Regulatory Affairs Engineer
Cambridge
We're looking for a Regulatory Affairs Engineer for a contract role with a medical device manufacturer.
PicturaBio is building an early-stage QMS to underpin regulated IVD manufacture. The Senior Quality Associate will help develop and operate the eQMS (Greenlight Guru) and contribute to ISO 13485 compliance for UK and US regulation.
The role offers part-time hours (2-3 days per week) with potential to grow, and a clear path to Management Representative responsibilities as the QMS matures alongside the business. Location is Oxford, with pro rata competitive pay.
#J-18808-Ljbffr
Full job description from WhatJobs. Apply for this role →
Cambridge
We're looking for a Regulatory Affairs Engineer for a contract role with a medical device manufacturer.
Bristol
Salary: £50,000 – £55,000, depending on experience Location: Science Creates St Philips, Bristol Working pattern: Full time, 37.5 hours per week…
RH5 6QT, Wotton, Surrey
The Quality Assurance Associate will be instrumental in maintaining and improving the Quality management System at multiple manufacturing sites.…
Explore: Administrator jobs in Oxford Administrator jobs in the UK Specialist jobs in Oxford
Worked with Verifera as a candidate or employer? Your honest review helps the next person trust verified hiring.