CPL Recruitment are actively recruiting for a Regulatory Affairs Supervisor within the medical device industry.
The Regulatory Affairs Supervisor will be responsible for the overall Regulatory Group and Document Control Department ensuring compliance to all relevant regulations. Potential candidates must have previous supervisory or people management experience. Quality systems experience and FDA experience are also essential for this role.
Please contact Lorraine at CPL on 051 511184 or email your cv to firstname.lastname@example.org.