MS&T Specialist

Teva Active Pharmaceutical Ingredient; Gajraula; On-site; INR 900,000 - 1,300,000; Full time

Job summary

Teva Active Pharmaceutical Ingredient in India seeks an experienced chemical engineer to lead process development and site transfers. You will map processes to capacity, perform simulations with Dynochem, and coordinate cross-functional teams to meet timelines.

Responsibilities include safety studies, cGMP-compliant pre-validation, and change control documentation. The role emphasizes project management, plant infrastructure analysis, and effective communication with management.

Qualifications

• 6–10 years of pharma API industry experience.
• B.Tech in Chemical Engineering or equivalent.
• Experience with process evaluation and plant infrastructure analysis.

Responsibilities

• Lead new product development and site transfer initiatives.
• Map processes to plant capacity and select equipment.
• Conduct process simulations and prepare process diagrams.
• Coordinate cross-functional teams for evaluations and timelines.
• Develop and manage project schedules using Gantt charts.
• Conduct safety assessments including HAZOP.
• Prepare validation batches per cGMP guidelines.
• Prepare documentation and change control reviews.

Skills

Process engineering

Project management

Cross-functional coordination

Safety assessments

cGMP compliance

Education

B.Tech-Chemical

Tools

Dynochem

Job description

Job Description

• Lead new product development and site transfer initiatives, including detailed process evaluation and plant infrastructure analysis
• Map processes to available plant capacity by selecting appropriate equipment, determining stoichiometry ratios, and defining unit operations
• Conduct process simulations using tools such as Dynochem and prepare block and process flow diagrams with raw material consumption norms, effluent load, and solvent specifications
• Coordinate cross-functional teams (local and global) to deliver comprehensive evaluations including investment requirements and project timelines
• Develop and manage project schedules using Gantt charts for routine tracking and successful project completion
• Conduct safety assessments including HAZOP studies and implement safety data requirements in accordance with plant standards
• Execute and document pre-validation and validation batches in compliance with cGMP guidelines
• Prepare statutory documentation and change control reviews for new product launches, process stages, and campaigns
• Evaluate utility requirements based on process specifications and coordinate facility modification activities
• Provide chemical engineering support to resolve unit operation challenges and troubleshoot process-related issues in the plant
• Manage technology transfer activities, risk mitigation, and escalation protocols
• Present project progress and findings to management Qualifications

Experience: 6-10 Years in Pharma API Industry

Qualification : B.Tech-Chemical