The actual location of this job is in Hyderabad, India Relocation assistance is available for eligible candidates and their families, if needed.
Lead and shape the qualification, validation, and computerized systems compliance strategies for global cGMP pharmaceutical manufacturing operations from the Lonza Capability Center (LCC) in Hyderabad In this high-impact executive role, you will lead a dedicated team of QA professionals, drive compliance across international regulatory standards, and elevate global quality engineering practices
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.
An inclusive and ethical workplace.
Compensation programs that recognize high performance.
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
cGMP Compliance Leadership: Maintain overall accountability for qualification and validation compliance across equipment, facilities, utilities, and computerized systems for cGMP pharmaceutical manufacturing
Team Leadership & Development: Direct, enable, and mentor multidisciplinary QA C&Q teams (≥15 FTEs covering Equipment, CSV, Facilities/Utilities, and Enabling Qualification) to achieve consistent high performance
End-to-End Lifecycle QA Oversight: Oversee complete commissioning and qualification (C&Q) lifecycles—from initial qualification through routine operations, periodic reviews, and decommissioning
Global Harmonization & Representation: Serve as the senior Global QA representative for LCC Quality in global/cross-functional forums to define and harmonize global engineering and quality standards
Regulatory Compliance & Inspection Readiness: Translate evolving global regulatory guidance (e.g., FDA, Swissmedic, EMA) and inspection outcomes into actionable quality strategies and continuous inspection readiness
Data Integrity & Process Improvement: Evaluate and strengthen data integrity practices, driving standardized processes and continuous improvement initiatives across qualification lifecycles
Cross-Functional Stakeholder Alignment: Partner closely with Global & Site Engineering Leads, LCC Quality Leadership, and site QA teams to ensure seamless project execution and alignment
Education: Bachelor’s or Master’s degree in Engineering (Biologics or Chemical) or Biological Sciences
Industry Experience: 10+ years of relevant experience in a regulated pharmaceutical environment covering QA, manufacturing, engineering, R&D, or regulatory affairs
Regulatory Mastery: Proven management experience in EMA/FDA-regulated environments with in-depth knowledge of cGMP, ICH, PIC/S, EU, and US regulatory standards
Facility & C&Q Lifecycle Expertise: Demonstrated experience in QA aspects of facility design, CQV lifecycle management, CSV, equipment validation, change management, and decommissioning
People & Matrix Leadership: Strong people management track record in complex global matrix environments, with proven capability in resource allocation, budget management, and coaching
Strategic & Analytical Skills: Advanced problem-solving, project management, and risk-based decision-making capabilities
Communication & Influence: Exceptional English communication and interpersonal skills, with the ability to influence cross-functional leaders across global sites
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.
Ready to shape the future of life sciences? Apply now.
Lonza is a pioneer and world leader in the CDMO industry, setting the pace with cutting-edge science, smart technology, and lean manufacturing. United by a common purpose, we turn our customers’ breakthrough innovations into viable therapies and manufacture the medicines of tomorrow.
Founded in Switzerland in 1897, our company is the first and original CDMO, and today we are more dynamic, agile and forward-focused than ever before. As one of the largest Western CDMOs, we bring together a global team of around 18,500 colleagues across five continents to deliver comprehensive, integrated solutions for our customers' complex needs.
For our customers and their patients, we bring quality, safety and reliability to bring life-enhancing and life-saving treatments to market at speed and at scale. For our colleagues, we strive to create a sense of belonging and inclusion where every person can thrive and bring their best.
