Company DescriptionDr. Reddy's Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because Good Health Can\'t Wait.We started in 1984 with a modest investment, 20 employees and a bold vision. Today, we have research and development centres, manufacturing facilities or a commercial presence in 66 countries.For nearly four decades, we have stood for access, affordability and innovation based on the bedrock of deep science, progressive people practices and robust corporate governance. As the pharmaceutical industry evolves and undergoes disruption, we see an opportunity - to strengthen our core further (the next steps) and to build the future (the new bets).\'The Next and the New\' is how we aim to continue to be the partner of choice - purpose-driven, future-ready and sustainable. Our aim is to reach over 1.5 Bn+ patients across the world by 2030 by growing our core businesses and building for the future with sustainability at the core of our purpose and strategy. Sustainability for us means operating in a manner that respects people, planet and purpose - helping us conserve precious resources, serve our patients, create value for stakeholders, give back to society, fulfil our potential and maintain our integrity and transparencyDr Reddy's maintains a work environment, free from discrimination and is an equal opportunity employer. We are committed to employ & nurture all qualified diverse workforce without regard to race, colour religion, nationality, sex, age, disability status, genetics, sexual orientation, gender expression, citizenship or any other characteristic or classification protected by applicable law(s) of the country we operate in. We treasure every talent, and recognize merit and diversity in our organization.1.To perform/ensure activities (Operation, cleaning, monitoring and maintenance) for General injectable areas/ \\Visual Inspection and Packing activites/ Accessories/ Instruments associated with Manufacturing and related documents by manually or MES/PAS X.2.To ensure and adhere Organization Safety/Quality policies, Procedures, norms and its effective implementation from time to time.3. Ensure the adherence of SHE standards and policies across the plant with respect to MSI.4. To follow the personnel hygiene practices and discipline.5. To coordinate with the superiors and other related departments for the smooth functioning.6. To ensure the availability of man, machine and material to achieve the production plan.7. Maintaining cGMP practices in production area and report any discrepancies/incidents to immediate supervisor.8. Execution of Qualifications/Validations and manufacturing of Batches.9. To prepare/review and execute GMP documents like SOP, BMR, Investigation report, risk assessment report, URS, qualification, validation, log books/PAS X, study protocols and reports etc. as per Good Documentation Practice.10. Issuance, Receipt and submission of the BMR, BPR, log-books and other GMP records.11. To raise the breakdown requests in SAP and inform to all concerned person.12. To raise analysis requests and coordinate with QC for test results.13. To ensure training completion as per the matrix and to train the production personnel on their routine work.14. To perform any other tasks/projects assigned by Head Operations.15. To perform preventive maintenance activity.QualificationsEducational qualification: A Diploma/B.Sc./B Pharm/B. TechMinimum work experience: 3 to 10 years of experienceSkills & attributes:Technical Skills
Packing line operationsManual and automatic Visual Inspection operations
Behavioural skills
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