Global Documentation and Lifecycle Lead

Hyderabad, India
 

The Global Documentation and Lifecycle Lead – Standard Materials plays a critical role in ensuring compliant, efficient, and harmonized document lifecycle management across Lonza’s global network. This is an exciting opportunity to shape global documentation strategies, drive standardization initiatives, and support operational excellence across the material lifecycle.

This is an office-first role. Working together in person supports close, real-time collaboration and team alignment, enabling us to deliver our best work. You will work primarily in the office, with the flexibility to work remotely for 20% of your time (one day per week).
 

• An agile career and dynamic working culture.
• The opportunity to influence global documentation and quality processes across multiple sites.
• An inclusive and ethical workplace that values diverse perspectives.
• Compensation programs that recognize high performance.
• Opportunities to collaborate with global cross-functional teams and build expertise in quality systems and lifecycle management.
• A variety of benefits dependent on role and location.

The full list of our global benefits can be found here: https://www.lonza.com/careers/benefits
 

• Lead the global lifecycle management of controlled documents related to Standard Materials, ensuring compliance with Quality Management System (QMS) requirements and regulatory expectations.
• Drive the harmonization and standardization of documentation practices across global manufacturing sites for raw materials, chemicals, and single-use systems.
• Develop, maintain, and continuously improve document control processes, templates, workflows, and governance standards.
• Partner with Quality, Regulatory, Manufacturing, Procurement, Supply Chain, and IT teams to ensure documentation effectively supports global material lifecycle management.
• Champion process improvement initiatives, leveraging digital solutions and automation to enhance document control efficiency and reduce complexity.
• Ensure inspection readiness through accurate, complete, and retrievable documentation that meets GxP, data integrity, and Good Documentation Practice (GDocP) requirements.
• Monitor documentation performance metrics, provide stakeholder training and guidance, and drive continuous improvement through data-driven decision-making.
   

• Experience working in a GxP-regulated environment, preferably within biopharmaceutical, pharmaceutical, life sciences, or related regulated industries.
• Strong expertise in document control, quality systems, lifecycle management, and Good Documentation Practice (GDocP).
• Hands-on experience with electronic document management and quality management systems such as Veeva, TrackWise, DMS, or similar platforms.
• Ability to develop structured documentation, standard operating procedures (SOPs), workflows, and process maps that support compliance and operational excellence.
• Proven capability to collaborate effectively with global stakeholders and influence outcomes within a matrix organization.
• Bachelor’s degree in Life Sciences, Quality Management, Information Management, or another relevant discipline, or equivalent experience gained through related roles.
• Excellent communication, analytical, organizational, and continuous improvement skills, with Lean Six Sigma knowledge considered advantageous.
   

At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of.

Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment for all employees. If you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board.