Responsible for Review of Quality Control documents and Electronic data.
•Responsible for initiation, review and investigation related to Deviations, OOS, OOAL, CAPA & LIR.
•Responsible for Review of documents related to GLP, Raw material, Packaging material, Inprocess, Finished, Stability and Miscellaneous.
•Responsible for preparation and review of Quality control SOP, GTP, STP and Specifications.
•Responsible for maintaining of Good laboratory practices in the lab.
•Responsible for maintain of regular cleanliness of laboratory.
•Responsible for overall management of Laboratory compliance.
•Responsible for Review of Volumetric solutions, Limit Test solutions, Test solutions, LNBs, CoA's and all other test reports.
•Responsible for Review of calibration reports of Instruments and Equipments as and when required.
•Responsible for initiating and review of Change controls and Deviations.
•Responsible for review and preparation of Method verification Reports/Protocols.
•Responsible for review of Method verification activities.
•Responsible for checking the maintenance of Columns, reference standards and Working standards.
Qualification - B.Pharmacy, M.Pharmacy
Amneal is an equal opportunity employer. We do not discriminate based on caste, religion, gender, disability, or any other legally protected status. We believe in fostering a workplace that values diversity and inclusion.
Amneal (NASDAQ: AMRX) is rapidly becoming one of the most dynamic, purpose-driven pharmaceutical companies delivering more affordable access to essential medicines. Our family delivers for yours through a robust U.S. generics business, a growing branded business and deepening portfolios in injectables, biosimilars and select international markets. We’ve bolstered our world-class scientific rigor, production capabilities and commercial infrastructure. And we invest substantially in our people through leadership development and employee well-being programs – all so we can deliver even more value. We are Amneal and We make healthy possible.
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