GSK Consumer - LOC Quality Specialist (contract)

Nom du site: Korea - Seoul Date de publication: 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. Our goal is to be one of the world’s most innovative, best performing and trusted healthcare companies. We believe that we all bring something unique to GSK and when we combine our knowledge, experiences and styles together, the impact is incredible. Come join our adventure at GSK where you will be inspired to do your best work for our patients and consumers. A place where you can be you, feel good and keep growing. Important notice to Employment businesses/ Agencies GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.