Regulatory Affairs Manager
£negotiable |
Berkshire |
Regulatory Affairs, Pharmaceutical Company/Sponsor side | Permanent
| Ref:888625
A global pharma who work within a specialist therapy area are currently recruiting 2x Regulatory Affairs Managers to focus on Northern European and Middle Eastern regions. They boast offices across the globe and are committed to ensuring patients have access to quality treatments.
Global specialist pharma company
Offices worldwide
Specialist therapy area
Proven success with their core products
As the Regulatory Affairs Manager (EU or Emerging Markets) you will be responsible for;
Managing and maintaining a portfolio of dossiers / technical files across all products, ensuring they remain compliant with relevant legislation
Creating new technical files / dossiers for new products in new markets
Focusing on either Northern Europe OR Emerging Markets (Middle East)
Renewals/variations
Full lifecycle management
You will have the following experience:
Full lifecycle Regulatory Affairs experience within pharma (ideally 5 years )
Experienced in either EU/UK regulatory affairs or emerging markets (Middle Eastern regions)
Good project management skills
Good stakeholder management skills
This Regulatory Affairs Manager (EU or Emerging Markets) job is a great role and won't be around for long! So don't delay. If you are unsure and need some advice, give me a ring, otherwise just click apply, upload your CV and send, it's really that easy!
Unless otherwise stated, if applying for a job within the European Union, you must ensure that you are already authorised to work there. Carrot Pharma Recruitment Ltd acts as an Employment Business and an Employment Agency on behalf of our client in recruitment for this role.
Which team and area do you work/specialise in?
I work in the Regulatory Affairs team and recruit for Regulatory Affairs professionals at all levels within Pharma, Medical Devices companies and Regulatory Consultancies
What are some of the typical roles you cover?
I cover Regulatory Affairs positions at all levels within Pharma, Medical Devices and Regulatory Consultancies, these typically include;
Regulatory Affairs Associate jobs, Regulatory Affairs Executive jobs, Regulatory Affairs Senior Associate jobs, Regulatory Affairs Manager jobs, Regulatory Affairs Senior Manager jobs, Regulatory Affairs Director jobs, Regulatory Affairs Consultant jobs, Regulatory Writer jobs and Medical Writer jobs.
What are the hot issues in your sector currently?
Within Medical Devices it is the transition from MDD to MDR in May 2020. A lot of medical device companies are hiring Regulatory professionals to prepare their company for the transition
What’s makes you #DistinctlyDifferent?
I take pride in getting to know my candidates on a personal level as well as professional. Changing jobs is a big decision for most people so I like to ensure I am placing my candidates in a role that not only matches their career aspirations but also suits their personal situation and key motivations.
