One of our key clients is a leading supplier in the defence and aerospace sector and they’re currently looking for an SC cleared technical author who’s able to work a 3 month contract on one of their sites in New Malden….
Job Title: Police Staff InvestigatorContract Length: 5 MonthsRate NegotiableA law enforcement client in the North West of England are looking for 6 experienced investigators to support in major investigations across the…
Waste Certifier Nayr Recruitment are currently looking for a Waste Certifier based in Thurso (onsite at least once a week so must be local) for a 12 months temp contract. Role: Waste Certifier Digital/Non Digital – Non C…
I am recruiting for one of the leaders in professional services to the Data Centre’s, Life Sciences, Pharma and Manufacturing sectors globally. They are in expansion mode, hence the demand for talented Project Controls/P…
I am recruiting for one of the leaders in professional services to the Data Centre’s, Life Sciences, Pharma and Manufacturing sectors globally. They are in expansion mode, hence the demand for talented Project Controls/P…
My client is a global medical device manufacturer, who globally provide medical technologies designed to improve the health and quality of people’s lives around the worldJob DescriptionApply technical solutions to proble…
Every day, our mission is to make sure that pets enjoy an active life, for their whole life. We are the experts in scientifically backed pet supplements with the UK’s No.1 joint supplement brand, YuMOVE, now supporting w…
My client is an international medical devices business, developing, manufacturing, and commercialising easy to use and accurate molecular diagnostic solutions for reproductive health.Job DescriptionThe maintenance of Tec…
My client is a leader in generic and biosimilar medicines and a pioneer in digital therapeutics.Job Description Your responsibilities as Regulatory Affairs Manager include, but are not limited to: Timely and accurate pre…
My Pharmaceutical client specialises in the licensing and marketing of generic pharmaceuticals and is focused on growth through product launches and EU expansion. There ambition is to grow there commercial structure in E…
My client is an international molecular diagnostics company, working in partnership to advance diagnostic science.Job DescriptionThe creation, management and maintenance of Technical Files for the product range in accord…
Fast growing business with excellent opportunitiesJob Description – Preparing submission documents- Leading agency interactions – Leading overall Regulatory Affairs strategy- Internal/External stakeholder engagement- Lea…
I have partnered with a market leading and rapidly expanding consultancy who due to growth are looking for a number to regulatory affairs professionals to join the high performing Regulatory Affairs team.The role can be…
My client is a global Medical Device manufacturer that provides medical devices that are designed to improve the health and quality of people’s lives around the globe.Job DescriptionApply technical solutions to problem s…
My client is medical imaging company with a strong focus on precision medicine using advanced imaging and genetics,Job Description As Regulatory Affairs Specialist you will assist in the preparation and submission of reg…
My client is a Quality & Regulatory Affairs specialist Consultancy business, providing clients technical and specialist support across Medical Devices & IVDs.Job DescriptionProvide consultation on regulatory standards, d…
My client is a global medical device business providing a range of products within wound and skin care.Job DescriptionCreation, and maintenance of high quality regulatory compliant documentation, as needed for all classe…
My client are a fast growing innovative and exciting pharmaceutical business who focus on rare metabolic and neurological genetic conditions. We are looking for a Head Of Global Regulatory Affairs to be based out of the…
One of the largest global medical technology companies, addressing some of the most challenging global health issues.Job DescriptionExecute transition of MDD tech files to MDR Technical Documentation, monitor and report…
Rapidly growing pharmaceutical service provider who specialise in Early Access Programs.Job Description Head Of Regulatory Affairs – EAPThe Head of Regulatory Affairs will report to the Managing Director EU.The role will…