Lonza
biopharmaceutical
CQVEngineer
Neural analysis suggests this role is
optimal for Mid+ candidates.
“CQV Engineer at Lonza. Skills: Validation, Commissioning, Qualification. Support validation and commissioning activities. Ensure equipment, systems, and processes meet quality and compliance standards”
What You'll Achieve.
Enable the delivery of life-changing therapies; Ensure equipment, systems, and processes meet quality and compliance standards
Industry & Context.
problem-solving skills
Relocation assistance is available
What They're Looking For.
Must Have
Experience in commissioning, qualification, and validation or similar environments, Knowledge of FDA, cGMP, and industry guidelines such as ICH, ISPE, or ISO, Proficiency with Microsoft Word and Excel, problem-solving skills, ability to work across teams, Clear written and verbal communication skills, Interest in improving systems and supporting safe, effective drug development
Nice to Have
High school diploma or GED degree in engineering or related field
What You'll Do.
Support validation and commissioning activities
and processes meet quality and compliance standards
Partner with engineering
and manufacturing teams
Support project execution
Troubleshoot and improve equipment
and execute qualification protocols
Identify risks to product quality
Support mitigation strategies
Generate validation reports
Maintain compliant documentation
Manage and close deviations or non-conformances
Support development of engineering and validation documentation
How You'll Work.
Team & Collaboration
Work together in person supports close, real-time collaboration; Talented people working together; Partner with engineering, quality, and manufacturing teams; ability to work across teams
Communication Scope
Clear written and verbal communication skills
Full Job Description
The actual location of this job is in Bend, Oregon (USA). Relocation assistance is available for eligible candidates and their families, if needed. This role offers an exciting opportunity to support validation and commissioning activities in a regulated biopharmaceutical environment. You will play a key role in ensuring equipment, systems, and processes meet quality and compliance standards that enable 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 * Exposure to cross-functional teams and impactful projects ## **What you will do** * Partner with engineering, quality, and manufacturing teams to support project execution * Troubleshoot and improve equipment, processes, and systems * Write, review, and execute qualification protocols, including IQ, OQ, and PQ * Identify risks to product quality and support mitigation strategies * Generate validation reports and maintain compliant documentation * Manage and close deviations or non-conformances during testing activities * Support development of engineering and validation documentation ## **What we are looking for** * High school diploma or
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