8 Deviation Reporting Jobs

Role Overview: As an Associate Manager in the Quality Control department at ZLL-SEZ Oncology Injectable, your role is critical and involves planning routine activities, reviewing analytical raw data for accuracy, reporting discrepancies, performing stability analysis, managing key elements of the Quality management system, ensuring timely sampling and testing of materials, coordinating with internal and external teams, and maintaining laboratory resources and equipment. Key Responsibilities: - Plan routine activities of the respective section - Review all analytical raw data, calibration reports, and trend data for accuracy - Report any discrepancies and follow deviation reporting procedures...

Biocon Biologics is a subsidiary of Biocon Ltd, an innovation led global biopharmaceuticals company, engaged in developing high quality, affordable biosimilars to expand access to cutting-edge therapies globally. As a fully integrated pure play biosimilars organization, Biocon Biologics aspires to transform patient lives through innovative healthcare solutions. With a large portfolio of biosimilars under global clinical development and multiple commercialized products in developed markets, Biocon Biologics believes in the power of strong partnerships to co-create the future of healthcare and positively impact millions of lives. Key Responsibilities: - Adherence to cGMP, cGLP, and GDP standar...

As the Block Head / Production Manager at Ankleshwar Unit 2, your key role involves overseeing the production planning and execution process. Your responsibilities include: - Managing the plant manpower according to production planning - Handling raw material management in alignment with production planning - Coordinating with cross-functional departments for production requirements - Ensuring documents are prepared and reviewed, and approved by QA for production of intermediates or API - Ensuring department procedures comply with system SOPs and departmental SOPs - Reviewing and ensuring completion of production batch records - Reporting and evaluating production deviations and incidents, i...

As a Production Head with 15 to 19 years of experience in pharma API pharma at Sandhurst Road Mumbai, your responsibilities include: - Reviewing, approving, and distributing work instructions for manufacturing activities. - Carrying out production activities as per the production plan. - Deciding on new batch production and monitoring batch processes. - Qualification of production equipment and participation in validation activities. - Checking the quality system in the production department. - Preparing equipment master lists and equipment qualification plans. - Reviewing MFRs, BMRs, BPRs, SOPs, and formats. - Ensuring that all production deviations are reported, evaluated, and investigated...

As an Associate Manager in the Quality Control Department at ZLL-SEZ Oncology Injectable (Alidac), your role is critical and involves the following key responsibilities: - Plan routine activities of the respective section. - Review all analytical raw data and associated documents for accuracy, including calibration/qualification reports, trend data analysis, and quality control testing protocols. - Report and follow up on any discrepancies noticed during the review process, including deviations and incidents. Perform predictive stability analysis on generated data for stability studies. - Log change controls and ensure proper execution following SOPs. Evaluate proposed changes for impact on ...

As a Production Operator in the Plant, your role involves performing production activities in shifts. You will be responsible for operating process sequences through computer systems / HMI and communicating effectively with supporting departments such as QA, QC, warehouse, Engineering, and safety. Your coordination with DCS operators is crucial for the smooth functioning of operations. Key Responsibilities: - Perform activities as per Standard Operating Procedures (SOPs). - Fill Batch Production and Usage log book online. - Carry out all production activities in compliance with current Good Manufacturing Practices (cGMP) norms. - Prepare SOPs, Master Production Batch Records (MPBR) / Batch P...

As the Production Head, you will be responsible for overseeing the manufacturing activities in the pharma API industry. With 15 to 19 years of experience, you will be based at the Sandhurst Road Mumbai head office with a salary of 15 lpa. Your key responsibilities will include reviewing, approving, and distributing work instructions for manufacturing activities. You will ensure the production activities align with the production plan and make decisions regarding new batch production. Monitoring batch processes and reviewing online documentation such as BMR, BPRs, logbooks, and daily records will also be part of your role. Furthermore, you will be in charge of qualifying production equipment,...

The core responsibilities of this role include conducting quality control testing on poultry feed by performing routine chemical and physical tests on raw materials and finished products to assess various parameters such as moisture, protein, fat, fiber, ash, and pH. You will also be responsible for collecting, preparing, and analyzing samples of feed and other materials, as well as recording test results accurately, updating lab records, and generating reports. Operating and maintaining laboratory equipment, including calibration and routine maintenance, is also a key aspect of this position. It is essential to ensure that all testing procedures adhere to Standard Operating Procedures (SOPs...