Team Member

**Company Description**
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. 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 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.
**Job Description** Roles & Responsibilities**
- To ensure GLP activity’s in Laboratory and Compliance.
- To ensure safety practices are followed in the Laboratory.
- To ensure analytical record of testing maintained online properly.
- Responsible for review of analytical data includes electronic data related to Raw materials, packing materials, water samples, Audit trail review of respective analytical data through LIMS.
- Release of Quality control materials like Raw material, Packing material, In process, Finish product and stability.
- Responsible for review of Instrument/Equipment’s calibration raw data.
- To ensure Reference standard/impurity standard, working standard, primary standard and all related records are maintained as per the relevant SOPs.
- Investigation and approval of OOS, OOT and incidents.
- Investigation, root cause analysis, Corrective Action and Preventive action for incidents.
- Review and Approval of stability compilation sheet.
- Review and approval of masters in LIMS.
- Audit trail review and verification of Quality control instruments/equipment.
- Looking for compliance in quality control.
- Any other work assigned by Head QA/Designee.

**Qualifications** Educational qualification**:A Bachelor’s degree in Pharmacy, Chemistry.
**Minimum work experience**: 3 to 10 years of experience in pharmaceutical manufacturing or a similar role

**Skills & attributes**:

- Release of Quality control materials like Raw material, Packing material, In process, Finish product and stability.
- Responsible for review of Instrument/Equipment’s calibration raw data.
- To ensure Reference standard/impurity standard, working standard, primary standard and all related records are maintained as per the relevant SOPs.
- Investigation and approval of OOS, OOT and incidents.
- Investigation, root cause analysis, Corrective Action and Preventive action for incidents.

**Additional Information** About the Department**
**Global Manufacturing Organisation (GMO)**
At Dr. Reddy's Laboratories, we are dedicated to making a meaningful impact on global healthcare through precision manufacturing and innovation. With a legacy of excellence, we are a leading force in the pharmaceutical industry.
We operate 19 state-of-the-art manufacturing plants across Hyderabad, Vizag, Baddi, Mexico, Shreveport, and Mirfield, comprising 8 OSD facilities, 3 Injectables facilities, and 8 API facilities.
Benchmarking manufacturing processes and continuous operational excellence are at the core of our capability to deliver quality medicines to our patients in 66 countries. We manufacture a portfolio of complex APIs and 1,150+ drug master files across key therapy areas such as Oncology, Cardio-vascular, Central Nervous System and Anti-Diabetes. he World Economic Forum has recognised our largest manufacturing facility in Bachupally, Hyderabad, as part of its Global Lighthouse Network. We aspire to be the most efficient pharma operations in the world. Our productivity improvement and digitalisation ef