Lonza
life sciences
QCProjectLead
Neural analysis suggests this role is
optimal for Mid+ candidates.
“QC Project Lead at Lonza. Skills: QC projects, analytical chemistry, quality control, GMP regulations. Lead planning and coordination of QC projects. Collaborate with analytical development”
What You'll Achieve.
ensuring compliance; supporting the delivery of life-changing therapies; ensure compliance; deliverables
Industry & Context.
problem-solving skills; troubleshooting technical challenges; solutions-focused approach
Relocation assistance is available
What They're Looking For.
Must Have
Bachelor's or Master's degree in a scientific field with relevant experience, expertise in analytical chemistry, expertise in quality control environments, Knowledge of GMP regulations, Knowledge of quality systems, Clear written and verbal communication skills in English, Ability to manage multiple priorities, solutions-focused approach
Nice to Have
Experience with QC systems such as MasterControl or similar platforms, problem-solving skills, ability to work across teams
What You'll Do.
Lead planning and coordination of QC projects
Collaborate with analytical development
Collaborate with customers
Collaborate with internal teams
Manage change controls
Manage laboratory investigations
Support QC operations
Troubleshoot technical challenges
Prepare cGMP documentation
Review cGMP documentation
Maintain cGMP documentation
Communicate project progress
Identify continuous improvement initiatives
Implement continuous improvement initiatives
How You'll Work.
Team & Collaboration
Collaborate with analytical development, customers, and internal teams; work across teams
Communication Scope
Clear written and verbal communication skills in English
Process & Methodology
Lead planning and coordination of QC projects, timelines, workflows, risks, deliverables, Manage change controls, Manage deviations, Manage laboratory investigations, Communicate project progress, Escalate risks, Escalate issues
Full Job Description
The actual location of this job is in Bend, Oregon. Relocation assistance is available for eligible candidates and their families, if needed. This role offers an exciting opportunity to lead quality control projects in a dynamic manufacturing environment. You will play a key role in ensuring compliance, coordinating cross-functional activities, and supporting the delivery of life- changing therapies. **This is a fully site-based role.** Working together in person supports close, real-time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards. Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of. ## **What you will get** * An agile career and dynamic working culture * An inclusive and ethical workplace * Compensation programs that recognize high performance * Medical, dental, and vision insurance * Opportunities for professional growth and development * Access to Lonza’s global benefits The full list of our global benefits can also be found at: ## **What you will do** * Lead planning and coordination of QC projects, including timelines, workflows, risks, and deliverables * Collaborate with analytical development, customers, and internal teams on validation and method transfer activities * Manage change controls, deviations, and laboratory investigations to ensure compliance * Support QC operations by troubleshooting technical challenges and assisting analysts * Prepare, review, and maintain cGMP documentation, including SOPs, protocols, and reports * Communicate project progress and escalate risks or issues as needed * Identify and im
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