Top 1 Lead associate Jobs in Bend, Or

Associate Director, Quality Assurance, Transformational Lead
Lonza —Bend, OR
- Full-time
- Engineering
- Conflict management
- Agile
- Relocation assistance
- Health insurance
1d

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Associate Director, Quality Assurance, Transformational Lead

Lonza -
Bend, OR

Apply Now

Job Details

Full-time
1 day ago

Benefits

Relocation assistance
Health insurance
Dental insurance
Vision insurance

Qualifications

Quality control corrective actions
Preventive action implementation
Drug regulation
Production deviation management
Corrective and preventive actions (CAPA)
GMP
Pharmaceutical company experience
Quality assurance experience within pharmaceutical industry
Conflict management
Regulatory/legal compliance standards in production
Legal compliance
Cross-functional team management
Project stakeholder communication
Stakeholder relationship building
Cross-functional communication
Pharmaceutical manufacturing facility experience
Stakeholder management

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.

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 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 you to be part of.

We're looking for an Associate Director, Quality Assurance (QA) Transformational Lead to champion a culture of continuous improvement by influencing cross-functional teams and stakeholders to embrace modern, data-driven quality practices. Through strategic leadership and relationship-building, this role inspires organizational alignment to deliver impactful process changes while ensuring unwavering compliance with cGMP and global regulatory standards.

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.

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.

Exposure to cross-functional and global quality initiatives.

Access to Lonza's comprehensive benefits programs.

What you will do:

Drive Culture Change: Lead site-wide initiatives to shift the organizational mindset toward proactive quality, continuous improvement, and a robust "Quality Culture."

Optimize QA Workflows: Map, analyze, and redesign core QA processes—such as deviations, change controls, and batch release—to eliminate bottlenecks and reduce cycle times.

Ensure Regulatory Compliance: Align all transformation strategies with current global regulations, including FDA, EMA, and ICH guidelines, ensuring a state of constant inspection readiness.

Harmonize Global Standards: Collaborate with global quality networks to standardize procedures across different manufacturing sites and eliminate localized process variances.

Lead Risk Management: Champion advanced Quality Risk Management (QRM) methodologies, integrating data-driven risk assessments into the daily manufacturing lifecycle.

Manage Cross-Functional Stakeholders: Serve as the primary liaison between QA, Manufacturing, IT, and Supply Chain teams to ensure unified execution of modernization projects.

Define Performance Metrics: Establish, track, and report on key performance indicators (KPIs) and data maturity models to measure the financial and operational impact of QA changes.

Upskill the Workforce: Design and deliver training programs that equip the quality and operations teams with the skills needed to operate new digital tools and agile workflows.

What we are looking for:

Bachelor's degree in engineering, life sciences, or related field.

10+ years of quality assurance experience within the pharmaceutical, biotechnology, or related industry.

Expertise in GMP/FDA regulations (including CFR Parts 11, 210, 211, and 820) with a proven track record managing quality systems, investigations, change controls, and CAPA programs within pharmaceutical manufacturing operations.

Stakeholder Engagement & Rapport: Ability to build trust and open communication channels across traditionally siloed departments like Manufacturing, Supply Chain, and Maintenance.

Influence Without Authority: Capability to drive strategic quality initiatives and process changes in other departments without having direct managerial control over those teams.

Conflict Resolution: Expert navigation of friction when quality requirements clash with aggressive production deadlines or commercial goals.

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 offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. 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.

Apply Now

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