- Regulatory Affairs Opportunities in the UK - Global CRO - UK
Regulatory Affairs Opportunities in the UK - Global CRO - UK - Multiple Levels If you would like to apply for the position or wish to learn more about the role and company please call Mark on 0044 (0) 207 255 6665 or email your CV with a brief covering note to firstname.lastname@example.org
- Reg Affairs Consultant - Medical Devices - Perm
If you woke up this morning wishing you could work with an expansive portfolio of class I to III devices on a variety of engaging projects, look no further!My client are a consultancy that are looking for experienced regulatory affairs professionals to come on board as soon as possible to take part in a variety of projects within the medical devices area. ...
- Senior Regulatory Affairs Manager (EU lifecycle)
Full-time opportunity for a Senior Regulatory Manager to join exciting pharma company within an EU role!!!
- PW 6354 Regulatory Affairs Systems Associate Director
Opportunity for a senior regulatory systems professional, to join this exciting pharma organisation as Regulatory Information Management (RIM) Associate Director. Responsible for managing global strategy, implementation and maintenance of regulatory systems and processes. The role requires you to lead the RIM team to effectively deliver the operational plan.
- PW 6353 Associate Director Regulatory Affairs (Lifecycle)
Opportunity for a senior regulatory professional to join this exciting pharma organisation heading up their international lifecycle team. Responsible for managing the team, global regulatory strategy, maintain existing product licenses and integrate newly approved products into the team. In return you will be highly rewarded in this role both financially and career progression.
- Senior Regulatory Affairs Manager
Regulatory Affairs Senior Manager – 12 month contract – West London/MiddlesexAn exciting opportunity has come up for a Regulatory Affairs Manager to be based in the West London/Middlesex area. Responsible for supporting regulatory aspects of a product’s development, primarily in relation to Marketing Authorisation Applications but also, if necessary, supporting Clinical Trial Applications. ...
- Regulatory Affairs Manager - MAA
Regulatory Affairs Manager – 12 month contract – West London/MiddlesexAn exciting opportunity has come up for a Regulatory Affairs Manager to be based in the West London/Middlesex area. Responsible for supporting regulatory aspects of a product’s development, primarily in relation to Marketing Authorisation Applications but also, if necessary, supporting Clinical Trial Applications. ...
- PW 6335 Global Submission Specialist / Regulatory Submissions Project Manager
Opportunity for a Submissions Manager to join this Top 20 Pharma on a fixed term contract as our Client’s Global Regulatory Submissions Specialist. The role is office based in the South East, focuses on compliant submissions, Ectd standardisation and sits within a cross functional global team. Contract length is 6 months and strong likelihood to extend further.
- Senior Regulatory & Medical Affairs Executive - Hertfordshire
Senior Regulatory Affairs professional needed to be the 2nd in command within the Medical Affairs and Regulatory department of a mid sized Biopharmaceutical company in Hertfordshire. This intrinsically broad post registration role has an extremely wide remit including, Maintaining licences, Marketing Authorisations, Pharmacovigilance, Promotional material & the use of the ZINC System
- Regulatory Affairs Officer\Regulatory Affairs Associate
Regulatory Affairs Officer\Regulatory Affairs Associate
•Do you want to work for an international Pharma Company?
•Do you want to work for a company with cutting edge innovative Products?