidelines for NCEs and product life cycle maintenance desirable.

Posted: 12/08/2019 | NPJ Ref: 240168
line graphic

Compatible with:

JobMate   Broadbean   Idibu

Site optimised for Internet Explorer 8+ / Firefox 3+
View a complete Jobs Listing

Credit cards image