- Global Director Regulatory Affairs / Quality Assurance: Devices
Looking for a Global Leading Regulatory/Quality Position? Click Here...
- Regulatory Affairs and Quality Assurance Medical Devices Manager-permanent-London-£70.000
Due to it's global presence, the company is continuously growing and taking on new, very challenging projects. If you are interested in being part of a dynamic team, and work in a busy environment, then don't hesitate to apply for this position.
- Quality and Regulatory Affairs Specialist
Quality and Regulatory Specialist - Contract
Medical devices - negotiable hourly rate
- Head of Quality Assurance & Regulatory Affairs
Exciting opportunity for Head of Quality Assurance and Regulatory Affairs with expanding diagnostics company!
- Quality Assurance & Regulatory Affairs
An experienced quality/regulatory professional is required for an exciting and fast growing company based in Surrey.This role will be office based and some travel may be required to carry out supplier audits, to meet with regulatory bodies, and attend relevant meetings.
- Regulatory Affairs Specialist
ProClinical are recruiting on behalf of a leading contract research organisation who have a vacancy for a Regulatory Affairs Specialist. In this job, you will be working at a company that is at the forefront of drug development and has helped to commercialise many leading therapies. This role can be based in Hertfordshire/ Buckinghamshire. This is a 3 month contract role with the possibility of an extension. ...
- Regulatory Affairs Specialist
An exciting job vacancy has emerged for a Regulatory Affairs Specialist at one of the world's largest global CROs. This contract research organisation provides support services to many of the biggest names in pharmaceuticals, biotech, medical devices and health care, and has helped to commercialise many leading therapies. This position will be based at their UK site in in Hertfordshire/ Buckinghamshire. This is a 3 month contract role with the possibility of an extension. ...
- Senior Regulatory Associate
Novella focuses on providing excellent training and career development opportunities, encouraging growth from within our talented work force. Novella specialises in leveraging technology and Clinical Research and continues to improve the quality and service across a broad range of therapeutic areas including Oncology and Medical Devices. Our parent company is one of the World’s leading not profit research organisations, and you will be joining a passionate and motivated team.
- Senior Regulatory Affairs Manager (m/w)
Senior Regulatory Affairs Consultant (m/f)Office-based Munich AreaRole / Description:- Provide expert advice and support to global clients in the pharmaceutical industry- Strong involvement in Business Development activities, including attending client meetings and supporting the Head of Business Development in client acquisition activities- Responsible for project management team- Managing successful initiation, execution and completion of Regulatory and CMC projects- Main point of contact ...
- Manager Regulatory Affairs (M/F) - CMC
A fantastic new position has become available within a leading pharmaceutical company for Manager Regulatory Affairs.
My client is a thriving, cutting edge company specialising in providing high quality solutions for truly international studies.