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Associate Director, Quality Assurance, Singapore Plant

The employer is a global, research and development-driven pharmaceutical company committed to bringing better health and a brighter future to patients Lead the QA team in ensuring that an effective Quality Assurance oversight is provided to the site. Provide leadership and technical support for all GMP/quality activities for manufacturing and other assigned areas of responsibility. Lead the QA team to establish, disseminate and monitor the implementation of appropriate quality systems and compliance standards for the site according to regulatory, corporate and division requirements. Responsible for ensuring that product quality issues are correctly investigated and that appropriate corrective and preventative actions are implemented. Proactively monitor sources of trends, complaints, failures, deviations and changes to identify opportunities for system, process and product improvements. Support the compliance, regulatory and training activities as required and any other responsibilities as assigned by Site Quality Head.a Degree in pharmaceutical sciences, life sciences, biology, biotechnology chemistry, chemical engineering, or a related discipline. Additional certification and trainings such as auditor training or QP training will be advantageous. Minimum experience of 10 years, with 5 years of supervisory position, in the pharmaceutical or biotechnology in quality assurance, GMP/GLP compliance, operations or validation, ideally in a multinational company. FDA/Eu cGMP know-how and a thorough understanding of ICH guidelines, together with exposure to the international regulatory network. Able to logically solve problems in order to find timely solutions. An ability to interact and communicate with all types of personalities in an effective and diplomatic manner. Ability to collaborate cross functionally and cross sites. Good decision making capability.