Regulatory Affairs Specialist X 2

Hartley People Recruitment

Wexford

The Role Ensuring compliance with FDA Quality System Regulation, Medical Device Directive. Assist with regulatory submissions. Assist with preparation activities for FDA inspections and internal audits. Process customer regulatory requests. Support Quality system improvements and regulatory activities concerning the Quality system. Coordinate internal Audit system. The Person Strong planning and coordination abilities. Strong attention to detail. Experience of working to deadlines and also on own initiative. Exemplary interpersonal skills. Up to 3 years experience in a quality assurance role in the pharmaceutical, healthcare or medical device sector, preferably in an FDA regulated environment. Engineering, Science related Degree or equivalent experience. Hartley People Recruitment work to the highest ethical standards within our industry and we value the trust that you place in us when you send your CV. We can provide a full consultation in confidence and we guarantee that your CV will not be sent to any of our clients without your prior consent. For immediate consideration please call Sara on 051-878813 or email your CV in response to this job posting sarabrennan@hartleypeople.com. Hartley People also recruit for similar roles such as Regulatory Specialist, Compliance Auditor, Compliance Officer, Regulatory Officer, Regulatory Manager, Senior Regulatory Manager, Regulatory Assistant. This job originally appeared on RecruitIreland.com.

2942 days ago