About the role the quality management system is a crucial component of our organization, ensuring compliance with regulatory standards and global quality guidelines. as a key member of our team, you will support the qa manager in executing and improving the system, aligned with gmp, gdp, and local regulations. responsibilities: - manage complaints, deviations, and change controls to maintain regulatory compliance. - spearhead medical device inspections to ensure adherence to industry standards. - collaborate with the qa manager to implement and refine quality management processes. requirements: - demonstrate intermediate-high english proficiency for effective global communication. - possess a degree in pharmaceutical chemistry or a related field. - hold current registration and professional license with invima. - showcase experience in the pharmaceutical industry, specifically in quality, product release, pharmacovigilance, and gmp/gdp compliance. - familiarize yourself with relevant regulations, such as resolution 4816 of 2008 (pharmacovigilance). desirable skills: - pursue training as an internal auditor to enhance your skillset. - demonstrate expertise with systems like trackwise, sap (le/wm), mango, excel, and sharepoint. - cultivate knowledge of validation processes, document management, and activities related to product release and transportation....
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