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Advanced Resource Managers are currently partnered with a client based in Lausanne who are a leading marketer of consumer goods and operate on a global scale.
They are currently looking for additional support within their Regulatory Affairs department and require a Regulatory specialist to support them on a project on a 12 month basis. The role would be working within their portfolio of class IIa medical device products and the main focus will be to support the group whilst the Medical Device Regulations are in transition.
Reporting to the QMS & Regulatory Affairs manager EMEA, you are supporting all regulatory activities for the entire product portfolio however the main focus will be on the class IIa medical devices due to change of regulations.
Main duties in the role would be:
Qualifications for Consideration
The role is offering a competitive salary plus benefits package. This would be a fantastic role for a junior level candidate or a candidate with 1-2 years’ experience. If you are interested please contact Vik Patel at Advanced Resource Manager on 00442392 458031 or email me on email@example.com
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