MES Specialist - Drug Product/ Sterile Operations at Dr Reddy's Laboratories Limited

Hyderabad, Telangana, India -

Full Time

Start Date

Immediate

Expiry Date

17 Sep, 26

Salary

0.0

Posted On

19 Jun, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

MES Configuration, Electronic Batch Records, GxP Compliance, CSV, SAP Integration, PLC/SCADA, Change Management, Data Integrity, Process Automation, Stakeholder Management, Technical Documentation, Analytical Problem Solving

Industry

Pharmaceutical Manufacturing

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. Job Description The MES Specialist is responsible for the implementation, configuration, maintenance, and support of Manufacturing Execution Systems (MES) to enable compliant, efficient, and paperless manufacturing operations. The role ensures seamless integration between shop‑floor equipment, SAP systems, and quality systems while maintaining data integrity, regulatory compliance, and operational excellence in a GMP environment. To Work in shift operation as per production schedule. Responsible to configure, deploy, and support MES applications. Create and maintain Electronic Batch Records (EBR), master recipes, workflows, and system parameters. Perform MES change management including configuration changes, upgrades, and patch installations. Ensure MES compliance with GxP, 21 CFR Part 11, EU Annex 11, and ALCOA+ principles. Support CSV activities including URS, FRS, DS, IQ, OQ, PQ, and risk assessments. Participate in internal and external audits and inspections related to MES. Prepare and maintain SOPs, work instructions, configuration specifications, and technical documentation. Conduct MES training for shop‑floor users and system administrators. Support deviation investigations, CAPAs, and change controls related to MES. Identify opportunities for process automation, paperless manufacturing, and digital maturity improvements. Drive MES performance optimization and best practices adoption. Support data analytics and reporting initiatives for manufacturing KPIs. Qualifications Education Bachelor’s degree in Engineering, Computer Science, Information Technology, or a related field. Experience 4–8 years of experience supporting or implementing MES in a pharmaceutical, biotech, or regulated manufacturing environment. Hands‑on experience with manufacturing processes (e.g., formulation, filling, packaging). Experience working in GMP and validated system environments. Technical Skills Strong knowledge of MES. Experience with SAP integration, automation systems (PLC/SCADA), and databases. Soft Skills Strong analytical and problem‑solving skills. Excellent communication and cross‑functional collaboration abilities. Ability to work independently in a fast‑paced manufacturing environment. Strong documentation and stakeholder management skills. Additional Information About the Department Biologics Currently operates in the Global Biosimilars business - a segment that is poised for attractive and sustained growth over the next 10–15-year time horizon. With a robust portfolio of biosimilar products across key therapeutic areas, covering ~US$80+ Bn in innovator sales – future business pipeline covers a variety of product classes and therapy areas, and new modalities. Fully integrated organization with over two decades of experience in developing, manufacturing and commercializing multiple biosimilar products. With a Product Development engine that has end-to-end capabilities – in-house clone development, upstream and downstream process development, bioanalytical development and proprietary formulation. Supported by a Clinical and Regulatory team with experience in executing complex biosimilar programs with innovative global trial designs. We have a proven experience in commercial-scale manufacturing across a variety of technology platforms with global quality standards and a highly competitive cost structure Rich experience of commercializing high-quality biosimilars in multiple markets with over 900,000 patients having benefited from our products till date. 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/#!/ Job Family: Manufacturing Sub Job Family: Production - Sterile Preferred type of working: On-Premise Years of Experience: 3 - 6 Business unit: Biologics

Responsibilities

Responsible for the implementation, configuration, and support of Manufacturing Execution Systems to enable paperless manufacturing operations. This includes creating Electronic Batch Records and ensuring seamless integration between shop-floor equipment and SAP systems.