Our client is a global biotechnology company specialising in the development of immunological products to diagnose and monitor patients with immunologically controlled diseases.
The role
An opportunity has become available for an Regulatory Specialist, experienced in Diagnostics, to join company and support the Global Regulatory activities in order to facilitate timely approval of new and existing products.
Posted by Wilsher Executive Recruitment • £30K/yr to £35K/yr
General
We are currently recruiting for two Regulatory Specialists to join a Milton Keynes based company, in a 1-year fixed term contract.
Overview
You will need to:.
The successful candidate will support internal customers including: Customer Service team, Sales reps, Research & Development team, and Quality Assurance team by serving as an expert in assigned areas.
We are partnered with a growing medical device manufacturer who are requiring a regulatory contractor on a 9 month basis.
Responsible for the creation, update and maintenance of all technical files in support of obtaining and maintaining Notified Body CE certification, FDA clearance, and UKCA marking.
This is an urgent position and ideally is looking for the right person to start immediately.
FPSG are supporting our established global client with an exciting opportunity for a Request for Proposal /Regulatory Specialist on a 12-month temp role, based in London.
As RFP specialist you will support will support the Investment Management Sustainability team in collecting, drafting and consolidating related content for RFPs, DDQs, and other external reporting requirements.
Your responsibilities will include
Drafting, coordinating and completing Request for Proposals (RFPs) and responding to Due Diligence Questionnaires (DDQ) requests.
This consultancy is looking to strengthen their Regulatory Labelling group by taking on an experienced Regulatory Affairs Labelling professional for a contract job.
Seeking a Contract Responsible Person for Medical Device Sector in South East England
In this role, you will be responsible for ensuring that all regulatory requirements related to Good Distribution Practice (GDP) guidelines are met, including conducting audits and vendor qualifications.
Our client is a leading medical device company located in South East England, and is seeking an experienced and highly motivated individual to join their team as a Contract Responsible Person.