GSK Consumer - LOC Quality Specialist (contract)

Nombre del sítio: Korea - Seoul Fecha de publicación: Jun 26 2022 As a LOC Quality Specialist, you will be responsible for providing effective and efficient support to the Local Operating Country (LOC) Quality Manager to maintain effective Quality Management System (QMS) and perform LOC Quality Operation activities in compliance with GSK Policies, QMS and local regulations. This position is 1 year contract based position and it will be extended for another year based on the performance. Key Responsibilities Execute and deliver Local Operating Country (LOC) Quality Objectives and LOC Quality Improvement Plan. Perform trending of Quality KPIs to support continuous improvement at the LOC. Maintain a robust, sustainable and effective QMS (Quality Management System) at the LOC to ensure LOC Quality operations and processes are in full compliance with GSK standards and policies, Good Manufacturing Practices (GMP), Good Documentation Practices (GDP) and local regulatory requirements. Responsible for quality performance of the assigned 3rd party contractors/ service providers/ suppliers and ensuring potential quality and compliance issues are identified, communicated and promptly resolved. Ensure quality systems are in place and in use according to GSK QMS standard. Coordinate LOC Quality Council meetings. Participate in LOC Quality Council(s) in identifying Quality related issues and continuous improvement Opportunities. Perform activities to support risk management process to ensure timely mitigation of quality risks. Perform quality impact assessment to ensure all planned changes at the LOC are appropriately managed and are appropriately managed through change control. Perform self-inspections at the LOC and 3rd party service providers’ operations with potential product quality and regulatory compliance impact. Support investigations and root cause analysis in response to deviations, quality issues, audit findings and customer complaints. Ensure product supplied to market have the right quality, safety, efficacy and comply with local regulations. Why you? Basic Qualifications: We are looking for professionals with these required skills to achieve our goals: 5+ years of experience in life sciences industry in Quality Assurance role Experience with cGMP (Clinical Good Manufacturing Practices) in pharma testing/secondary repacking Operational experience with Good Documentation Practices (GDP) in warehousing and distribution *LI-GSK Why GSK? Our values and expectations are at the heart of everything we do and form an important part of our culture. These include Patient focus, Transparency, Respect, Integrity along with Courage, Accountability, Development, and Teamwork. As GSK focuses on our values and expectations and a culture of innovation, performance, and trust, the successful candidate will demonstrate the following capabilities: Operating at pace and agile decision-making – using evidence and applying judgement to balance pace, rigour and risk. Committed to delivering high quality results, overcoming challenges, focusing on what matters, execution. Continuously looking for opportunities to learn, build skills and share learning. Sustaining energy and well-being. Building strong relationships and collaboration, honest and open conversations. Budgeting and cost-consciousness. *This is a job description to aide in the job posting, but does not include all job evaluation details. Nuestro objetivo es ser una de las empresas de atención médica más innovadoras, de mejor desempeño y más confiables del mundo. Creemos que todos aportamos algo único a GSK y cuando combinamos nuestros conocimientos, experiencias y estilos, el impacto es increíble. Únase a nuestra aventura en GSK donde se inspirará para hacer el mejor trabajo para nuestros pacientes y clientes. Un lugar donde puede ser usted mismo, sentirse bien y seguir creciendo. Aviso importante a las empresas o agencias de empleo GSK no acepta recomendaciones de empresas de empleo o agencias de empleo con respecto a las vacantes publicadas en este sitio. Todas las empresas o agencias de empleo están obligadas a ponerse en contacto con el Departamento de Contrataciones Comerciales y Generales o el Departamento de Recursos Humanos de GSK para obtener autorización previa por escrito antes de recomendar a cualquier candidato a GSK. La obtención de autorización previa por escrito es una condición precedente a cualquier acuerdo (verbal o escrito) entre la empresa o agencia de empleo y GSK. En ausencia de dicha autorización por escrito, se considerará que las acciones que emprenda la empresa o agencia de empleo se han realizado sin el consentimiento o el acuerdo contractual de GSK. Por lo tanto, GSK no será responsable de ninguna tarifa derivada de tales acciones o cualquier tarifa que surja de cualquier recomendación por parte de las empresas o agencias de empleo con respecto a las vacantes publicadas en este sitio.