MSc Biotechnology Job Vacancies at Dr Reddy’s, Apply Online
Team member – Drug Substance
Hyderabad, Telangana, India
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 summary
We are looking for an individual to execute downstream/upstream MES (E BPR) unit operations, ensuring documentation and compliance within GMP (Good Manufacturing Practices), regulatory, and organizational guidelines. The objective is to produce products within defined volumes and timelines while maintaining compliance with quality standards, GMP, and other regulatory and statutory requirements, as per the schedule.
Roles & Responsibilities
• You will execute unit operations within Upstream according to the BPR (Batch Production Record), conduct activities to support production schedules, obtain and stock supplies as required, prepare media, buffers, and solutions necessary for unit operations, and perform routine cleaning and support activities in GMP Manufacturing areas.
• You will perform routine process area cleaning, autoclave operation, manual cleaning and sterilization of components and parts, monitoring processes and results, suggesting methods to ensure process success, and interfacing with process automation systems.
• You will issue discrepancies, collaborate with cross-functional departments to close them, implement corrective actions, and comply with GMP and safety standards, for designated manufacturing equipment.
• You will complete batch documentation in alignment with GMP, ensuring data collection and maintenance meet cGMPs (Current GMP), company standards, policies, and regulatory requirements, and supporting timely root cause investigations and CAPA (Corrective and Preventive Actions) completion.
• Your other responsibilities include maintaining manufacturing equipment for correct functionality and calibration compliance, operating within validated process parameters, and supporting qualification and validation activities.
• Emphasizing safety awareness and continuous improvement, you will actively adhere to safety rules and promptly report unsafe matters and near misses/accidents.
Qualifications
Educational qualification: A Graduation in Chemical Engineering or Biotechnology, or a Post-Graduation in Science
Minimum work experience: 3 years of experience in working on Biosimilar/Vaccine Products
Skills & attributes:
Technical Skills
• Comprehensive understanding of process manufacturing.
• Expertise in quality systems implementation and adherence to safety norms, ensuring compliance with industry standards.
• Practical experience and hands-on knowledge of Upstream operations.
• Knowledge of equipment and processes, and proficiency in cleaning validation in the pharmaceutical manufacturing context.
• Understanding and knowledge of Clean-in-Place (CIP) and Sterilize-in-Place (SIP) systems.
Behavioral skills
• Possesses effective listening abilities, fostering clear communication and understanding.
• Pays meticulous attention to detail, ensuring precision in tasks and work.
• Prioritizes and is aware of deadlines, ensuring timely completion of tasks.
• Demonstrates analytical skills and the ability to troubleshoot effectively.
• Possesses strong interpersonal skills and collaborates effectively within a team.
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