Investigation/Test Engineer- Reading- Perm- 32-38KAre you from a highly regulated industry? Experienced in Root Cause Analysis, CAPA and taking a part electo-mechanical devices? Looking for...
Are you experienced in regulatory affairs for devices and/or medicines? Would you like to add more variety to your skillset and branch out to medicines/device regulations? An established consultancy based in Hertfordshire are looking to add additional consultants to their close knit team.
Within each role, you will be managing multiple projects from prestigious clients across the globe. This will give you exposure to a wide range of devices and medicines, inclusive of IVD. The projects could range from a single piece of work to 24 months in length and your clients could call at any time for an update on the project. With this in mind, you need to ensure you're familiar with all of your ongoing work.
The vacancy in the devices team is for someone who has a strong devices background. This includes, clear understanding of ISO 13485 and MDR; proven experience of producing and updating technical files for class 1 and 2 devices and writing risk assessments. Exposure to medicines or an appetite to learn this side of the business, will be key to success.
The vacancy within the medicines team, is management role, leading a team of three. Management experience is not essential, but desired. A strong background in medicines regulatory work is essential.
Standard hours are 8:45 - 5:15, with core hours being 10:00-4:00. After passing your 3 month probation you will be granted one day per week to work from home. Fresh fruit is brought into the office weekly and the team attend social event such as festive activities and street food markets out of hours, if this is something that would take your fancy!
Salary is up for discussion, depending on your skills and experience.
Please apply today, if either of the above roles interest you... or if you're looking for a similar role in the UK.