At BioTalent, we are working with a client exclusively to fill their QA Manager position. They are a transformative Device company focused on developing new class 2 devices for a range of products

You will be responsible for establishing quality initiatives to support a new GMP facility

This role will offer you

• To work in a fast-paced environment and the ability to take a huge impact.
• To lead an existing team with further headcount being added over the next 6 months to double the team
• Exposure to high visibility from the senior leadership team.

You will be responsible for

• Quality Operational Activities from CAPA, NCR, Complaints, MDR and further
• Support both internal and external auditing in a front office facing role
• Further hiring into the team

You will bring the following

• Hands on Quality experience within a device or IVD products in an ISO13485
• Worked on Quality Operation activities
• Experience within CAPA, Post marketing, NCR, Complaint management
• Previous line management experience
• 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 michael.kakoullis@biotalent.com or on 857-990-4669 if you think you could be a good match.