What the role is:This position serves to support the Audits Branch (AB) in implementing the regulatory inspection and licensing regime, policies and initiatives governing the full spectrum of dealers across various health product categories in Singapore so as to meet HSA's national objective of ensuring that these health products meet the required standards of quality, safety and efficacy to safeguard public health and safety.i)Lead the conduct or conduct of local/overseas regulatory inspections and licensing of manufacturers and dealers of health products and pharmacies ensuring that they conform to Good Manufacturing Practice (GMP), Good Distribution Practice (GDP), regulatory requirements and other relevant quality system standards.ii)Lead/assist in the review of regulatory policies and legislations related to manufacturers and dealers of health products and active ingredients and the translation into specific technical and operational plans for implementation to achieve the desired outcome.iii)Lead/assist in the review, development and implementation of technical standards, industry guidelines, internal good practice guidance on GMP inspectionsiv)Lead/assist the effective implementation of the AB's Quality Management System (QMS) in accordance with Phamaceutical Inspection Co-operation Scheme (PIC/S), ISO 9001 standard and other international standards, e.g., WHO ML4 & WLA.v)Lead in/assist in the management and handling of stakeholders' technical and procedural enquiries.vi)Lead in/assist with performing assessment of changes (URS, UAT, etc.) to electronic processing systems for inspection and licensing.vii)Lead/assist in the inspection scheduling and monitoring of performance indicators related to inspections.viii)Assist the Branch Director and Unit Deputy Director in ensuring that there are effective mechanisms in place to capture, store and communicate key information, experience and knowledge gained by the inspection teams.ix)Work in collaboration with international colleagues to facilitate technical liaison with other regulatory authorities and relevant bodies in the field of GMP inspection.x)Perform such other duties as the department may reasonably require.Job Requirements
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