2.0 - 6.0 years

0 Lacs

vadodara, gujarat

On-site

You will be responsible for the inspection of received routine samples and their distribution to various sections of the laboratory based on the type of analysis. It is crucial to communicate any abnormal samples or non-receipt of routine samples to the shift in charge in a timely manner. Adherence to standard test methods, work instructions, and compliance with Quality system procedures are essential for ensuring accurate test results. You will conduct required tests and validate the results before reporting to maintain result reliability. In case of exceptions or deviations in test results, you must promptly highlight and report them to the relevant personnel. During emergency situations, you will perform on-spot mitigation under the guidance of the shift in charge. Effective sample management, including safe disposal of leftover samples, is a key aspect of the role. Timely entry of test results in the Laboratory Information Management System (LIMS) is vital for smooth operations. Furthermore, it is important to ensure the availability of analytical equipment by cleaning and maintaining them for subsequent experiments or tests. Maintaining good housekeeping in the laboratory and proper data management through accurate recording of results in various registers are essential responsibilities. Compliance with Health, Safety, Environment, and Facility (HSEF) procedures and regulations, as well as reporting unsafe acts or conditions, are paramount for ensuring a safe working environment. Continuous learning and self-initiative for training to enhance competencies, as well as participation in external training as advised, are encouraged. Specific competencies include timely execution of tasks, handling erratic changes in plans, effective sample management, identifying exceptions in test results, prioritizing activities, and complying with HSEF regulations. The ideal candidate should have a B.Sc. in Chemistry or a Diploma in Chemical Engineering, along with preferably 2 years of experience in QA/QC discipline. Relevant knowledge of test procedures, sample handling, analysis, and effective communication with shift in-charge are key skills required for this role.,

Posted 3 weeks ago

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Sr. Officer- Quality Control SUN PHARMA

2.0 - 6.0 years

0 Lacs

bihar

On-site

Responsibility for conducting Chemical/Instrumental testing of raw material samples to ensure quality standards are met for products manufactured at Sun Pharmaceutical Industries Ltd, both for the domestic market and export to emerging markets. This includes analyzing and reporting stability and finished goods samples, monitoring gowning and sanitation practices, and ensuring compliance with standard operating procedures for analytical instruments. Responsible for system upgrades in alignment with Corporate Quality (CQ) and regulatory guidelines, operating analytical equipment in quality control during assigned shifts, and maintaining accurate documentation and record-keeping practices following Good Documentation Practices (GDP) and laboratory protocols. Supporting internal audits, regulatory inspections, and FDA audits by adhering to best practices and following all cGMP regulations as per Schedule M. Ensuring safety procedures are followed when handling analytical equipment and hazardous materials, completing assigned trainings to address identified training needs, and calibrating analytical equipment as per calibration procedures. Maintaining analytical equipment and laboratories in optimal working condition, overseeing stock levels of working standards, columns, reagents, chemicals, and glassware, and following procedures for non-conforming results as outlined in Standard Operating Procedures (SOPs) related to Out-of-Trend (OOT), Laboratory Incidents, and Out-of-Specification (OOS) results. Adhering to administrative procedures regarding attendance, leave, and other benefits in compliance with company policies and regulations.,

Posted 1 month ago

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Officer-Quality Control SUN PHARMA

3.0 - 7.0 years

0 Lacs

bihar

On-site

Responsibility for conducting Chemical and Instrumental testing on samples of raw materials. Ensuring the quality of products manufactured by Sun Pharmaceutical Industries Ltd for both domestic and emerging markets. Implementing system upgrades in alignment with CQ and regulatory guidelines. Analyzing and reporting stability and finished goods samples when necessary. Monitoring gowning and sanitation practices within the operational area. Ensuring compliance with standard operating procedures for analytical instrument operation. Operating analytical equipment in quality control as per assigned shifts. Adhering to good documentation procedures and recording results as per SOP on GDP and laboratory practices. Supporting internal audits, regulatory inspections, and FDA audits with best practices. Adhering to cGMP regulations as per schedule M. Maintaining safety protocols for handling analytical equipment and potential hazards. Completing assigned training as per identified training needs through organized sessions or self-study. Calibrating analytical equipment as per calibration procedures for assigned responsibilities. Keeping analytical equipment and laboratories in good operational condition. Managing stock levels of working standards, columns, reagents, chemicals, glassware, etc. Following procedures for non-conforming results as outlined in SOPs for OOT, Lab Incidents, and OOS. Complying with administrative procedures related to attendance, leave, and other benefits.,

Posted 1 month ago

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