Global Documentation and Lifecycle Lead – Standard Materials
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).
What You Will Get
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
What You Will Do
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.
What we are looking for
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.
About Lonza
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.
Searching, interviewing and hiring are all part of the professional life. The TALENTMATE Portal idea is to fill and help professionals doing one of them by bringing together the requisites under One Roof. Whether you're hunting for your Next Job Opportunity or Looking for Potential Employers, we're here to lend you a Helping Hand.
Disclaimer: talentmate.com is only a platform to bring jobseekers & employers together.
Applicants
are
advised to research the bonafides of the prospective employer independently. We do NOT
endorse any
requests for money payments and strictly advice against sharing personal or bank related
information. We
also recommend you visit Security Advice for more information. If you suspect any fraud
or
malpractice,
email us at abuse@talentmate.com.
You have successfully saved for this job. Please check
saved
jobs
list
Applied
You have successfully applied for this job. Please check
applied
jobs list
Do you want to share the
link?
Please click any of the below options to share the job
details.
Report this job
Success
Successfully updated
Success
Successfully updated
Thank you
Reported Successfully.
Copied
This job link has been copied to clipboard!
Apply Job
Upload your Profile Picture
Accepted Formats: jpg, png
Upto 2MB in size
Your application for Global Documentation And Lifecycle Lead
has been successfully submitted!
To increase your chances of getting shortlisted, we recommend completing your profile.
Employers prioritize candidates with full profiles, and a completed profile could set you apart in the
selection process.
Why complete your profile?
Higher Visibility: Complete profiles are more likely to be viewed by employers.
Better Match: Showcase your skills and experience to improve your fit.
Stand Out: Highlight your full potential to make a stronger impression.
Complete your profile now to give your application the best chance!