Lead India Injectable Manufacturing - IT Operations

Position Title : Lead India Injectable Manufacturing - IT Operations

Location : Bangalore

At VIATRIS, we see healthcare not as it is but as it should be. We act courageously and are uniquely positioned to be a source of stability in a world of evolving healthcare needs.

Viatris empowers people worldwide to live healthier at every stage of life.

We do so via:

• Access – Providing high quality trusted medicines regardless of geography or circumstance;
• Leadership – Advancing sustainable operations and innovative solutions to improve patient health; and
• Partnership – Leveraging our collective expertise to connect people to products and services.

Every day, we rise to the challenge to make a difference and here’s how this role will make an impact:

Role Purpose

The Lead India Injectable Manufacturing IT Operations is responsible for providing strategic leadership and operational oversight for IT systems supporting India's Injectable manufacturing operations. The role will ensure reliable, compliant, secure, and efficient operation of manufacturing IT and OT systems while driving digital transformation initiatives aligned with business objectives.

Key Responsibilities

Manufacturing IT Operations Leadership

• Lead and govern IT operations across Injectable manufacturing facilities in India.
• Ensure high availability and reliability of manufacturing critical systems.
• Drive operational excellence through standardized support processes and service management practices.
• Provide strategic direction for manufacturing technology investments and roadmaps.

Manufacturing Systems & Infrastructure

• Manage and support manufacturing applications including MES, SCADA, Historian, Serialization, Environmental Monitoring, BMS, and shop-floor systems.
• Oversee manufacturing IT infrastructure, networks, servers, and OT environments.
• Ensure seamless integration between manufacturing, quality, and enterprise systems.

Compliance & Quality

• Ensure compliance with GMP, GxP, 21 CFR Part 11and Data Integrity requirements.
• Oversee Computerized System Validation (CSV) lifecycle activities.
• Support regulatory inspections, customer audits, and internal audits.
• Drive effective change control, deviation management, CAPA, and inspection readiness programs.

Cybersecurity & Risk Management

• Implement and maintain OT and manufacturing cybersecurity controls.
• Manage disaster recovery, business continuity, and risk mitigation initiatives.
• Ensure compliance with corporate security standards and policies.

Business Partnership & Digital Transformation

• Partner with Manufacturing, Quality, Engineering, and Supply Chain teams to deliver technology-enabled business solutions.

People & Vendor Leadership

• Lead, mentor, and develop high-performing Manufacturing IT teams.
• Manage strategic technology vendors and service providers.
• Drive performance, accountability, and continuous learning within the organization.

Qualification and Experience

• Bachelor’s degree in engineering, Information Technology, Computer Science, Electronics, or related discipline.
• 15-17 years of overall IT experience.
• Significant experience in Pharmaceutical Manufacturing Site IT Operations.
• Hands-on experience supporting Injectable/Sterile manufacturing environments.
• Strong knowledge of pharmaceutical regulations, data integrity, and compliance requirements.
• Experience managing regulatory inspections and audits.