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As a Senior Regulatory Affairs Specialist, you will be a key member of our Regulatory Affairs group. Position: Senior RA Specialist – Midlands - You will maintain site Regulatory Affairs compliance, based on cGMP per requirements as defined in FDA 21CFR820, ISO 13485, MDD, CMDCAS, IEC 60601, and other International Regulations.
Regulatory Affairs Specialist Quality Contracts in areas of Validation, Regulatory, Compliance & CAPAS. * Compliance Specialist For more information on our Recruitment and HR Services and to see a full list of our available jobs across Ireland, please visit our website