Regulatory affairs associate - united kingdom, crewe, cheshire
excellent opportunity to provide regulatory expertise in the research, development and marketing of products.
client details
my client is a leading medical devices manufacturer within the advanced wound care and consumer healthcare product space.
description
the ra associate will provide regulatory expertise in the research, development and marketing of products. the role holder will prepare regulatory submissions and ensure regulatory approvals are obtained and maintained within project registration plans and the needs of the business.
profile
you will have
higher degree in medical, biological or chemical sciences preferred.
must have experience in medical device regulatory affairs, post market surveillance, quality assurance or design control or related function.
experience of medical device registration in global markets including canada, brazil, australia, middle east, and far east would be an advantage.
experience in medical device registration including eu or usa would also be an advantage.
job offer
competitive package available
Apply to this job now Report abuse