Newton Colmore Consulting is seeking a Regulatory Affairs Engineer for Cambridge, to support medical devices across diverse projects. You will work at the intersection of design, innovation and compliance, partnering with design engineers, scientists and project teams to ground development in robust regulatory thinking.
You will apply ISO 9001, ISO 13485 and FDA 21 CFR 820 knowledge, develop regulatory strategies, interpret requirements, track changes and contribute to the quality management
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Regulatory Strategy Engineer – Medical Devices in Cambridge employer: Newton Colmore Consulting
As a Quality Assurance Specialist at this innovative Medical Devices company in Cambridge, you will be part of a dynamic team dedicated to developing high-quality products that make a difference in healthcare. The company fosters a collaborative work culture, offering ample opportunities for professional growth and training in ISO 13485 standards, making it an ideal environment for both early-career professionals and those looking to expand their expertise. With the potential for hybrid working arrangements as you progress, this role not only promises meaningful work but also a supportive atmosphere where your contributions are valued.
