Regulatory affairs
At ACHIEVA we welcome candidates from all areas of Regulatory Affairs.
Perhaps you’re a specialist in Drug Development, In-vitro Diagnostics, Medical Devices or Biotechnology. In a complex global market of constant change, your skills are critical to developing safe and effective innovations.
Within Regulatory Affairs we connect ambitious candidates to prestigious roles spanning everything from product development, Clinical Trial Applications and Marketing Authorisation Applications, to tracking and acting on evolving legislation, bringing products to market, and negotiating licence variations and renewals.
Among the roles ACHIEVA fills for our clients are:
- Regulatory Affairs Associate / Officer
- Regulatory Affairs Senior Associate / Officer
- Regulatory Affairs Manager / Senior Manager
- Regulatory Affairs Director / Senior Director
- Head of Regulatory Affairs
- Vice President Regulatory Affairs
- Freelance Regulatory Affairs Consultant
- Regulatory Writer / Medical Writer
To register with ACHIEVA submit your CV by clicking the ‘REGISTER WITH ACHIEVA’ button. Alternatively email us at recruitment@achieva.co.uk or call us on +44 (0) 1727 811634 and our specialist staff will be more than happy to assist.
Latest Pharma News
The core skills required to succeed in the world of pharmaceuticals
Working in pharmaceuticals gives people the opportunity to make a real difference by pushing boundaries,…
Pharamceuticals – The industry with the key to our freedom
Earlier this month, Mike Hennessey Sr, Chairman and Founder of the USA’s biggest medical media…
NEW YEAR, NEW BRAND – INTRODUCING ACHIEVA
2021 has been hailed by many as a year of new beginnings and for our…