- 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 / Publisher
An excellent opportunity has arisen for an experienced Regulatory Publisher to join a fast growing team based in Berkshire, UK. The ideal candidate will have a strong background in publishing regulatory submissions (MAAs, INDs, CTAs etc) and enjoy working within a dynamic and fast paced environment. If you have team leadership skills and enjoy working within a consulting environment with Global Fortune 500 clients, this role is for you!
- Senior CMC Consultant
Senior Regulatory Affairs Consultant CMC – Permanent – Cambridge
My 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. ...
- GMP Auditor (Analytical Lab Expert)
The primary purpose of this job is to perform and manage GMP compliance audits of GMS sites supplying highly regulated markets. The Audit Manager will also perform assessment and support for regulatory inspection preparation for GMS sites supplying highly regulated markets. In addition for cause audits at specific GMS sites may be performed as needed.
This job can be based at any of the Company sites throughout Europe.
- Affiliate Drug Regulatory Associate
This position will be responsible for execution and management of regional life-cycle submissions for all of our clients’ products as well as new product registrations by focusing on local needs of Affiliate Drug Regulatory Affairs (DRA) teams to ensure right first-time submissions to Health Authorities.
- Senior Regulatory Affairs Specialist
Senior Regulatory Affairs Specialist required for post marketing role - a permanent position with a global pharma company. Competitive salary offered.
- Regulatory Operations - Submissions Associate Manager
My client, a Global Management consultancy is searching for a Regulatory Operations - Submissions Associate Manager to join their team.
This role is permanent and is based in Berkshire offering a very competitive salary plus benefits if you are successful.
For more information on this exciting role, please contact Richard Williamson on 0203 327 3072 or apply via this advert.
- Therapeutic Area Programming Director – Biometrics & Information Sciences
We are looking for an exceptional Therapeutic Area (TA) Programming Director to join our world-class Biometrics community at AstraZeneca.
- Regulatory Affairs Manager (w/m) (UK – office based)
Shared Work – Shared Vision: The way we do business, a promised standard that includes ongoing support from a specialized team dedicated to meeting or exceeding our clients expectations.
Are you looking for a new challenge in a global and fast moving company? Then SynteractHCR offers you a dynamic environment, the opportunity to bring your experience in and leave a footprint in the Global Regulatory Affairs Team.