Trikona Pharmaceuticals is a biopharmaceutical company focused on developing innovative therapies for unmet medical needs in the areas of oncology and autoimmune diseases.
Hyderabad
INR 2.0 - 3.5 Lacs P.A.
Work from Office
Full Time
coordinate with R&D & production and relevant teams to develop and maintain production schedules Monitor inventory levels and ensure timely replenishment of materials Monitor and manage the progress of the projects closely in coordination with cross-functional departments Analyze production data to identify areas for improvement and efficiency Collaborate with purchasing department to ensure timely delivery of materials Generate reports on production performance and inventory level Participate in cross-functional meetings to discuss production planning and scheduling Assist in the development of production forecasts and capacity planning Optimize Production schedules and managing Inventory levels to ensure efficient operations Implement and maintain production planning systems and tools Support continuous improvement initiatives to optimize production processes and reduce costs
Hyderabad
INR 2.5 - 4.0 Lacs P.A.
Work from Office
Full Time
Handling, storage and retrieval of all the documents pertaining to facility on operation of the functional departments. Deploying Good Documentation Practices throughout all the functions. Allotment of reference numbers, Formatting, distribution, control, revision, retrieval and storage of all master documents. Maintaining of master list of documents. Maintaining online documentation. Issuance of Formats, LNBs & Log books to all departments. Preparation of QA&RA SOPs. Monitoring of Instruments and Equipment calibrations. To involve internal quality and regulatory compliance audits across all the functions. Handling of Training Records across all the functional departments. Monitoring for compliance across all functional departments. Providing adequate support to R&D teams to execute the required documents for regulatory submissions. Review of all quality documents which includes SOPs, Formats, Equipment/Instrument qualifications/ calibrations , drug excipient compatibility studies, API characterization, API solubility studies, Stability studies, Stress studies, Other studies, Method development reports, Specifications, STPs, MFR, method validations, Method transfers, PDR etc. Reviewing of LNBs, Raw data & Log books for data integrity issues.
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