At BioTalent, we are working with a client to fill their newly created QA specialist position. They are a transformative Device company focused on large range of products with a large customer base
This role will offer you
* To work in a fast-paced environment and the ability to take a huge impact.
* Work closely with their RP
* A chance to work across a global quality system
* Exposure to high visibility from the senior leadership team.
You will be responsible for
* Support both internal and external auditing in a front office facing role
* Lead QMS updates
* Support documentation updates including risk management and design history files
* Coordinate GDP documentation
You will bring the following
* Hands on Quality experience within a device or IVD products in an ISO13485. Ideal candidates will have experience in pharmaceutical.
* Worked on internal audits
* Previous track record of updating QMS
* Experience within GDP
* Experience within CAPA, Post marketing, NCR, Complaint management
* BSc or MSc in a relevant Life Sciences subject
If you want to be part of an innovative thinking, growing company where you can grow and expand your current knowledge, GET IN TOUCH - Please email me at or on if you think you could be a good match.