- Director Regulatory Affairs, EU - UK Based
Pharm-Olam International are looking for an established regulatory professional from a CRO background who is experienced in directing and submitting EU submissions. Ideally this position will be UK office based, however Pharm-Olam will consider other european office based locations.
- PW 6283 Director/Senior Director Regulatory Affairs
This is a key opportunity for an experienced regulatory professional to play a Deputy Head role with broad responsibility for the Neuro and General Medicines therapy area of this global Pharma company. You will hold budgetary responsibility, attend key EU Health Authority meetings, play the EU regulatory lead for key General Medicines development projects and closely monitor the regulatory environment.
- Regulatory Affairs Associate Director / EU & Global Strategy and Project Management - Belgium
My client has exciting products and challenging project work. It’s a company with a very good growth rate and has a promising future. They have lots of products in the pipeline which means more growth and exciting times are ahead. If you wish to apply for this role send your CV to email@example.com or call Theo Moore or Matt Grieg in the UK London office, on +44 (0)207 801 3380
- Regulatory Affairs Associate Director - Netherlands - EU & International strategic leadership role - Excellent Portfolio - Expanding Pharma Company
This will be a results orientated strategic leadership role where your strategy and regulatory knowledge will carve a path for product submissions and registrations ion the EU and other major RoW/International territories.If you wish to apply for this role send your CV to firstname.lastname@example.org or call Theo Moore on Matt Grieg on +44 (0)207 801 3380
- Regulatory Affairs Associate Director – Brussels - Take the lead for Centralised filings and EU/ROW strategy – Salary to 120,000 + Car + Bonus
As a high performing organisation, my client is committed to growing and developing their people and within this International multi-cultural regulatory department you will find challenges and opportunities to keep you interested, motivated and developing for many years to come.If you wish to apply for this role send your CV to email@example.com or call Theo Moore or Matt Greig in the UK London office, on +44 (0)207 801 3380
- Director Regulatory Affairs - Paris
Pharm-Olam International are looking to expand their European Regulatory department with the opening of Director, Regulatory Affairs to be located in Paris. The ideal candidate will have MAA experience and have experience compiling filings for EU countries as well as non-EU submissions and be up to date with all the latest EMA and international regulations, guidelines, and regulatory trends. Previous line management experience is desirable but not essential.
- Senior Director, Regulatory Affairs - Hertfordshire
As Senior Director, Regulatory Affairs the incumbent will be the Deputy Head for the Neuroscience & General Medicines (NGM) Therapeutic Area (TA). Duties to include: 1. Manage the EU NGM TA budget. 2. Attend EU Health Authority meetings as NGM TA representative. 3. Monitor the EU regulatory environment & assess implications for NGM products 4. Advice NGM TA Heads on emerging regulatory trends in EU
- Associate Director, Regulatory Affairs
Overview:Skills Alliance are currently working on an exclusive project with an emerging biopharmaceutical organisation who are looking to recruit an Associate Director, Regulatory Affairs. This...
- Deputy Head of Regulatory Affairs - Neuroscience and GM
Senior Director, Regulatory AffairsAn extremely successful midsize pharma company based on the outskirts of North London are looking to recruit a Senior Director Regulatory Affairs to be the Deputy Head for their Neuroscience and General medicine department to join on a permanent basis. ...
- Regulatory Affairs Manager for EU and global Projects – CMC focused role – develop your expertise in Mabs, Vaccines and ATMPs - Lausanne
This role with develop your CMC biotech experience to the highest level as you work with EU and Global clients on strategies and submissions, whilst learning from some of the industry’s most experienced CMC Biotech regulatory technicians. If you wish to apply for this role send your CV to firstname.lastname@example.org or call Theo Moore or Matt Grieg in the London office on +44 (0)207 801 3380 -