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.
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.
As the Policy & Procedure Officer / Regulatory Affairs Compliance Officer you will assist in coordinating the policy and procedure framework for Operational teams, ensuring that all areas of compliance are covered.
Policy & Procedure Officer / Regulatory Affairs Compliance Officer who has exceptional writing skills, including copywriting, editing, and proofreading with accurate grammar and literacy is required to join a well-established housing association.
We have a fantastic new job opportunity for a Policy & Procedure Officer / Regulatory Affairs Compliance Officer who has exceptional writing skills, including copywriting, editing, and proofreading with accurate grammar and literacy is required.
As an experienced Regulatory Officer with solid SDS experience you will be involved and supporting all technical aspects of regulatory administration and support across the global business across Europe, Middle East and Africa region.
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 Yolk Recruitment Ltd • £40K/yr to £55K/yr
Yolk Recruitment is partnered with a pioneering medical device business during an exciting period of sustained expansion and has a new opportunity for a Regulatory Specialist to join the team.
The role offers not only the opportunity to be a part of a high growth, high innovation business in a rewarding field, but to make your mark in a lead role providing guidance on a wide range of regulatory affairs.
You'll support NPD projects, guiding others to ensure product compliance and support audits, developing RA strategies to govern the continued development of existing products as well as new product development as they continue to grow in existing and new markets.
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 Science & Technology Recruitment • £40K/yr to £50K/yr
General
An exciting opportunity has arisen for a Regulatory and Compliance Officer to join a well-established organisation based in the Southeast.
The role involves ensuring the company's compliance with external product regulations, market requirements, and third-party approvals and certifications.
Key Responsibilities
Manage product accreditation processes for national and international standards.