Team Member - Manufacturing (Derma) at Dr Reddy's Laboratories Limited

, Andhra Pradesh, India -

Full Time

Start Date

Immediate

Expiry Date

20 Aug, 26

Salary

0.0

Posted On

22 May, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Derma Manufacturing, cGMP Compliance, SOP Execution, Equipment Operation, Documentation Accuracy, Data Integrity, Line Clearance, CIP/COP Procedures, EHS Guidelines, 5S Methodology, Teamwork, Shift Discipline

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 Job Purpose To operate and support Derma (topical) manufacturing lines such as creams, ointments, gels, lotions, and ointment filling/packing lines, by executing production activities in compliance with cGMP, SOPs, safety, and quality requirements, ensuring consistent product quality and uninterrupted production. Roles & Responsibilities 1. Manufacturing Operations (Derma) Operate and support dermatological production processes such as: Cream, ointment, gel, lotion manufacturing Mixing, homogenization, emulsification Transfer and holding operations Execute activities as per approved BMR/BPR and SOPs. Set up, operate, and monitor manufacturing equipment like mixers, homogenizers, vessels, transfer pumps, etc. Ensure adherence to process parameters (time, temperature, speed, vacuum, etc.). 2. Equipment Operation & Cleaning Perform equipment cleaning, assembly, disassembly, and line setup as per SOPs. Execute line clearance and area clearance before batch start and after batch completion. Follow CIP / COP procedures, where applicable. Report equipment abnormalities, breakdowns, or deviations to supervisors. 3. cGMP, Quality & Compliance Strictly follow cGMP, GDP, data integrity (ALCOA+), and hygiene practices. Perform operations only with QA‑released raw materials and approved documents. Ensure proper batch traceability and identification at all stages of manufacturing. Support deviations, investigations, CAPAs, and rework activities as instructed. 4. Documentation Record all manufacturing activities accurately in BMR/BPR and logbooks. Ensure documentation is legible, contemporaneous, and error‑free. Perform corrections strictly as per SOP without data manipulation. 5. Coordination with Cross‑Functional Teams Coordinate with Warehouse for timely receipt of raw materials and consumables. Coordinate with Quality Assurance (QA) for line clearance, in‑process controls, and batch closure. Support Quality Control (QC) during in‑process sampling and observations. 6. Safety, EHS & Housekeeping Follow EHS guidelines, PPE usage, and MSDS instructions during chemical handling. Ensure personal hygiene and gowning compliance as per clean area requirements. Maintain 5S, cleanliness, and discipline in production areas. Report incidents, near misses, or unsafe conditions immediately. 7. Continuous Improvement & Team Participation Participate in Kaizen, TPM, AWT / Work Circles, and process improvement activities. Support validation, scale‑up, and trial batches under supervision. Assist in training of new operators when required. Qualifications Educational Qualification Diploma in Mechanical / Electrical / Chemical / Pharmacy B.Sc. (Chemistry) / B.Pharmacy (preferred for Derma lines) Experience 1–5 years of experience in Derma / Topical dosage manufacturing in a pharmaceutical plant. Experience with US‑FDA / EU‑GMP / WHO‑GMP regulated environments is an advantage. Key Skills & Competencies Knowledge of Derma manufacturing processes Understanding of cGMP and SOP compliance Basic equipment operating knowledge Documentation accuracy and attention to detail Teamwork and shift discipline Willingness to work in shift operations Additional Information About the Department: Global Generics India Global Generics India business journey began in 1986. In the last three decades, we have grown as a trusted name in the healthcare industry and rank as one of the top 10 Pharma Companies in the Indian Pharma Market (IPM) as per IQVIA MAT (November 2022). Our commitment to Lead Ahead has helped us move ranks from 16th position to 10th position (IPM) in the last four years. We are a fast-growing organization with double-digit growth and significant market share in domestic markets. Currently, we rank among the top 5 in oncology, anti-allergy, and gastrointestinal diseases and the top 10 in a few other therapy areas. Our focus is on leveraging our digital capabilities, collaborations, innovations, and inorganic opportunities to become the top 5 companies in the Indian Pharma Market. " 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 - OSD Preferred type of working: On-Premise Years of Experience: 1 - 3 Business unit: GMO

Responsibilities

Operate and support dermatological manufacturing lines for creams, ointments, and gels in compliance with cGMP and SOPs. Ensure consistent product quality through equipment monitoring, accurate documentation, and coordination with QA and QC teams.