- Senior Regulatory Affairs Specialist-Expert in FDA submissions
A fantastic role within regulatory affairs has come in with the opportunity to work on the exciting American market. Our client are looking for a senior regulatory affairs specialist to join their global team to work on exciting international projects. Our client are a world leader within medical devices, allowing you to progress your career with a reputable company.
- Senior Regulatory Submissions Specialist
My client, a rapidly growing Biopharmaceutical organisation is now looking to extend their Regulatory Submission team on a global basis. This position will play an integral part in the successful management and implementation for their global submissions efforts within publishing. Due to the needs for this position, they now require a talented and dedicated individual to join the team in a Senior Specialist function.
- Regulatory Affairs Manager \ Project Manager \ Regulatory Submissions Lead
Regulatory Affairs Manager \ Project Manager \ Regulatory Submissions Lead
£50,000 - £65,000 – flexibility for highly experienced candidates
Location: Flexible home working (can be entirely home based) or East Anglia
Are you looking for a flexible company which allows you to be based from home?
Are you interested in working for a forward thinking, innovative company?
- Regulatory Affairs Manager \ Regulatory Affairs Project Manager \ Regulatory Submissions
Regulatory Affairs Manager \ Regulatory Affairs Project Manager \ Regulatory Submissions
Our client is a leading global contract research organisation providing drug discovery, development and lifecycle management services. Their clients and partners include pharmaceutical, biotechnology, medical device, academic and government organisations.
- Regulatory Submissions Manager
Regulatory Submissions Manager - Biopharmaceutical group
- Regulatory Submissions Manager
Keywords:Regulatory Operations, Regulatory Publishing, NeES, eCTD, DocumentumGlobal Regulatory Operations, GRO, manager
- Regulatory Affairs Manager CMC
Manager, Regulatory Affairs CMC – Emerging MarketsThe CompanyMy 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. ...
- Senior CMC Consultant
Senior Regulatory Affairs Consultant CMC – Permanent – CambridgeMy client, a leading Regulatory Affairs consultancy, is looking for an experienced candidate to join them and aid their CMC Biologics side. My client works with over 400 global pharmaceutical and biotechnology customers and they need an expert with CMC (ATMP) to help advise these key industry giants. ...
- Analytical Expert (m/f) Inhalation Job
You can join a top international pharmaceutical company in their R&D facility in Germany. You will lead and manage as Analytical Expert technical development activities for the development of inhalation products (MDI and DPI) for assigned projects and ensure that they are conducted timely and with required quality considering Quality by Design principles. ...
- Principal Programmer
Ian Marlow at CK Clinical is recruiting for Principal Programmer for a pharmaceutical company in Cambridgeshire. Description: • Drives good design to generate the data...