Aurolife was founded in 2008 as part of a group of companies that has a long history of excelling in generic pharmaceutical prouct development and manufacturing. Aurolife has a 10 year history of extraordinary manufacturing practices in the solid oral dose arena. The support and expertise of our parent organization has given Aurolife a jump start in building a solid pharmaceutical portfolio very quickly. The Aurolife family consists of an experienced management team with expertise in manufacturing, R&D, Quality Assurance and Quality control and regulatory affairs. In addition to several formulations under manufacture, we have a robust pipeline of products. Aurolife's aim is to provide healthcare at economical prices to make this a healthier world to live in.
Supervisor is to monitor all IPQA activities for all shifts if needed. Manage the scheduling for all IPQA.
Manage the syllabuses and training for all of IPQA. Help support the manager with all deviations, incidents, CAPA’s, change controls for the IPQA and manufacturing floor. Be the backup and support batch record review and release activities when needed.