Ensures systems are established that enable the manufacture of medicinal products in accordance with current national and international legislation, relevant standards and guidelines and the relevant Manufacturing and Marketing Authorisations.
Liaises as necessary with third party organisations and relevant Health Authorities to represent the Company interest and resolve Quality related issues.
Offer advice and guidance to the Company and its associates on issues relating to legislation, compliance and batch release.
Undertakes the duties of a Qualified Person as named in the manufacturing authorisation held by the company, as defined in EU Directive 2001/83.
Please quote Ref BARD/EM/NF04 when applying for this role. Closing date is 16/01/2018
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