Regulatory affairs and QMS Officer (part time)
Our North West based client develops and manufactures a range of medical device products, up to and including class 3 devices. They are actively looking for a Regulatory and QMS Officer for immediate start.
The primary function of this role will be document control within the regulatory/quality department for their ISO systems including ISO:9001 and ISO:13485
Applications are invited from candidates with a BSc in a related field together with some experience in the pharmaceutical or health care industry in a regulatory affairs position. Experience with Type 2B medical devices is required as a minimum, with good knowledge of ISO 13485.
Role: Permanent (part time 3 days a week)
Salary: Competitive dependent on experience
Location: North West England
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