Chemical Engineering Job at Dr. Reddy’s Laboratories | Apply Now
Are you looking for a Chemical Engineering job or a manufacturing job with a global pharmaceutical leader? Dr. Reddy’s Laboratories offers rewarding careers that combine science, innovation, and sustainability. As a Team Member – MSAT Injectable in Visakhapatnam, you’ll apply your technical and data analysis skills to help deliver affordable, high-quality medicines—because at Dr. Reddy’s, Good Health Can’t Wait.
About Dr. Reddy’s Laboratories
Dr. Reddy’s Laboratories is a global pharmaceutical company committed to accelerating access to affordable, innovative medicines. With 24,000 employees across 66 countries, the company leads in Chemical Engineering, manufacturing, and data analysis-driven innovation. It delivers world-class formulations through advanced R&D, sustainable operations, and strong ethical values. Dr. Reddy’s fosters a diverse, inclusive culture, empowering professionals to build meaningful careers in science and technology. Guided by the principle Good Health Can’t Wait, the company continues to shape the future of global healthcare through innovation, excellence, and integrity.
Job Details
- Job Title: Team Member MSAT Injectable
- Location: Visakhapatnam Rural Mandal, India
- Qualifications: Bachelor of Technology or Bachelor of Engineering (Chemical engineer)/Bachelor of Pharmacy/Master of Pharmacy.
Job Description
Suppose you’re seeking a Chemical Engineering job or a manufacturing job in the pharmaceutical sector. In that case, this role offers the chance to work on high-impact injectable products while driving process improvement through data analysis and technology innovation.
Job Responsibilities
- Prepare, review, and approve technical protocols, reports, and product impact assessments related to product lifecycle management (LCM).
- Initiate, change controls, incidents, and risk assessments related to technology transfer activities.
- Support technology transfer activities for new products, scale-ups, line transfers, and site-to-site commercial batches for injectable products.
- Coordinate with cross-functional teams for execution and documentation of new products, scale-ups, and line or site transfers.
- Support investigations for non-conformances (Incidents, OOS, OOT, Market Complaints) through root cause analysis and impact assessments.
- Provide technical support for process changes and improvements along with addressing regulatory deficiencies and support audits to ensure timely product approvals.
- Collaborate with cross-functional teams to improve manufacturing processes.
- Conduct data analysis to identify trends and opportunities for process improvement.
- Assist in the implementation of process improvements and new technologies.
- Ensure compliance with Good Manufacturing Practices (GMP) and regulatory requirements.
