Looking to boost your electronic design career with a leading medical device company?
World leading innovation, capability and awesome company culture.
What you'll be doing:
Coordinate and associated technical documentation including,Specifications, Quality planning, Risk management planning and V&V planning.
Manage release of technical documentation and Design History Files to customers with approval of management as part of the project management process.
Create and issue Technical Documentation.
Plan and undertake process validation engineering
Collaborate with team to determine documentation requirements and generate content.
Provide feedback to management on documentation standards and procedures for management.
Prepare and edit technical documentation including review with stakeholders, including customers.
Understand, Implement and plan Engineering Systems to the relevant ISO 13485, CFR 820 standards and IVDR
Support customers and work with the project managers in the provision of design history file DHF, outputs from the System Engineering process.
Support Quality Audits with external auditors including customer audits in presenting and explaining the Systems Engineering approach, documentation and records
What's in it for you:
Popular technology domain to work in
Great team culture
Competitive salary package
Be part of this growing, evolving team. Apply Now!