Senior Regulatory Affairs Specialist Our client a Medical Device Multinational currently seeks a Senior Regulatory Specialist to join their team.
The Senior.
Regulatory Affairs Specialist will develop strategies and submissions for complex projects and issues related to regulatory documents, submissions, investigations, product development planning and regulatory agency interaction.
The Sr.
Regulatory position will assist in mentoring and development of staff members as part of the role.
Role/Responsibilities
• Manage Technical Documentation
• Manage global regulatory impact assessments
• Manage updates to global regulatory procedures
• Provide Regulatory support for R and to interface with all levels of management.
For further information contact James Cassidy or call in confidence **********