Senior Regulatory Affairs ExecutiveQT Instruments (s) Vietnam

Mô tả Công việc
Regulatory and Compliance Duties
· Oversee and track RA's team overall performance on business certifications and license applications and maintenance, product registrations' progress and maintenance.
· Manage the overall cost and budget for business licenses and certifications and new product registration and amendments.
· Perform business permit and licenses application and conduct maintenance including renewals and amendments.
· Perform product registration, renewals and amendments for all new and existing products including Medical Devices, Radioactive Products, Pharmaceuticals, Poison Drugs etc. and ensure compliance to regulatory authorities' requirements.
· Liaise with principals, local regulatory authorities and internal stakeholders on new product registrations, post registration maintenance and post market surveillance.
· Handle regulatory enquiries and issues relating to the sales and distribution of regulated products including customer complaints, adverse events etc and follow up to closure.
· To provide timely progress reports and budgeting information to Senior Manager, QRA.
Quality Assurance including Internal Process, Standardisation, and Improvement
· Led the QRA team and internal stakeholders in Goods Storage Practice (GSP) and Goods Distribution Practice (GDP) certification, ensuring process and documentation compliance.
· Manage and conduct customer and supplier audits and follow up till audit closure.
· Oversee the development, review and update of company's manuals and procedures including System Procedures, SOPs as per applicable international and local regulations and standards such as GSP and GDP, adhering to company's QMS requirements.
· Lead review of current processes such as product registration process with inter-department stakeholders and implement QRA continuous improvement projects to achieve harmonisation and standardisation.
Pharmacovigilance and Training
· Conduct Pharmacovigilance (PV) training, PV literature screening and provide relevant updates to stakeholders where applicable.
· Act as National Responsible Person for Pharmacovigilance (NRPP) as required per local PV legislation.
Other responsibilities
· Carry out any other duties assigned from time to time by Senior Manager, QRA.