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.
They are looking for an individual that is hard working and self motivated to assist with all things regulatory.
Responsibilities will include: Oversee the development and management of technical files, dossiers, and regulatory documents for medical devices and pharmaceuticals.
To act as a deputy to the Head of Regulatory Affairs, supporting day-to-day compliance activities, managing the Compliance team, attending meetings, producing reports and deputising as required.
A specialist Insurance MGA is currently recruiting for an experienced Compliance Manager to join their growing team in London
Key tasks
Act as a deputy to the Head of Regulatory Affairs in the delivery of the compliance plan, including associated monitoring and reporting.
Our medical manufacturing client in Taunton is seeking an experienced Regulatory Affairs Administrator to join their team.
About the Client
A well established and respected Manufacturer of medical devices and instrumentation.
With over 100 years' experience in the healthcare market, they aim to consistently offer high quality, cost effective equipment that meet the needs of today's ever-changing healthcare sector.
Posted by Nashrock Recruitment • £90K/yr to £100K/yr
General
The Compliance Manager will serve as the deputy to the Head of Regulatory Affairs, supporting day-to-day compliance operations, managing the Compliance team, attending key meetings, preparing reports, and stepping in when needed.
Direct Reports: Senior Compliance Analyst, Compliance Assistant, Compliance Monitoring Assistant
Posted by WALKER COLE INTERNATIONAL LTD • £80K/yr to £100K/yr
Walker Cole is seeking a Senior Manager of Regulatory Affairs to join a clinical-stage biopharmaceutical company based in the South of England.
This position has become available for a European and UK Regulatory Lead to oversee regulatory strategy for immunotherapeutic products at all development stages.
Key responsibilities include creating plans for clinical and non-clinical regulatory submissions that align with project goals and working with the Regulatory CMC and Operations teams to ensure plans are coordinated and implemented effectively.
Posted by Science Solutions Recruitment Ltd • £27K/yr to £35K/yr
This is to work as a Regulatory Affairs Officer to progress your career within a Parallel Import company.
This position is open to both Regulatory Officers from either a Pharmaceutical GMP background, or ideally a Pharmaceutical GDP parallel import background.
A great opportunity has arisen withing a Birmingham based pharmaceutical company.