Team Member - QC

Dr. Reddy's Laboratories; Visakhapatnam; On-site; INR 1,500,000 - 1,900,000; Full time

Benefits offered by this job

Joining & relocation support

Family support (Maternity & Paternity)

Learning and development opportunities

Medical coverage for yourself and your

Life coverage for yourself

Job summary

Dr. Reddy’s Laboratories is seeking a senior QC professional for stability and analytical operations at Vizag. The role covers GMP/GLP/GDP adherence, sample handling, stability data management, and CAPA closures within the GMO Quality group.

You will ensure instrument calibration, execute stability tests, manage master schedules, and drive investigations for out-of-spec events, contributing to regulatory-ready documentation.

Qualifications

• Educational qualification: B.Sc/ M.Sc/ B.Pharma.
• Minimum work experience: 9 to 11 years

Responsibilities

• 1.1 Responsible for Entry and Exit procedures in QC-Department.
• 1.2 Responsible for GMP / GLP/ GDP and safety Compliance.
• 1.3 Ensuring and maintaining good housekeeping in the lab.
• 1.4 To ensure proper Handovering of the shift.
• 1.5 Stability protocol preparation, stability analysis and execution
• 1.6 Handling of stability chambers and maintenance.
• 1.7 Stability data sheet preparation and compilation
• 1.8 Daily chamber reports print taking & review.
• 1.9 Preparation of monthly & yearly master schedule for stability.
• 1.10 Responsible for loading and withdrawal of stability samples for intermediate & API.
• 1.11 Analysis of Inprocess, RM, PM, Intermediates, API, working standard qualifications and stability samples, Experimental samples from Process R&D & Method transfer.
• 1.12 Preparation and Review of QC related protocols and batch related protocols.
• 1.13 Analysis of Raw materials, In process, Intermediates, API, working standard qualifications and stability samples and Calibration of HPLC
• 1.14 To operate the instruments of their respective SOP’S.
• 1.15 To ensure whether the instrument is calibrated or not before start of the analysis.
• 1.16 To carry out the analytical tests as per the related SPEC and MOA’S.
• 1.17 Handling of incidents, OOS and OOT.
• 1.18 Carrying out investigations and preparation of investigation reports and impact assessment.
• 1.19 Ensuring the sampling from the analyst and weighing procedure for sampling.
• 1.20 Issuing the Work order & Breakdown for necessary works in QC lab.
• 1.21 Intimation to engineering team regarding Work orders in QC.
• 1.22 Responsible for handling of documents and Waste labels in Drop box.
• 1.23 Responsible for CAPA closure.
• 1.24 Handling of materials through isolator in HPAI QC.
• 1.25 To undergo the training assigned in LMS.
• 1.26 COA Preparations for Dispatch Purpose& typical COA preparation for Regulatory Affairs submission.
• 1.27 Responsible for CCF initiation and action plans closure.

Education

B.Sc/ M.Sc/ B.Pharma

Job description

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.

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Job Description

• 1.1 Responsible for Entry and Exit procedures in QC-Department.
• 1.2 Responsible for GMP / GLP/ GDP and safety Compliance.
• 1.3 Ensuring and maintaining good housekeeping in the lab.
• 1.4 To ensure proper Handovering of the shift.
• 1.5 Stability protocol preparation, stability analysis and execution
• 1.6 Handling of stability chambers and maintenance.
• 1.7 Stability data sheet preparation and compilation
• 1.8 Daily chamber reports print taking & review.
• 1.9 Preparation of monthly & yearly master schedule for stability.
• 1.10 Responsible for loading and withdrawal of stability samples for intermediate & API.
• 1.11 Analysis of Inprocess, RM, PM, Intermediates, API, working standard qualifications and stability samples, Experimental samples from Process R&D& Method transfer.
• 1.12 Preparation and Review of QC related protocols and batch related protocols.
• 1.13 Analysis of Raw materials, In process, Intermediates, API, working standard qualifications and stability samples and Calibration of HPLC
• 1.14 To operate the instruments of their respective SOP’S.
• 1.15 To ensure whether the instrument is calibrated or not before start of the analysis.
• 1.16 To carry out the analytical tests as per the related SPEC and MOA’S.
• 1.17 Handling of incidents, OOS and OOT.
• 1.18 Carrying out investigations and preparation of investigation reports and impact assessment.
• 1.19 Ensuring the sampling from the analyst and weighing procedure for sampling.
• 1.20 Issuing the Work order & Breakdown for necessary works in QC lab.
• 1.21 Intimation to engineering team regarding Work orders in QC.
• 1.22 Responsible for handling of documents and Waste labels in Drop box.
• 1.23 Responsible for CAPA closure.
• 1.24 Handling of materials through isolator in HPAI QC.
• 1.25 To undergo the training assigned in LMS.
• 1.26 COA Preparations for Dispatch Purpose& typical COA preparation for Regulatory Affairs submission.
• 1.27 Responsible for CCF initiation and action plans closure.

Qualifications

• Educational qualification: B.Sc/ M.Sc/ B.Pharma.
• Minimum work experience: 9 to 11 years

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. the 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 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
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/#!/

Job Family

• Job Family: Quality
• Sub Job Family: Quality Control
• Preferred type of working: On-Premise
• Business unit: GMO