Cpl Life Sciences is collaborating with a prestigious global drug development consultancy business that specialises in supporting pharma, biotechs, spin-outs, and academic groups with drug development activities.
The business has a specific focus on advanced therapies, cell therapy, ATMPS, and other niche and challenging therapeutic areas.
An opportunity to join a growing business that supports pharmaceuticals, biotechs, spin-outs and academic groups to translate science into medicinal products.
An exciting opportunity for a German Speaking candidate with a background in Regulatory Affairs to join this highly successful business that provide labelling, consumer information and regulatory advice.
OPPORTUNITY HIGHLIGHTS
Fully remote role.
This role is for a fluent German Speaking candidate only.
Posted by DivalentineCalver Recruitment Ltd • £50K/yr to £70K/yr
This role oversees Regulatory strategy for the organisation, providing leadership and guidance to the business on Regulatory matters for Food, Feed and Personal care activity in the UK and other markets to drive compliance within their ingredient agent, brokerage and solution manufacturing businesses.
Our client is a well respected and world class distributor of functional ingredients and is seeking an experienced Regulatory Affairs Manager.
You will manage 1 Regulatory affairs specialist and report to the European Quality Manager.
Financial Accountability: While not a budget holder, responsible for supporting the Regulatory Affairs Manager in advancing the client's regulatory agenda.
Key Relationships/Interfaces: Externally represent the client with National Regulatory Authorities, Governmental Authorities, Industry Players, and Shareholders.
Internally collaborate with all client teams, especially the Commercial, Legal, and Finance teams.
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.
A leading financial services organisation is currently searching for a Head of Regulatory Reporting with experience in PRA and Financial Reporting on a 6 - 12 month contract basis.
The role will look to migrate to a perm role at the end of the contract.
The day rate will be £900 Umbrella per day, with their working policy being two - three days out of their London office.