Are you a Regulatory Affairs Specialist with in vitro diagnostic experience looking for a new contract role in the Franklin, MA area? This individual will serve as a subject matter expert for planning, coordinating, and implementing regulatory strategies for products requiring domestic and/or international governmental approval. Coordinate, support, and author clear and concise regulatory filings and responses for both domestic and international product registrations for in vitro diagnostic medical devices. Provides regulatory support on a range of activities which include domestic/international submissions, change assessments, quality system support, post market surveillance, and other compliance activities.
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Control exposures to hazardous chemicals & other safety hazards such as:
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About Ventura Solutions
Ventura Solutions is a reputable end-to-end medical device and combination product consulting, staffing, and training firm. With our deep industry expertise spanning medical devices and combination products, coupled with an outstanding talent pool, we stand out as the preferred option for a diverse array of projects. On the consulting side, we integrate seamlessly into your team and manage small to complex Statement of Work (SOW) projects. On the staffing side, we help source, screen, and on-board reputable employees to fill temporary, temp to permanent, and permanent job openings. We accelerate product development, keep products compliant, and help build great organizations. For more information, visit us at
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