Medical Device Regulatory Affairs Job Description
Apply to regulatory specialist and more.
Medical device regulatory affairs job description. Medical device companies also rely on their regulatory affairs team after a device is cleared or approved. The duties and responsibilities of regulatory affairs specialists have expanded in recent years as a result. Familiarity with medical device or diagnostics industry standards and regulatory requirements e g. These departments can be found in a variety of companies that manufacture pharmaceuticals drugs medical devices cosmetics and industrial chemicals.
They may also work in government or law. Apply to regulatory specialist medical device regulatory affairs development rad program senior engineer and more. Regulatory affairs associates are often employed by pharmaceutical or medical devices companies and assist in obtaining government approval for drugs medical devices veterinary products cosmetics and foods. Regulatory affairs officers act as a link between companies and regulatory authorities ensuring that products are manufactured and distributed in compliance with appropriate legislation.
Regulatory affairs specialists assist in obtaining and maintaining government approval for drugs medical devices nutritional products and related materials. The organisation for professionals in regulatory affairs explains on its website that a. Regulatory affairs associates occupy one career niche within the larger regulatory affairs profession which exists in many industries. Qsr iso13485 2017 745 2017 746.
30 days ago save job not interested report job. Regulatory affairs is a comparatively new business administration function. Apply to regulatory affairs manager quality assurance manager senior safety manager and more.