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Our client, a global pharmaceuticals manufacturer based in Connacht, now seeks a Regulatory Affairs Specialist who will perform primary review of CMC sections of regulatory submissions and develops relationships with other departments and the Regulatory Agencies to assist in the definition of CMC regulatory strategy.
An opportunity has arisen with our client based in Waterford for a Regulatory Affairs Specialist on a 12 month contract basis. Continuous Improvement of Regulatory Affairs processes and procedures - Review and evaluate the regulatory impact of proposed changes at the site.
The Senior Regulatory Affairs Specialist is to support department goals and continuous improvement initiatives, prepare and support vigilance on regulatory data related to the company’s range of medical devices. Key requirements of Senior Regulatory Affairs Specialist
My client a medical devices company in the Midlands is currently looking to recruit a Senior Regulatory Affairs Specialist to join their RA function due to growth. Support vigilance on regulatory data for a range of medical devices - Ensure continued compliance to regulatory requirements by interpretation of new medical device regulations