Chemical Engineering Job Opening – MSAT Injectable at Dr. Reddy’s
Are you looking for a rewarding Chemical Engineering job that offers long-term growth and the chance to be part of a purpose-driven Dr. Reddy’s career? The MSAT Injectable role in Visakhapatnam provides the opportunity to work with advanced technology, support product lifecycle management, and contribute to meaningful healthcare solutions. With a strong focus on innovation, science, and patient impact, this position is ideal for professionals seeking to advance in the pharmaceutical industry.
Company Description
Dr. Reddy’s Laboratories Ltd. is a global pharmaceutical leader dedicated to expanding access to affordable and innovative medicines. Since its founding in 1984, the company has grown from a small team into a multinational organization with research centers, manufacturing facilities, and commercial operations across 66 countries. With over 24,000 employees driven by the credo Good Health Can’t Wait, Dr. Reddy’s builds meaningful pharmaceutical careers rooted in science, innovation, and patient impact. The company offers strong opportunities for those seeking a long-term Dr. Reddy’s career, including roles like Chemical Engineering job positions and specialized MSAT Injectable functions. Focused on sustainability, deep science, and global healthcare solutions, Dr. Reddy’s remains a trusted partner in improving patient lives worldwide
.Job Details
- Job Post: Team Member MSAT Injectable
- Location: Visakhapatnam, Andhra Pradesh, India
- Experience: 3 – 6
- Qualifications: Bachelor of Technology or Bachelor of Engineering (Chemical engineer)/Bachelor of Pharmacy/Master of Pharmacy
Job Description
- 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 supporting 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.
