Q-Med söker Group Manager, Regulatory Affairs. Job in Uppsala, Uppsala Sweden
Q-Med söker Group Manager, Regulatory Affairs.
The Regulatory Affairs Department at Q-Med is responsible for all Regulatory aspects of our business including new product registrations, line extensions, Life Cycle Management of the portfolio of licences, change control submissions and CMC writing. We are now looking for a Group Manager to take responsibility for the team working on the family of products encompassing all regulatory aspects of the portfolio.
We are looking for a person with several years experience of Regulatory Affairs preferably from a manufacturing and compliance perspective. You should also have several years’ management experience and be able to work with change and challenges as part of your every day tasks.
You are flexible and used to taking responsibility. Fluency in English both verbal and written is a must.
Your responsibilities will include:
· Development of working methods and routines for the team
· Driving the team forward in order to reach the overall objectives set for the organization.
· Ensure that the team has the necessary resource and competencies in order to succeed
· Staff and budget responsibility
Who are you?
You have a degree at University level within the Pharmaceuticalor similar areas. You have experience from similar roles in the Medical Device or Pharmaceutical industry. We require several years management responsibility and that you are active, involved, flexible and focused. The ability to communicate well both internally within the organization and externally with colleagues, authorities and affiliates is a must.
We can offer you a role in a very exciting work environmanet with many international contacts.
For further information please contact:
Sinéad Breen, Head of Regulatory Affairs, 0768-981230
We want your application as soon as possible.
You may apply through www.q-med.com
Welcome with your application!
Sökord: Regulatory Affairs, gruppchef, chef, registrering
