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Associate Director Quality Jobs in Oregon (NOW HIRING)

Lonza

Associate Director, Quality Assurance

Bend, OR · On-site

This role offers an exciting opportunity to lead a high-performing Quality Assurance team in a regulated pharmaceutical environment. You will play a critical role in ensuring compliance ...

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Associate Director Quality information

What does an associate director quality do?

An Associate Director of Quality oversees quality assurance and quality control processes within an organization, ensuring that products or services meet established standards and regulatory requirements. They lead teams responsible for developing, implementing, and maintaining quality management systems, and often collaborate with other departments to drive continuous improvement. Additionally, they analyze quality data, handle audits, and provide training to staff on best practices. This role is critical for maintaining compliance, customer satisfaction, and the overall integrity of the company's offerings.

What are the key skills and qualifications needed to thrive as an associate director quality?

To thrive as an Associate Director of Quality, you need a thorough understanding of quality management systems, regulatory compliance, and relevant industry standards, usually supported by a bachelor's or master's degree in a scientific or engineering discipline. Familiarity with quality-related tools such as Six Sigma, ISO standards, and electronic quality management systems (eQMS) is typically required, along with certifications like ASQ or Lean Six Sigma. Strong leadership, problem-solving abilities, and effective communication skills help drive cross-functional initiatives and foster a culture of continuous improvement. These skills and qualities are vital to ensure product quality, regulatory adherence, and operational excellence within the organization.

What are some typical challenges faced by an associate director quality, and how can they be addressed?

As an Associate Director of Quality, one common challenge is balancing regulatory compliance with operational efficiency, especially when implementing new quality systems or updates. Navigating cross-functional communication and ensuring all departments adhere to quality standards can also be demanding, as it requires strong leadership and negotiation skills. Staying current with evolving industry regulations and effectively managing audits are key responsibilities, so proactive training and fostering a culture of continuous improvement are essential for success in this role.

What is the difference between Associate Director Quality vs Quality Manager?

AspectAssociate Director QualityQuality Manager
ResponsibilitiesOversees quality strategies, compliance, and cross-departmental initiatives at a higher levelManages daily quality operations, audits, and team supervision
Required CredentialsTypically requires advanced degrees and extensive experience in quality assuranceRequires relevant certifications and experience in quality management
Work EnvironmentStrategic, cross-functional, often involved in policy developmentOperational, focused on process implementation and team management

The Associate Director Quality generally holds a higher strategic role with broader responsibilities compared to the more operational focus of a Quality Manager. While both roles require relevant credentials and experience, the Associate Director is involved in shaping quality policies and ensuring compliance at an organizational level, whereas the Quality Manager oversees daily quality activities and team performance.

What are popular job titles related to Associate Director Quality jobs in Oregon?

For Associate Director Quality jobs in Oregon, the most frequently searched job titles are:

What job categories do people searching Associate Director Quality jobs in Oregon look for?

The top searched job categories for Associate Director Quality jobs in Oregon are:

Associate Director Quality jobs near you
Infographic showing various Associate Director Quality job openings in Oregon as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 17% Part Time, 3% Contract, and 1% Nights. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution.

Associate Director, Quality Assurance

Bend, OR • On-site

Lonza
Biotechnology Research and Development • 10K+ employees
Learn more about Lonzaexternal

Full-time

Medical, Dental, Vision

Re-posted 27 days ago

Lonza rating

8.3

Company rating: 8.3 out of 10

Based on 42 frontline employees who took The Breakroom Quiz

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 lead a high-performing Quality Assurance team in a regulated pharmaceutical environment. You will play a critical role in ensuring compliance, strengthening quality systems, 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 leadership development and career growth
  • Access to Lonza's global benefits

The full list of our global benefits can also be found at: https://www.lonza.com/careers/benefits
What you will do
  • Lead Quality Assurance functions, including training, quality systems, and audit readiness
  • Manage and develop QA teams supporting GMP production and documentation processes
  • Ensure quality systems remain compliant, effective, and aligned with business needs
  • Support manufacturing and development teams to meet regulatory and internal standards
  • Review and approve quality documents, procedures, and specifications
  • Oversee deviation management, CAPA processes, and stakeholder communication
  • Support internal audits, client audits, and regulatory inspections
What we are looking for
  • Bachelor's degree or equivalent experience in a relevant field
  • Extensive experience in the pharmaceutical industry, including work in CDMO environments
  • Proven leadership experience managing teams in regulated quality environments
  • Experience supporting or leading regulatory inspections and audits
  • Strong knowledge of GMP and quality systems
  • Excellent communication skills with the ability to engage diverse stakeholders
  • Ability to manage multiple priorities and drive results in a fast-paced environment
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.

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About Lonza

Sourced by ZipRecruiter

Industry

Biotechnology research and development and pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

Bern, KS, US

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