Title: Senior Officer
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Job Title: |
Sr Officer -Lab QA |
Business Unit: |
Global Quality And Compliance |
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Job Grade |
G12B |
Location : |
Gangtok |
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At Sun Pharma, we commit to helping you “Create your own sunshine”— by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine?
As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.” Key responsibilities: To monitor all activities in QC department as per GLP. To ensure the proper closing of OOS, Lab events, OOC & OOT, Batch Rejection (RM, PM, FP & Stability) on time. To review the OOS, Lab event, OOC, OOT, Non- conformance and ensure that the defined procedure as followed by QC to identify the root cause and establishment of CAPA. To review the Log books/ Formats, Electronic & Paper raw data generated in QC lab as a secondary check by QA reviewer. To Prepare, review of trend of all laboratory errors and effective CAPA implementation to reduce laboratory errors. To monitor completion of Analyst Qualification prior to assign work to analyst. Periodic review of Data Integrity and shop floor inspection of Lab as per predefined procedure. To review the Reduce Testing protocol as per SOP and implement. Responsible for all aspects of quality assurance in quality control laboratories w.r.t. to assessment of quality issues in lab , review of documentation, compliance in QC labs, QC lab readiness for inspection, and contract testing lab management at the Site per current Good Manufacturing Practices requirements To maintain proper online implementation of SOPs/ CAPA and Preventive Maintenance through proper training To ensure compliance of the functional area with company Health and Safety Policies. To ensure people development initiatives and training are implemented within QA To participate in Computer System Validation To ensure the completion of individual training requirements with in timeline. To ensure the audit compliance. To ensure the preparation of Monthly data for laboratory error for CQA Reporting. Any other work assigned by HOD |
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Travel Estimate |
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Job Requirements |
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Educational Qualification |
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Experience |
Tenure: 3 to 5Yrs |
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Your Success Matters to Us At Sun Pharma, your success and well-being are our top priorities! We provide robust benefits and opportunities to foster personal and professional growth. Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. Let’s create a brighter future together! |
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Disclaimer: The preceding job description has been designed to indicate the general nature and level of work performed by employee within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent(s). |
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