Brecon appoints director of QA and regulatory affairs

Kay O’Hagan will head a team of Qualified Persons

Brecon Pharmaceuticals, a supplier of commercial packaging and clinical trials supply services for the pharmaceutical and healthcare sectors, has appointed Kay O’Hagan as director of quality assurance and regulatory affairs.

O’Hagan joins the Hay-on-Wye, UK-based firm from a major pharma multinational, where she was head of quality assurance. A microbiologist by training, she has broad experience in research and development, production, quality control and quality assurance.

O’Hagan takes responsibility for Brecon’s QA and regulatory activities, and will head a team of Qualified Persons.

‘QPs are in great demand in the industry and I am delighted to be given the opportunity to work with the four QPs at Brecon on the complex task of releasing various companies’ products into the current market. It will be a challenge – but one I am really looking forward to,’ she said.

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