They are looking for an individual that is hard working and self motivated to assist with all things regulatory.
A London based Start-up Medical Device company developing a Class 1 Measuring Device is on the look out for a Regulatory Affairs Manager to support their growing business.
Responsibilities will include: Oversee the development and management of technical files, dossiers, and regulatory documents for medical devices and pharmaceuticals.
Posted by Park Street People • £23/hr to £23.70/hr
Our client, a global pharmaceutical company, is currently looking for a Senior Regulatory Affairs Associate to join their team in Cambridge or West London (Uxbridge).
Roles are typically remote-by-design but candidates do need to be prepared to travel to their nearest office on occasions for key meetings.
This is a great opportunity to work for a pharmaceutical company who have created a centre of excellence and constantly focus on driving innovation and using cutting edge techniques in their science.
Posted by Hays Specialist Recruitment Limited • £25/hr to £32/hr
Senior Regulatory Affairs Associate EUYour new company
This well-known biopharmaceutical company is looking for an experienced Senior Regulatory Affairs Associate EU to join the team on a contracting basis.
This is a 12-month contract job with scope for extension.Your new role
Posted by Hays Specialist Recruitment Limited • £50/hr to £70/hr
This is an exciting Regulatory Affairs contracting position which will be reporting to the Regulatory Lead and will have you leading regulatory submission strategies, globally.
You will be working as the Senior Regulatory Affairs Manager (EU and US markets) and be reporting directly to the Regulatory Portfolio Lead.
Alongside their already large portfolio of products both established and in development, they have successfully brought on a new product within the neurology space.
Posted by ProTech Recruitment Ltd • £75K/yr to £95K/yr
A fast growing healthcare technology company is looking for a highly skilled and motivated Head of Quality and Regulatory Affairs to join their team.
This individual will play a critical role in guiding the organisation's innovative medical products through the regulatory approval process, ensuring compliance with global quality standards.
This is an exciting opportunity for someone who is passionate about navigating complex regulatory landscapes to bring cutting-edge technologies to market.
Posted by Nursing and Midwifery Council • £61K/yr to £67K/yr
About the role
You will support effective engagement with the Professional Standards Authority (PSA) and will support the PSA & Review Groups Strategic Lead by liaising with internal stakeholders and senior leaders to ensure timely responses to PSA correspondence.
This includes preparing for the PSA annual performance and detailed periodic reviews of our performance against the 18 Standards of Good Regulation.