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Medical Device Qa Jobs in Oregon (NOW HIRING)

Quality Assurance Manager

Bend, OR · On-site

$150 - $200/hr

Join our growing Quality team in Bend, Oregon as a QA Manager. In this leadership role, you will ... Medical, dental and vision insurance. * Opportunities to influence commercial quality strategy and ...

Join our growing Quality team in Bend, Oregon as a QA Manager. In this leadership role, you will ... Medical, dental and vision insurance. * Opportunities to influence commercial quality strategy and ...

What You'll Do As a QA Technician, you'll help ensure our manufacturing processes and products ... Comprehensive employee benefits package, including medical/dental/vision coverage, life and ...

QA Technician

Clackamas, OR · On-site

$23.57/hr

What You'll Do As a QA Technician, you'll help ensure our manufacturing processes and products ... Comprehensive employee benefits package, including medical/dental/vision coverage, life and ...

QA Technician

Clackamas, OR · On-site

$23.57/hr

What You'll Do As a QA Technician, you'll help ensure our manufacturing processes and products ... Comprehensive employee benefits package, including medical/dental/vision coverage, life and ...

QA Technician

Clackamas, OR · On-site

$23.57/hr

What You'll Do As a QA Technician, you'll help ensure our manufacturing processes and products ... Comprehensive employee benefits package, including medical/dental/vision coverage, life and ...

QA Technician

Clackamas, OR · On-site

$23.57/hr

What You'll Do As a QA Technician/Inspector, you'll help ensure our manufacturing processes and ... Comprehensive employee benefits package, including medical/dental/vision coverage, life and ...

Quality Assurance Analyst - HRSN Job Summary This position is responsible for providing timely and ... Knowledge of basic medical terminology * Knowledge of care management platforms and experience with ...

QA Technician

Clackamas, OR · On-site

$23.57/hr

What You'll Do As a QA Technician/Inspector, you'll help ensure our manufacturing processes and ... Comprehensive employee benefits package, including medical/dental/vision coverage, life and ...

Quality Assurance Analyst - HRSN-Job SummaryThis position is responsible for providing timely and ... CareOregon offers medical, dental, vision, life, AD&D, and disability insurance, as well as health ...

Showing results 21-40

Medical Device Qa information

What is a medical device QA?

Medical Device Quality Assurance (QA) professionals are responsible for ensuring that medical devices meet regulatory standards and are safe and effective for use. They develop and implement quality management systems, conduct audits, and oversee documentation throughout the product lifecycle. QA professionals also work closely with engineering, manufacturing, and regulatory teams to identify and resolve quality issues, manage risk, and ensure compliance with industry standards such as ISO 13485 and FDA regulations.

What are the key skills and qualifications needed to thrive as a medical device QA, and why are they important?

To thrive as a Medical Device QA, you need a solid understanding of quality assurance principles, regulatory standards (such as ISO 13485 and FDA 21 CFR Part 820), and a relevant degree in engineering or life sciences. Familiarity with quality management systems (QMS), document control software, and auditing tools is typically required, along with certifications like Certified Quality Auditor (CQA) or Six Sigma. Strong attention to detail, problem-solving abilities, and effective communication help ensure compliance and drive continuous improvement. These skills and qualities are crucial to maintaining product safety, regulatory compliance, and overall quality within the highly regulated medical device industry.

What are some common challenges faced by medical device QA professionals, and how can they be addressed?

Medical Device QA professionals often encounter challenges such as navigating complex regulatory requirements, ensuring product consistency, and keeping up with frequent changes in standards. Addressing these challenges typically involves staying current with FDA and ISO updates, maintaining robust documentation practices, and fostering clear communication with cross-functional teams like R&D and manufacturing. Regular training sessions and proactive risk management strategies also help QA professionals ensure quality and compliance throughout the product lifecycle.

What is the difference between Medical Device Qa vs Medical Device Quality Inspector?

AspectMedical Device QaMedical Device Quality Inspector
CertificationsISO 13485, FDA regulations, Six SigmaISO 13485, FDA regulations, Six Sigma
Work EnvironmentDesign, development, and process oversight in manufacturingInspection and testing on production lines
ResponsibilitiesEnsuring quality systems and complianceInspecting products for defects and conformance

Medical Device Qa professionals focus on quality assurance processes, compliance, and system improvements, while Medical Device Quality Inspectors primarily perform product inspections and defect detection. Both roles require similar certifications and work within the medical device industry, but their daily tasks and focus areas differ significantly.

What are popular job titles related to Medical Device Qa jobs in Oregon?

For Medical Device Qa jobs in Oregon, the most frequently searched job titles are:

Infographic showing various Medical Device Qa job openings in Oregon as of August 2026, with employment types broken down into 79% Full Time, 14% Part Time, and 7% Contract. Highlights an 86% In-person, 7% Hybrid, and 7% Remote job distribution.

Quality Assurance Manager

Lonza

Bend, OR • On-site

$150 - $200/hr

Other

Medical, Dental, Vision

Re-posted 9 days ago


Lonza rating

8.3

Company rating: 8.3 out of 10

Based on 42 frontline employees who took The Breakroom Quiz

25th of 86 rated pharmaceutical


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.
Join our growing Quality team in Bend, Oregon as a QA Manager. In this leadership role, you will help ensure commercial pharmaceutical products meet regulatory requirements while supporting successful product launches, supply reliability, and customer satisfaction.
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.
  • Opportunities to influence commercial quality strategy and business decisions.
  • Exposure to cross-functional leadership across manufacturing, supply chain and commercial teams.
  • The full list of our global benefits can be found at https://www.lonza.com/careers/benefits.
What you will do
  • Manage the timely release of commercial drug products and APIs, ensuring compliance with approved specifications and regulatory requirements.
  • Serve as the primary Quality representative for commercial partners, distributors and key customer accounts.
  • Review and negotiate quality agreements to support successful commercial operations.
  • Oversee quality compliance across distribution, warehousing and third-party logistics providers.
  • Lead investigations into product complaints, identify root causes and implement corrective actions.
  • Partner with Regulatory Affairs to support changes, labeling updates and global regulatory commitments.
  • Monitor quality metrics, support audits and inspections, and drive continuous improvement initiatives.
What we are looking for
  • Bachelor's degree in Pharmacy, Chemistry, Life Sciences or a related field. Advanced qualifications are beneficial.
  • At least five years of experience in pharmaceutical Quality Assurance within a regulated environment.
  • Previous leadership or people management experience.
  • Experience supporting commercial product launches or commercial pharmaceutical operations.
  • Strong knowledge of pharmaceutical quality systems, cGMP requirements and regulatory expectations.
  • Ability to balance compliance requirements with business objectives and delivery timelines.
  • Excellent communication, stakeholder management and cross-functional leadership skills.
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.

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What Lonza employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom


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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