Regulatory Affairs Specialist at Medtronic

A Day in the Life

• Performs coordination and preparation of document packages for regulatory submissions from all Operating Units and departments for countries across the region
• Compiles all materials required in submissions, license renewal and annual registrations.
• Networks across departments to ensure that products are approved for the market
• Monitors and improves tracking / control systems.
• Keeps abreast of regulatory procedures and changes.
• May direct interaction with regulatory agencies on defined matters.
• Performs post market requirements

Must Haves

• Minimum 3 years experience in regulatory affairs
• Ability to communicate effectively to all levels of the organization and customers in English (strong written and verbal skills)
• Strong MS office skills
• Ability to work co-operatively in a matrix environment
• Capability to establish and use networks to acquire information

Nice to Haves

• SAP, Insight experience

We Offer

We offer a competitive salary and benefits package to all our employees:

• Flexible working environment
• Annual Incentive Plan % depending on company results
• Pension scheme and group discount on healthcare insurance
• Training possibilities via Cornerstone/Harvard Manage Monitor/Skills Lab
• Employee Assistance Program and Recognize! (Our global recognition program)