Technician- Pilot Plant

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.

1. 1. Ready to work on anti-cancer and potent product manufacturing.
   2. Experience in closed loop transfer production line is preferrable.
   3. Acceptance to work in small volume facility.
   4. Responsible for machine setting, operation and cleaning of machines as per the operating instructions and standard operating procedures.
   5. Responsible to meet the pilot production schedule and adherence to the delivery timeline.
   6. Execution of pilot-bio/ clinical trial/ trial batches as per manufacturing instructions.
   7. Responsible to record process parameters during batches manufacturing, online documentation, logbooks and status labeling.
   8. Adherence to quality, safety procedures & policies at manufacturing sites.
   9. Responsible for calibration of the instruments as per the schedule and applicable procedure.
   10. Responsible for carrying out the in-process checks as per the instructions in the batch production record.
   11. Responsible for upkeep of the pilot production area.
   12. Responsible for strict adherence to cGMP requirements and compliance to regulatory requirements.
   13. Responsible to follow practices as per relevant SOPs.
   14. To support qualification of equipment and instruments and release for regular usage.
   15. Responsible for line clearance procedure of equipment and area.
   16. To follow personal hygiene, safety requirements and discipline on the shop floor.
   17. To follow applicable, SHE procedures at workplace.
   18. Ready to work in oncology & non-oncology formulation oral solid dosage forms.
       

Qualifications

ITI/ diploma/BE in any discipline with 6-10 years of experience in Oral Solid dosage forms in pharmaceutical industry.

Additional Information

About the Department

Integrated Product Development Organisation

Benefits Offered