Research Associate - Drug Product and Device at Dr Reddy's Laboratories Limited

Hyderabad, Telangana, India -

Full Time

Start Date

Immediate

Expiry Date

23 Jun, 26

Salary

0.0

Posted On

25 Mar, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Process Optimization, Device Optimization, Biologic Molecules, Characterization Methods, Container Closure Selection, Statistical Analysis, Data Interpretation, Good Laboratory Practice (GLP), Good Manufacturing Practice (GMP), Interpersonal Skills, Attention To Detail, UTM Handling, Experimental Design, Technical Reporting, Data Acquisition, Protocol Drafting

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 summary We are seeking an experienced professional to execute experiments for process and device optimization of various biologic molecules. The role involves planning and conducting experiments, analysing results, and ensuring compliance with safety and quality standards. Roles & Responsibilities Execute assigned projects in the Formulation and Drug Product Development (FDPD) function, including process and device optimization experiments. Develop and implement suitable methods for characterization of pipeline molecules, supporting container closure selection and process characterization. Analyse experimental results, prepare technical reports and presentations for functional review. Assist in data acquisition, processing, and compilation, including drafting study protocols and method development reports. Maintain proper records and documentation of all work conducted, ensuring compliance with Safety, Health, and Environment (SHE) and Quality Management Systems. Support additional FDPD team assignments as required by Team Lead or Functional Head. Qualifications Educational qualification: A Master's degree in Science (Biochemistry or Biotechnology) or B.Tech (Mechanical/Biotechnology) is required. Minimum work experience: 2-3 years of relevant experience Skills & attributes: Technical Skills Good understanding of process and device functionality. Familiarity and some previous hands-on experience with medical device testing, especially UTM handling. Experience with statistical analysis and data interpretation. Knowledge of Good Laboratory Practice (GLP) and Good Manufacturing Practice (GMP). Behavioural skills Demonstrates excellent learning ability, quickly acquiring new knowledge and skills. Is performance-oriented, consistently striving for high standards and achievement. Displays motivation and readiness to explore new ideas, contributing to innovation. Possesses good interpersonal skills, fostering positive relationships and effective communication. Exhibits strong attention to detail and accuracy in experimental work and documentation. Demonstrates ability to work independently and as part of a collaborative team. Additional requirements Proficiency in English, both written and verbal. Willingness to work flexible hours when required by experimental needs. 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: Research & Development Sub Job Family: Formulation R&D - Biosimilar Preferred type of working: On-Premise Years of Experience: 3 - 6 Business unit: Biologics

Responsibilities

The professional will execute assigned projects in Formulation and Drug Product Development, focusing on process and device optimization experiments for various biologic molecules. This includes developing characterization methods, analyzing results, preparing technical reports, and ensuring compliance with safety and quality standards.