- Regulatory Affairs Manager CMC
Manager, Regulatory Affairs CMC – Emerging Markets
My client, a leading Biotech company, with a global presence and highly reputable market presence, is looking for a Manager within their Regulatory Team. This company is rapidly growing year on year and producing products that are changing the world. With more and more MA applications happening each year, their expansion is set to continue exponentially. ...
- Regulatory Submission Specialist (m/f) - Ref. 895600
Expert in Clinical Submissions, 6 months project with an option to prolong, office based as sponsor in Brussels
- Regulatory Specialist-Growing market of Molecular Diagnostics
Regulatory Specialist-Growing market of Molecular Diagnostics
Working as a Regulatory Affairs expert for a company who focus on Molecular Diagnostics you will be exposed to a wide array of global regulations for IVD submissions. With the company rapidly expanding they are seeking somebody with a good platform of hands on global submissions experience whilst offering training and guidance on future tasks, making this an ideal role for professional growth.
- Associate Director Regulatory Affairs
Associate Director, Regulatory Affairs - Cambridgeshire
A lot of regulatory professionals will be lucky if they get within touching distance of a MAA in a 4/5 year period. My client is expecting to push 1 or 2 out a year. Be part of something big and help it become even bigger!
My client, a leading Biotech company with global coverage and highly reputable market presence, is looking for a Manager within their Pharmacovigilance team. ...
- Regulatory Program Manager - Oncology
Want to work with the best in Europe? Want a new and stimulating opportunity? I want to talk to you!
Join a team with company with a Global presence in a rapidly growing industry, who have an exceptional reputation in the industry for providing excellent opportunity to grow and develop.
- *** Regulatory Affairs Senior Manager CMC Biologics *** Brussels *** Provide Strategic leadership for CMC bio projects *** European Market***
My leading Biopharmaceutical client is looking for an experience and motivated CMC bio senior manager to take the lead on a number of projects. You will be working with an excellent pipeline in a strong team, where the focus is on high level strategic input. Call Theo Moore or Matt Grieg in the London office on +44 (0)207 801 3380 - or Andrew Barnes in our Swiss office, on +41 41 710 5100
- ***Regulatory Affairs Senior Manager CMC *** Basel, Switzerland *** Provide Strategic leadership for CMC bio projects *** Excellent pipeline ***
***Regulatory Affairs Senior Manager CMC Biologics *** Basel, Switzerland *** Provide Strategic leadership for CMC bio projects *** Excellent pipeline *** Contact Andrew Barnes in our Swiss Office on +41 41 710 51 00 or Theo Moore on or +44 (0) 207 801 3384
- DOCUMENT AND DATA MANAGEMENT EXPERT (100% OUTSOURCED TO SPONSOR) - Amsterdam, Netherlands
An outstanding opportunity to join one of the world’s leading contract research organisations and be part of a dynamic and growing international company. Join PRA Health Sciences as a Document and Data Management Expert and help realize your career potential.
- Regulatory Affairs Manager CTA – West London
Regulatory Affairs Manager CTA - West London
My client, a dynamic company which is globally recognised as an extremely reputable company has an urgent opening for a Regulatory Affairs Manager CTA. The successful candidate will join the EU Regulatory Team based in the UK.
- Senior Regulatory Affairs Consultant
Senior Regulatory Affairs Consultant –Regulatory – Home based
This company is a top 5 global CRO with a large and ever growing consulting arm. This company is global company with over 10,000 employees across all continents. They are a company that help their clients get medicines into the hands of those who need them most. They offer scientific know how, industry expertise and an outstanding environment to learn and grow. ...