POSITION SUMMARY: Assist in maintaining the quality management system (QMS) for the site to ensure continuation and retention of certification. Performing activities that supports elements if the QMS and support local process owners in ensuring QMS and Regulatory compliance. Report any field actions to the regulatory authority within the stipulated timelines. ESSENTIAL JOB RESPONSIBILITIES: + Update SOPs as and when Needed to ensure applicability + Capture Non-Conformance (NCs) into the eQMS system and ensure continuous trending of NCs and their causes (Act as the region’s NC coordinator) + Facilitate and co-chair CAPA board meetings + Conduct internal Audits + Training associates on QMS tools + Manage Compliance training for regional associates + Conduct ERP system quality releases of goods + Report on the Monthly quality KPIs for the site and region Drive the on time delivery of quality objectives & report for the site and region in collaboration with process owners + Support the continued effectiveness of the QMS MINIMUM REQUIREMENTS: Education and Experience (in years): + At least three years experience in Quality Assurance, in the medical diagnostics I pharmaceutical industry or relevant quality assurance qualification + Any Life Science Degree, Quality Degree or Operations degree Knowledge and skills: + ISO 13485 (2016) + Basic Knowledge of Local applicable regulatory requirements + Excellent writing and Verbal Skills (English required) + Good computer Skills (i.e., MS Office 365, Windows) Other: + High adaptability and flexibility + Multi-tasking ability + Pay Attention to detail + Precision in writing (Good English grammar) + Collaborative (Work well with other teams) + Careful and thorough Key relationships + Maintain good coordination and team work with management and associates of all functional departments for the Site (Customer Services, Filed Application, Technical Support, Service Coordination’s , Logistics, HR, Medical Affairs, Sales + Liaise with Associates from other Sites in different countries TRAINING RESPONSIBILITIES: (REQUIRED) + Complete all assigned and required training satisfactorily and on time Physical requirements/abilities: + Must have good eyesight + Will be required to work after hours as needed. N/A At Danaher we bring together science, technology and operational capabilities to accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. Our global teams are pioneering what’s next across Life Sciences, Diagnostics, Biotechnology and beyond. For more information, visit www.danaher.com. At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.