A medical device company in Keele is looking for a Regulatory Affairs professional to assist in various regulatory activities. The role involves preparing and submitting documents for product registrations, assessing regulatory compliance impacts of design changes, and utilizing information systems to track registrations. The ideal candidate will have a Bachelor’s Degree in life sciences, strong organizational and communication skills, and a passion for learning about regulatory procedures in medical devices. Working hours are Monday to Friday, from 9 am to 5 pm.
#J-18808-Ljbffr