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.



• CSV for assigned projects; responsibilities include but not limited to vendor evaluation, creation of Project Validation Plan based on the criticality of the proposed system, in consensus with the vendor, based on their Quality Systems.
• Perform system risk assessments and review action plans to ensure compliance during and after the system validation.
• Define risk based strategies for the validation of the systems, which includes but not limited to validation methodologies, testing activities, documentation, and version release protocols.
• Develop and review computer system validation deliverables for accuracy, consistency, clarity and completeness.
• Provide training related to computerized systems validation, quality and compliance to users and appropriate personnel.
• Ensure the compliance of computerized systems to regulatory requirements, including but not limited to 21 CFR Part 11 and other applicable regulations.
• Review of change controls with respect to business process, any changes in SAP system. Review of validation deliverables for SAP Change Requests; Establishing and implementing corrective and preventive actions and process improvements initiatives for CSV projects.
• Facing regulatory, customer, IT Quality System related inspections for all computerized systems across the company.
• Review of computerized systems post go-live to ensure compliance with the applicable procedures



Qualifications Educational qualification: A Bachelor's degree in Pharmacy, MSc,Chemistry, MSc Microbiology Chemical Engineering, B.Tech ( Applied Electronics & Instrument) or a related field with experience in CSV



Minimum work experience : 3 to 7 years of experience in pharmaceutical manufacturing or a similar role



Skills & attributes:



Technical Skills

• Knowledge of microbiology and aseptic practices, cleaning validation activities, sampling and relevant standards.
• Proficiency in performing line clearance, material verification, start-up checks, and in-process checks following batch manufacturing and packing records.
• Experience in timely sampling and testing of in-process, reserve, and finished samples, as well as stability samples and environmental monitoring.
• Skilled in reviewing batch manufacturing and batch packing records, ensuring accuracy and certification after execution.




Behavioural Skills

• Attention to detail in performing line clearance, verification, and record reviews.
• Skilled in time management and coordination for sampling, testing, and execution of batch manufacturing and packing activities.
• Communicates effectively with team members and stakeholders regarding batch-related activities and compliance.
• Applies problem-solving skills in addressing issues related to line clearance, sampling, and record certification.
• Demonstrates a focus on maintaining high-quality standards and adhering to regulatory compliances in manufacturing processes.
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 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. 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/#!/