Position: Senior Grants and Trusts Lead (Fundraising)
Are you an experienced trusts fundraiser Are you passionate about inspiring, encouraging and challenging people of all ages and backgrounds to explore and understand the world around them If so, then apply now!
This role offers full or part-time working, flexible and hybrid hours.
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.
Posted by LHH Recruitment Solutions • £300/day to £450/day
Medical Underwriter - Flexible Working Available
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.
Are you an experienced Medical Underwriter looking to make an impact in a leading financial institution?
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.