Regulatory Affairs Specialist
2 weeks ago
Job Title - Regulatory Specialist II
Location - 10 Southgate Road, Scarborough, ME 04074
Duration – 6+ months of contract role
Pay rate $59/hr on w2
Job Description
Years Experience: 2-5 years regulatory experience and/or 2 years relevant industrial experience typically with a quality, product-development/support, or scientific affairs function Skills: Knowledge of regulations and standards affecting IVDs and/or biologics Education: BS preferred in a technical discipline like biology, chemistry, microbiology, immunology, medical technology, etc.
Duties: Responsible for implementing and maintaining the effectiveness of the quality system. Supports manufacturing/operations day-to-day activities for change control. Provides consultation/advice to regulatory specialists for change control and product development. Provides regulatory direction/interpretation on team activities. Interprets and applies regulatory understanding to support products and teams. Prepares U.S. regulatory submissions and/or registration documents for international affiliates and government agencies worldwide. Handles regulatory activities involved in documentation, labeling, and field support. Applies regulatory and technical knowledge to a wide variety of complex work assignments. Maintains and ensures compliance to the appropriate quality system for the specific medical device(s) designed or manufactured that the individual supports. Ensures compliance to and is able to demonstrate knowledge of site and division-level policies and procedures.
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Regulatory Affairs Specialist
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Regulatory Affairs Specialist
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