Medtronic Regulatory Affairs Specialist Jobs in Kenya

Medtronic Regulatory Affairs Specialist Jobs in Kenya

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)

How to Apply

For more information and job application details, see; Medtronic Regulatory Affairs Specialist Jobs in Kenya

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