Overseeing the release of medicinal products for distribution, ensuring compliance with all relevant regulations and guidelines. Reviewing and approving batch records, analytical data, and other documentation related to the manufacturing and testing of medicinal products. Investigating and resolving quality issues and deviations related to manufacturing processes and materials. Participating in internal and external audits of the manufacturing facilities and quality systems. Providing expertise and guidance on regulatory requirements and quality standards to internal teams. Please note that we will be interviewing throughout the duration of this advert. Therefore, if you are interested in this role, an early application is advised as we may close the advert prior to the advertised date. The ideal candidate for this role will have a strong background in pharmaceutical manufacturing, quality assurance, and regulatory compliance, and have excellent attention to detail and problem-solving skills. As a minimum, you should hold a third-level qualification in a scientific discipline – pharmacy, medicine, chemistry, pharmaceutical chemistry, or biology. In addition, you must have fulfilled the education requirements for the role of the Qualified Person, such as a diploma in Pharmaceutical Manufacturing Technology. Previous Experience:
A minimum of 3 years practical experience in activities of quantitative and qualitative analyses of active substances and of the necessary testing and checking to ensure the quality of medicinal products.
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