Research Associate Job Opportunity at Dr. Reddy’s
Looking for a rewarding Research Job in the pharmaceutical and biotechnology industry? Here’s an excellent opportunity from Dr. Reddy’s Jobs for talented professionals seeking growth in biologics research and development. The position of Research Associate – Drug Product and Device offers hands-on exposure to formulation development, process optimization, medical device testing, and biosimilar product development. If you’re searching for Research Associate Jobs that combine innovation, scientific excellence, and career advancement, this opportunity in Hyderabad could be your ideal next step.
About Dr. Reddy’s Laboratories
Dr. Reddy’s Laboratories is a leading multinational pharmaceutical company headquartered in India with operations across 66 countries. Since its inception in 1984, the company has focused on making innovative and affordable medicines accessible worldwide. Through Dr. Reddy’s Jobs, professionals gain opportunities to contribute to global healthcare innovation, biosimilar development, and advanced pharmaceutical research. The organization employs more than 24,000 professionals worldwide and continues to invest heavily in scientific research, sustainability, and employee development. The Biologics division is a key growth area, supported by strong capabilities in clone development, process development, formulation development, bioanalytics, clinical research, regulatory affairs, and commercial manufacturing.
Job Details:
- Job Title: Research Associate – Drug Product and Device
- Location: Hyderabad, Telangana, India
Job Description
Job Summary
Dr. Reddy’s Laboratories is seeking an experienced professional to execute experiments focused on process and device optimization for 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 within the Formulation and Drug Product Development (FDPD) function, including process and device optimization experiments.
- Develop and implement suitable characterization methods for pipeline molecules to support container closure selection and process characterization.
- Analyse experimental results and prepare technical reports and presentations for functional review.
- Assist in data acquisition, processing, and compilation, including drafting study protocols and method development reports.
- Maintain accurate records and documentation of all work conducted while ensuring compliance with Safety, Health, and Environment (SHE) and Quality Management Systems.
- Support additional FDPD team assignments as directed by the Team Lead or Functional Head.
Qualifications
- Educational Qualification: Master’s degree in Science (Biochemistry or Biotechnology), or B.Tech in Biotechnology.
- Minimum Work Experience: 2–3 years of relevant experience.
Skills & Attributes
Technical Skills
- Good understanding of process and device functionality.
- Familiarity and prior hands-on experience with medical device testing, particularly Universal Testing Machine (UTM) handling.
- Experience in statistical analysis and data interpretation.
- Knowledge of Good Laboratory Practice (GLP) and Good Manufacturing Practice (GMP).
Behavioural Skills
- Demonstrates excellent learning ability and quickly acquires new knowledge and skills.
- Performance-oriented with a commitment to achieving high standards.
- Motivated and open to exploring new ideas that contribute to innovation.
- Possesses strong interpersonal skills and communicates effectively.
- Maintains high attention to detail and accuracy in experimental work and documentation.
- Capable of working independently as well as collaboratively within a team.
Additional Requirements
- Proficiency in written and spoken English.
- Willingness to work flexible hours as required by experimental needs.
Additional Information
About the Department Biologics
The Biologics division currently operates within the Global Biosimilars business, a segment expected to experience attractive and sustained growth over the next 10–15 years.
Key highlights include:
- A robust biosimilar portfolio spanning key therapeutic areas and covering approximately US$80+ billion in innovator sales.
- A future pipeline comprising diverse product classes, therapy areas, and emerging modalities.
- A fully integrated organization with over two decades of experience in developing, manufacturing, and commercializing multiple biosimilar products.
- End-to-end product development capabilities, including in-house clone development, upstream and downstream process development, bioanalytical development, and proprietary formulation expertise.
- A Clinical and Regulatory team experienced in executing complex biosimilar programs through innovative global trial designs.
- Proven commercial-scale manufacturing capabilities across multiple technology platforms while maintaining global quality standards and a competitive cost structure.
- Extensive experience commercializing high-quality biosimilars across multiple markets, benefiting more than 900,000 patients worldwide.
Benefits Offered
At Dr. Reddy’s, employees are actively supported in accelerating career growth and professional development through personalized learning programs.
Benefits include:
- Joining and relocation support.
- Family support programs, including maternity and paternity benefits.
- Learning and development opportunities.
- Medical coverage for employees and their families.
- Life insurance coverage for employees.
- Access to essential work equipment.
- Benefits aligned with leading industry standards.
