Independently supervise, without any interference of third persons, manufacturing processes and control testing of the site, related to the drug manufacturing license, operating as Qualified Person according to the local law (Article 52 of the Legislative Decree n. 219 of April 24th 2006 from EU directive 2001/83/CE and following modifications). With respect to the quality of the medicinal products, assurance of compliance to the National Medicines Law and other applicable regulations and together with the Site Quality Head and Site Manager maintaining an effective implementation, monitoring and maintenance of a GMP-compliant quality system.
As Quality Assurance, it is required to support all GMP relevant tasks/issues (operational and strategic) by ensuring compliance according to the ADACAP internal quality standards, relevant regulatory requirements, filed product quality standards and SOPs in place
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