![Dr. Reddy's Laboratories](https://media.trabajo.org/img/noimg.jpg)
Team member- Engineering Assurance
4 weeks ago
Dr. 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. Asthepharmaceutical industry evolves and undergoes disruption, we see an opportunity –tostrengthen our core further (the next steps) and to build the future (the new bets).
‘TheNextand 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 transparency
Dr 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.
- Validation Master Plan (VMP) preparation, review, approval & monitoring and updation
- Equipment Qualification Protocol & Report Review & Approval.
- Water System Qualification (Potable & Purified), regular monitoring and trend updating.
- Utilities Qualification and periodical performance monitoring.
- HVAC Qualification and periodical performance monitoring and Review of PeriodicalEnvironmental Monitoring.
- Review and Approval of Calibration and Preventive Maintenance.
- Ensuring timely and error free GXP review of computerized systems qualification & validation as per IT compliance.
- Verification of computerized systems Audit trail of GxP Applications.
- Review & Approval of IT schedule activities & ensure of completeness of periodic scheduled activities.
- Review and Approval of Quality Risk management
Educational qualification: B. E/ B. Tech (Preferred is B.E Mechanical/ Electrical/ Instruments/Chemical) with AutoCAD
Minimum work experience : 7-10 years of experience in the pharmaceutical industry, with a focus on quality management and Engineering assurance.
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