- QA Engineer – Medical Devices – 6 months – Leiden area
Currently, I am recruiting for one of my most prestigious clients, based in the Benelux area. They're amongst the top leaders in their niche industry, specializing in medical devices within the diagnosis and therapy market. Now that their products are focussing more and more on biographic and biometric traits, they have grown even more over the last year, since this has opened so many new markets for them. ...
- Quality Engineer
Here at ProClinical, we have a Quality Engineer position that has opened up at a global Medical Device Contract Manufacturer providing manufacturing needs to the Medical Devices industry. With manufacturing sites in over 80 different locations worldwide, this company provide innovative ideas behind multiple sectors. This particular position will be based in Ireland. ...
- Validation Specialist / Validation Engineer
The successful candidate will You will be working with my clients Production, QA and R&D departments to validate existing equipment, processes, data and documentation ready for the transfer to the companies new HQ which is currently under construction.
- Computer System Validation Engineer / CSV Engineer
My client, a global specialist pharmaceutical company based in the South of England are seeking a Computer System Validation Lead (CSV).
- Senior Process Validation Engineer - MedTech - exciting startup
Senior Process Validation Engineer - MedTech - English language - exciting startup in NetherlandsWorking on cutting edge technology for cardiovascular products, our client is aiming to be the clear leader in their field. With sites across Europe, their production facility in the Netherlands is needing a senior process validation engineer to help them in their cause.English is the day to day language at this site.
- Site Contracts Associate II with Top 10 CRO - Netherlands/Belgium region - 0% travelling role
A top 10 CRO is looking to employ a Site Contracts Associate II in the Netherlands/Belgium region to support site contracting activities. An ideal role for Senior CRAs looking to reduce travel time as part of general responsibilities.
- Regulatory Affairs Specialist - Medical Device - Contract
I am currently seeking a Regulatory Specialist with at least 2 years’ experience to join a leading, multinational medical device company based in Bedfordshire (South East of England) on a contract basis.
- Senior Pharmacovigilance Officer / Senior Drug Safety Officer - Hertfordshire/South East
I am currently looking for a Pharmacovigilance professional with at least 1 years' experience to join a market leading pharmaceutical company based in Hertfordshire (South East of England). The role will primary work with Case processing and QC'ing of ICSRs but also offers exciting opportunities for development/progression with the department.
- Regulatory Affairs Manager - Clinical Trials
I am currently seeking a Regulatory Affairs Clinical Trials Manager to join a leading, global pharmaceutical company based in Berkshire for a 6-12 month contract.
- Senior Regulatory Affairs Officer/Senior Regulatory Affairs Associate
I am currently seeking a Senior Regulatory Affairs Officer to join a global specialist Pharmaceutical & Medical Device Company in a brand new state of the art facility based in Maidenhead. 12 Month FTC offering a salary of up to £45,000 + bonus + benefits