(SN-125) - REGULATORY PROJECT ASSOCIATE

Sólo Para Miembros Registrados


Job summary We're committed to delivering medicines to the world with greater speed, without compromising on excellence and integrity. Navigating both local and global regulations is crucial, and the dynamic regulatory landscape demands innovative thinking and meticulous attention to detail. Your contributions will ensure that our products meet the highest standards of regulatory compliance, ultimately helping patients receive the treatments they need more efficiently. JOB RESPONSIBILITIES - Preparation and management of relevant monthly reports and communications. - Analytical and operational related support for related systems/processes (including SPA reporting, RRM maintenance, CST requests, Veeva, product milestone and departmental metrics tracking, Reliability Performance, Reg21, etc.) - Ensure that regulatory documentation meets relevant regulatory requirements. - Work in collaboration across the organization with stakeholders to deliver efficiencies in regulatory submissions and processes. - Support any special project as requested by manager or support departments managers/designee. - Knowledge and understanding of quality systems, processes, audit and inspections. - Ability to influence at all levels in the organization and build networks internal and externally. General Support - Provide a full range of operational support to the GRS-EM-RIO Organization. - Ensure regular liaison with department managers to assess workload and priority activities. - Make arrangements and coordinate meeting/conference/training activities to ensure information on venue, time and people is communicated in advance. - Prepare and distribute minutes of meetings when required. - Organize travel arrangements for teams/visitors (Pfizer colleagues from overseas) as required. - Liaise with the travel agency or manage Pfizer global booking system (e.g. PT&E;) to arrange air tickets, itinerary and book accommodation. - Obtain requirements for the trip - equipment, visa, travel approvals and travelers cheque. - Assist Departments in creating or raise purchase orders electronically for goods and services. - Generate quotations and purchase orders. - Ensure the payment of all invoices in a timely manner. QUALIFICATIONS / SKILLS - Degree in Business Administration or related discipline. - +3 years of experience in administrative/operational role. - Working experience in a regulatory affairs environment. - Fluent in English – written and spoken communication skills. - Meticulous nature and proficient in data tracking and consolidation. - Ability to work independently and as part of a team. - Proven ability to consistently deliver to time, cost and quality standards. Descripción del trabajo Lorem ipsum dolor sit amet , consectetur adipiscing elit. Nullam tempor vestibulum ex, eget consequat quam pellentesque vel. Etiam congue sed elit nec elementum. Morbi diam metus, rutrum id eleifend ac, porta in lectus. Sed scelerisque a augue et ornare. Donec lacinia nisi nec odio ultricies imperdiet. Morbi a dolor dignissim, tristique enim et, semper lacus. Morbi laoreet sollicitudin justo eget eleifend. Donec felis augue, accumsan in dapibus a, mattis sed ligula. Vestibulum at aliquet erat. Curabitur rhoncus urna vitae quam suscipit , at pulvinar turpis lacinia. Mauris magna sem, dignissim finibus fermentum ac, placerat at ex. Pellentesque aliquet, lorem pulvinar mollis ornare, orci turpis fermentum urna, non ullamcorper ligula enim a ante. Duis dolor est, consectetur ut sapien lacinia, tempor condimentum purus. Obtén acceso completo Accede a todos los puestos de alto nivel y consigue el trabajo de tus sueños. Inscríbete ahora

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