Posted by LHH Recruitment Solutions • £300/day to £450/day
Medical Underwriter - Flexible Working Available
Are you an experienced Medical Underwriter looking to make an impact in a leading financial institution?
Join our team and play a crucial role in delivering exceptional underwriting services within one of the UK's most trusted Life, Pensions, and Investments providers.
I am looking for a Technical Writer for an initial 5 week contract, daily rate will vary depending on experience between £300 - £450 for this remote role.
Robert Half are excited to be working on an interim opportunity for a completly remote based role.
You will need previous experience translating complex technical concepts into user friendly documents, working closely with the development & product teams to ensure accuracy.
Robert Half are excited to be working on an interim opportunity for our client based in Edinburgh.
I am looking for a Technical Writer for an initial 5 week contract, hourly rate will vary depending on experience between £23 - £26PH.
You will need previous experience translating complex technical concepts into user friendly documents, working closely with the development & product teams to ensure accuracy.
I am looking for a Technical Writer for an initial 5 week contract, daily rate will vary depending on experience between £300 - £450 for this remote role.
Robert Half are excited to be working on an interim opportunity for a completly remote based role.
You will need previous experience translating complex technical concepts into user friendly documents, working closely with the development & product teams to ensure accuracy.
SRG is working with a leading Biotechnology company based in the Edinburgh area who are looking for a Senior Regulatory Compliance Officer to join their team on a permanent basis.
The Senior Regulatory Officer is responsible to deliver end to end regulatory package under ODM-Distributor scheme in compliance with an established quality management system, overseeing initial compilation of design control evidences, supplier management, incoming inspection and product release process, product submission, post-market surveillance, vigilance and associated reporting
The Role
Preparing and compiling regulatory documentation, coordinating and executing regulatory submission in compliance with ISO13485, IVD 2017/746 Regulation, FDA 21 Code of Federal Regulations (CFRs), Medical Device Approvals (510(k)), and other country requirements as appropriate.