Regulatory Affairs Supervisor

Regulatory Affairs Supervisor Location: Littleport, Cambridgeshire - CB6 1SE Salary: £45k + Benefits Contract: Full time, Permanent Hours: 37.5 pw Benefits: 25 days holiday a year plus bank holidays, increases with length of service Company pension scheme, minimum 4% contribution Private healthcare after successful completion of the probationary...

Regulatory Affairs Supervisor Location: Littleport, Cambridgeshire - CB6 1SE Salary: £45k + Benefits Contract: Full time, Permanent Hours: 37.5 pw Benefits: 25 days holiday a year plus bank holidays, increases with length of service Company pension scheme, minimum 4% contribution Private healthcare after successful completion of the probationary...

Regulatory Affairs Supervisor Location: Littleport, Cambridgeshire - CB6 1SE Salary: £45k + Benefits Contract: Full time, Permanent Hours: 37.5 pw Benefits: 25 days holiday a year plus bank holidays, increases with length of service Company pension scheme, minimum 4% contribution Private healthcare after successful completion of the probationary...

Regulatory Affairs Supervisor Location: Littleport, Cambridgeshire - CB6 1SEScroll down to find the complete details of the job offer, including experience required and associated duties and tasks.Salary: £45k + BenefitsContract: Full time, PermanentHours: 37.5 pw Benefits: 25 days holiday a year plus bank holidays, increases with length of service...

Regulatory Affairs SupervisorLocation: Littleport, Cambridgeshire - CB6 1SESalary: £45k + BenefitsContract: Full time, PermanentHours: 37.5 pwBenefits: 25 days holiday a year plus bank holidays, increases with length of service Company pension scheme, minimum 4% contribution Private healthcare after successful completion of the probationary period Death in...

We are currently looking for a Regulatory Affairs Specialist to join a leading Medical Device company based in the Cambridgeshire area. KEY DUTIES AND RESPONSIBILITIES: Your duties as the Regulatory Affairs Specialist will be varied however the key duties and responsibilities are as follows: 1. Make sure all the technical medical device files and the QMS is...

A growing Biotech company in Cambridgeshire is looking for a Regulatory Affairs Specialist, to support the Regulatory team. **As a Regulatory Affairs Specialist, you will**: - Compile and review medical device files for the company's products; - Produce documentation supporting regulatory submission to comply with regulatory authorities; - Work with the...

Proclinical is seeking a dedicated and detail-oriented individual for the role of Regulatory Affairs Manager. This role offers an exciting opportunity to manage a subteam within the Regulatory Department, providing exposure to various aspects of regulatory affairs from clinical trials to lifecycle management in medicines and medical devices. ...

An innovative global pharmaceutical company is currently looking for a Regulatory Affairs Manager with CTA, UK/IE and early stage development experience to join their team on a 12 month temporary contract. Working with the regulatory team (and core stakeholders across multiple areas), your role will be to provide regulatory strategy and guidance across the...

An innovative global pharmaceutical company is currently looking for a Regulatory Affairs Manager with CTA, UK/IE and early stage development experience to join their team on a 12 month temporary contract. Working with the regulatory team (and core stakeholders across multiple areas), your role will be to provide regulatory strategy and guidance across the...

Your New Company: Join this renowned biopharmaceutical organisation dedicated to developing innovative therapies that improve patients' lives. Leaders in the industry and looking for a biologics CMC Regulatory Affairs contractor on a 12-month assignment. Your New Role I am seeking a Regulatory Affairs Manager - CMC (Biologics) for a 6-month contract for...

Your New Company: Join this renowned biopharmaceutical organisation dedicated to developing innovative therapies that improve patients' lives. Leaders in the industry and looking for a biologics CMC Regulatory Affairs contractor on a 12-month assignment. Your New Role I am seeking a Regulatory Affairs Manager - CMC (Biologics) for a 6-month contract...

Executive Director, Regulatory Affairs Labeling page is loaded Executive Director, Regulatory Affairs Labeling Apply locations United Kingdom - Cambridge United Kingdom - Uxbridge posted on Posted 2 Days Ago job requisition id R0041368 For Current Gilead Employees and Contractors: For more than 35 years, we’ve tackled diseases such as HIV, viral...

Executive Director, Regulatory Affairs Labeling page is loaded Executive Director, Regulatory Affairs Labeling Apply locations United Kingdom - Cambridge United Kingdom - Uxbridge posted on Posted 2 Days Ago job requisition id R0041368 For Current Gilead Employees and Contractors: For more than 35 years, we’ve tackled diseases such as HIV, viral...

Regulatory Affairs Labelling Manager This consultancy is looking to strengthen their Regulatory Labelling group by taking on an experienced Regulatory Affairs Labelling professional for a contract job. As the Regulatory Affairs Labelling Manager, you would be responsible for developing the strategy and leading the development and update of core labelling...

An innovative global pharmaceutical company is currently looking for a Regulatory Affairs Manager with CTA, UK/IE and early stage development experience to join their team on a 12 month temporary contract. Working with the regulatory team (and core stakeholders across multiple areas), your role will be to provide regulatory strategy and guidance across the...

An innovative global pharmaceutical company is currently looking for a Regulatory Affairs Manager with CTA, UK/IE and early stage development experience to join their team on a 12 month temporary contract. Working with the regulatory team (and core stakeholders across multiple areas), your role will be to provide regulatory strategy and guidance across the...

An innovative global pharmaceutical company is currently looking for a Regulatory Affairs Manager with CTA, UK/IE and early stage development experience to join their team on a 12 month temporary contract. Working with the regulatory team (and core stakeholders across multiple areas), your role will be to provide regulatory strategy and guidance across the...

An innovative global pharmaceutical company is currently looking for a Regulatory Affairs Manager with CTA, UK/IE and early stage development experience to join their team on a 12 month temporary contract. Working with the regulatory team (and core stakeholders across multiple areas), your role will be to provide regulatory strategy and guidance across the...

Associate Director - Regulatory Affairs page is loaded Associate Director - Regulatory Affairs Apply locations United Kingdom - Cambridge time type Full time posted on Posted 17 Days Ago job requisition id R0040532 For Current Gilead Employees and Contractors: Please log onto your Internal Career Site to apply for this job. At Gilead, we’re creating...