Part of Phaidon International
Part of Phaidon International
Showing 11 results
Sort by:
Senior Validation Engineer (Contract)Location: Hertfordshire (Hybrid/On-site as required) Contract: 6+ Months Industry: Medical Devices / Life Sciences We're supporting a medical device manufacturer through a significant operational expansion and product transfer project within one of its key UK sites.As part of a large scale investment in manufact...
Job Description - Automation / Electrical Controls Engineer (Contract)📍 LocationPortsmouth, UK (on-site)📅 Contract Type & DurationContract role (outside IR35 / SoW-based)Approx. 18-19 month engagement (through to end of 2027)Start date: ASAP🚀 OverviewWe are seeking an experienced Automation / Electrical Controls Engineer to support the developme...
Responsible Person (RP) ConsultantLocation: London (Hybrid) Contract: Part-Time We are currently partnering with an established organisation operating within the Medical Device and Life Sciences sector that is seeking an experienced Responsible Person (RP) to provide specialist quality and compliance support on a contract basis.This is an excellent...
Take the first step toward your next opportunity - submit your resume and get started today.
EPM Scientific are partnered with a Global Diagnostics Manufacturer to hire a Sr. Regulatory Affairs Specialist primarily supporting Performance Study Applications for CDx programs to EU Competent Authorities and/or MHRA via CRO.This is a 12 month, full time contract, starting ASAP. Remote with occasional on site presence in the north of England id...
Test Validation Engineer We're supporting an innovative medical technology company that is looking to hire a Test & Validation Engineer to lead verification and validation activities across a cutting-edge medical device platform.This role will play a key part in supporting regulatory approvals, taking ownership of testing activities across hardware...
Develop and execute Medical Information strategies , including annual planning, launch support activities, insights analysis, response development, review, and approval management.Lead strategic publication planning across assigned products, creating and maintaining annual publication plans based on stakeholder input, study data, scientific eviden...