Team Member MSAT Injectables

Why This Role Matters
Manufacturing Science and Technology (MSAT) serves as the bridge between product development and commercial manufacturing. In the injectable pharmaceutical segment, precision, sterility assurance, regulatory compliance, and process robustness are critical to patient safety and product success.
At Dr. Reddy's Laboratories Limited, the MSAT Injectables team plays a key role in ensuring seamless technology transfer, lifecycle management (LCM), and continuous improvement of sterile products. This role directly contributes to successful product launches, regulatory approvals, and sustained commercial supply.
Working within the IPDO business unit in Visakhapatnam offers exposure to advanced injectable manufacturing systems, structured quality frameworks, and global regulatory expectations.

Job Description
We are looking for a skilled and detail-oriented professional to join the MSAT Injectables team as a Team Member – Technology Transfer (Parenteral). The selected candidate will support lifecycle management activities, scale-ups, site transfers, and commercial batch execution for sterile injectable products.
The role requires strong technical understanding of parenteral manufacturing processes, change control systems, and regulatory documentation. The candidate will work closely with cross-functional teams to ensure smooth product transfer, compliance with GMP requirements, and continuous process improvement.
This is a full-time, on-premise position based in Visakhapatnam, Andhra Pradesh, under the Engineering & Science job family.

Key Features of the Role
• Exposure to sterile injectable manufacturing and technology transfer
• Involvement in lifecycle management (LCM) documentation
• Participation in site transfers, line transfers, and commercial scale-ups
• Engagement in regulatory audits and compliance activities
• Cross-functional collaboration across Production, QA, QC, and Regulatory teams
• Opportunity to work within a globally recognized pharmaceutical organization

Responsibilities
• Prepare, review, and approve technical protocols, reports, and product impact assessments related to lifecycle management
• Initiate and manage change controls, incidents, and risk assessments linked to technology transfer
• Support new product introduction (NPI), scale-ups, line transfers, and site-to-site commercial batch transfers for injectable products
• Coordinate with cross-functional teams for documentation and execution of transfer activities
• Support investigations for non-conformances including Incidents, OOS, OOT, and Market Complaints
• Conduct root cause analysis and perform impact assessments for deviations
• Provide technical input for process improvements and regulatory deficiency responses
• Assist in audit preparation and regulatory inspections to ensure timely product approvals
• Analyze manufacturing data to identify trends and optimization opportunities
• Ensure adherence to Good Manufacturing Practices (GMP) and global regulatory standards

Required Qualifications

Educational Requirements:
• Bachelor of Technology / Bachelor of Engineering (Chemical Engineering)
• Bachelor of Pharmacy (B.Pharm)
• Master of Pharmacy (M.Pharm)

Experience and Skills:
• 3–6 years of relevant experience in MSAT, technology transfer, or injectable manufacturing
• Strong understanding of sterile product manufacturing processes
• Hands-on experience in change control and deviation management systems
• Knowledge of GMP requirements and regulatory compliance frameworks
• Experience in handling investigations such as OOS, OOT, and market complaints
• Analytical mindset with strong data interpretation skills
• Ability to work collaboratively with cross-functional teams
• Strong documentation and technical writing capability

Salary Insights
Compensation is competitive and aligned with industry standards for MSAT professionals with 3–6 years of experience in injectable manufacturing. The final package will depend on technical expertise, prior technology transfer exposure, and regulatory experience. Benefits typically include performance incentives, health coverage, and structured career growth opportunities.

Company Overview
Dr. Reddy's Laboratories Limited is a global pharmaceutical organization committed to providing affordable and innovative medicines. The company operates across multiple therapeutic segments and has strong capabilities in research, development, manufacturing, and global commercialization.
The IPDO (Integrated Product Development Organization) unit focuses on efficient product development and technology transfer, ensuring high-quality and compliant manufacturing across global markets.

FAQs

• Is prior injectable experience mandatory?
Yes, experience in sterile or parenteral manufacturing environments is strongly preferred.

• Does this role involve regulatory interaction?
Yes, the role supports audit readiness, regulatory deficiency responses, and compliance documentation.

• What type of working model is followed?
This is an on-premise, full-time position based in Visakhapatnam.

• What kind of career growth can be expected?
Opportunities include progression within MSAT, technology transfer leadership roles, or advanced manufacturing science positions.

Application Tips
• Highlight experience in injectable or sterile manufacturing
• Mention involvement in technology transfer or scale-up projects
• Showcase deviation handling, change control, and audit participation experience
• Emphasize GMP compliance knowledge and documentation accuracy
• Provide examples of cross-functional coordination and data-driven process improvements