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Form of workBrightwork are supporting with the recruitment of a Senior Regulatory Affairs Associate to join one of our prestigious clients on a Full Time, Permanent Basis with an Immediate start.
This is a remote working role, perfect for someone who is willing to travel to the clients office in Glasgow from time to time.
Duties include:
Support regulatory projects as required
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Support writing technical/submission documents for Custom devices, CE devices and international registrations as required
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Support CAPAs and SATs from initiation to closure as required
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Review and maintain product approval certification database as required
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Prepare regulatory submissions for product approvals as required
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Prepare Custom Made device, Special Products paperwork and change impact assessments as required
• Other duties as required by Regulatory Affairs department
The successful candidates will have Regulatory or Quality experience within a medical device or pharma environment
Brightwork Ltd offers the services of an employment agency for permanent work and an employment business for temporary work
