Company Description At TAPI we re not just a company we re a community committed to advancing health from the core As the world s leading supplier of active pharmaceutical ingredients APIs we partner with 80 of the top 50 global pharmaceutical companies With a legacy spanning over 80 years and a portfolio of more than 350 products as well as custom CDMO services we re shaping the future of health worldwide
Our strength lies in our people a team of over 4 200 professionals across 13 state-of-the-art facilities in Italy Hungary the Czech Republic Croatia Israel Mexico and India Together we innovate solve problems and deliver excellence Join us and be part of a mission that transforms lives
Key Responsibilities Review of all documentation i e batch records test results deviation LIR OOS CAPA validation COA Change Controls etc except analytical data related to batch release prior to disposition release or rejection of batch Review of executed document like batch record etc and also to ensure on time compliance of errors deviations identified if any Review of step-by-step performance and compliance to batch manufacturing and packaging record requirements and resolution of any errors deviations identified Monitoring and follow-up of corrective and preventive actions review approval and on time closure of the CAPA in order to resolve an event Review Process documentation i e Protocol report of reviewing effectiveness to determine the effectiveness of a corrective or preventive action Involving in investigation and ensuring on time closure of the investigation and event with resolution including corrective and preventive actions along with effectiveness determination Initiating NTM to Senior Quality Unit Management Operations and other applicable functions for the purpose of expedited communication of critical quality compliance related issues Ensuring Quality interface with internal and external customers when dealing with activities such as issue resolution product info
📌 Quality Analyst (Gajraula)
🏢 Tapi
📍 Gajraula
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