Job Summary:

The candidate should have the skill to perform the IPQA rounds performing the procedure Vs practice gap identification conducting the line clearance activities participate in Intermediate sampling BPR/ECR review and identifying the gaps in documents and archival management.

Roles & Responsibilities

- You will be responsible for executing or assigning IPQA activities during shifts conducting line clearances material verification and coordinating sampling activities to ensure product quality and compliance.
- Your tasks also involve reviewing the records maintained by the Production teamWarehouse and ESDR&D; conducting all documentation with respect to Quality Assurance (QA) activities ensuring that documentation is happening online and follow the deviation reporting system in the case of deviations.
- Witenssing the intermediate sampling rinse and swab sampling activities.
- Review of the BPRs/ECRs/ACRs within the TAT timelines and timely updation of review findings and closure of the observation by coordinating the CFT.
- Conducting the IPQA rounds as per the schedule and updation and closure of the observations.
- Management of the Doc cell activities like issuance retrieval obsoletion and destruction after the retention period inline to document life cycle management SOP.
- You will be responsible for issuance availability and adherence of approved procedures to the manufacturing team.
- Your responsibilities also include verifying whether the manufacturing facility meets basic Positive Manufacturing Practice (GMP) requirements at all times including facility upkeep environmental conditions segregation of materials and status case of deviations you will follow the incident management process.




- You will provide essential support to investigations related to Out-of-Specification/Out-of-Trend (OOS/OOT) results deviations etc. by collating data and conducting interviews.

Qualifications :

Educational qualification: in Chemistry.

Minimum work experience: 3 to 12 years of experience in pharmaceutical manufacturing or a similar role

Additional Information :

About the Department
Global Manufacturing Organisation (GMO)
At Dr. Reddys 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 1150 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 productive pharma operations in the world. Our productivity improvement and digitalisation efforts are key to staying competitive meeting business imperatives and meeting our ambitious ESG goals. Building such factories of the future is integral to innovation and to build healthcare of the future.

Benefits Offered
At Dr. Reddys we actively help to catalyse your career growth and professional development through personalised learning programs.
The benefits you will enjoy at Dr. Reddys 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. Reddys why they come to work every day and theyll say because Good Health Cant 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 were always attuned to the current 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

Remote Work :

No

Employment Type :

Full-time

📌 Team Member – Quality Assurance (IPQA) (Visakhapatnam)
🏢 Dr. Reddy's Laboratories
📍 Visakhapatnam