Regulatory Affairs Associate / RA Associate – Medical Devices

Job details

Regulatory Affairs Associate / RA Associate - Medical Devices - This is a fantastic contract opportunity for a Regulatory Affairs Associate / RA Associate to join a leading manufacturing company in the Kent area. The Regulatory Affairs Associate / RA Associate will hit the ground running and take a key role in ensuring the cost effective compliance of products, systems and procedures with regulatory requirements.

Regulatory Affairs Associate / RA Associate - key responsibilities:

• Tracking regulatory changes (standards / directives)
• Reviewing proposed changes for Regulatory impacts
• Compiling and reviewing departmental procedures
• Regulatory support to R&D products
• Preparing technical files and documentation
• Compiling RA documentation

Regulatory Affairs Associate / RA Associate - qualifications, skills and experience:

• Good educational background ideally including a degree qualification in science or engineering though this is not essential
• Comprehensive experience in a highly regulated industry sector such as Healthcare or medical devices
• Proven familiarity with the ISO 13485 Quality Management System, 21 CFR and cGMP, MDD
• Exceptional planning and organisation skills
• Effortless communication / interpersonal skills

This is a fantastic contract opportunity for a Regulatory Affairs Associate / RA Associate to join a leading medical devices manufacturer.

Apply now, send a full CV to p.rabey@x4group.co.uk or call Peter on 020 7836 3942 for more information