Job Summary
We are looking for an individual  who can  conduct thorough equipment qualification, ensuring adherence to regulatory standards and product specifications. Your role involves maintaining accurate records, troubleshooting and supporting laboratory equipment and instrument qualification and routine calibrations, contributing to the quality and compliance of laboratory operations.

Roles & Responsibilities
• Candidate shall be responsible for Conducting Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) for all laboratory equipment’s and instruments.

• Candidate should have the knowledge on microbiology techniques and should be capable of writing the URS and relevant protocols to ensure equipment complies with regulatory standards and Good Manufacturing Practices.

• Candidate shall  be responsible for maintaining accurate and detailed records of test results, including documentation of all testing procedures, observations, and data analysis.
• Candidate shall  operate and maintain laboratory equipment and instrumentation, ensuring proper calibration and performance verification.
• Candidate shall be responsible for adhering to Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP), and other regulatory guidelines during all laboratory activities.
• Candidate shall have experience on handling and writing investigations/Deviations and OOS reports.

Candidate should be qualified as M.Sc Microbiology

About the Department
Biologics
Currently operates in the Global Biosimilars business - a segment that is poised for attractive and sustained growth over the next 10–15-year time horizon.
With a robust portfolio of biosimilar products across key therapeutic areas, covering ~US$80+ Bn in innovator sales – future business pipeline covers a variety of product classes and therapy areas, and new modalities. Fully integrated organization with over two decades of experience in developing, manufacturing and commercializing multiple biosimilar products.
With a Product Development engine that has end-to-end capabilities – in-house clone development, upstream and downstream process development, bioanalytical development and proprietary formulation.
Supported by a Clinical and Regulatory team with experience in executing complex biosimilar programs with innovative global trial designs.
We have a proven experience in commercial-scale manufacturing across a variety of technology platforms with global quality standards and a highly competitive cost structure
Rich experience of commercializing high-quality biosimilars in multiple markets with over 900,000 patients having benefited from our products till date.

Benefits Offered
At Dr. Reddy’s we actively help to catalyse your career growth and professional development through personalised learning programs.
The benefits you will enjoy at Dr. Reddy’s are on par with the best industry standards. They include, among other things and other essential equipment, joining & relocation support, family support (Maternity & Paternity benefits), learning and development opportunities, medical coverage for yourself and your family, life coverage for yourself.

Our Work Culture
Ask any employee at Dr. Reddy’s why they come to work every day and they’ll say, because Good Health Can’t Wait. This is our credo as well as the guiding principle behind all our actions. We see healthcare solutions not only as scientific formulations, but as a means to help patients lead healthier lives, and we’re always attuned to the new and the next to empower people to stay fit. And to do this, we foster a culture of empathy and dynamism. People are at the core of our journey over the last few decades. They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success. We believe that when people with diverse skills are bound together by a common purpose and value system, they can make magic.
For more details, please visit our career website at https://careers.drreddys.com/#!/