Mdr - Regulatory Affairs Specialist

Pay 40-60/h depending on experience
Overview:
Engage with cross-functional team focused on MDR product remediation and/or implementation to establish global regulatory strategies, participate in creation and review of key product development deliverables and author regulatory documents (EU MDR Technical Documents).  Provide support to transition currently marketed products from EU MDD to EU MDR, including review of product/ manufacturing process changes, supplier changes, new and revised engineering protocols and reports, and product labeling. 
Top 3 things the manager is looking for:
Detail-oriented for review of product changes and documentation review, including labeling Prior experience authoring EU MDR Technical documentation and managing review with notified body Experience routing documents and changes through a controlled document control system Education Required: Bachelors in a scientific or technical discipline, engineering is preferred.
Years' Experience Required: Minimum of 3 years with advanced degree and Minimum of 5 years with a bachelor's degree