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Computer System Validation Manager Jobs in Bend, OR

Support computer system validation activities for lab instruments. * Create and manage validation documents, including protocols and reports. * Coordinate on-site repairs and manage vendor ...

Support computer system validation activities for lab instruments. * Create and manage validation documents, including protocols and reports. * Coordinate on-site repairs and manage vendor ...

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Experience with computerized systems validation and equipment qualification. * Experience managing multiple validation projects and competing priorities. * Previous backlog remediation or high-volume ...

Manages installation activities, equipment FAT/SAT execution, and vendor coordination to ensure ... Proficiency in enterprise systems, Microsoft Office, and other office productivity tools, with ...

Manages installation activities, equipment FAT/SAT execution, and vendor coordination to ensure ... Proficiency in enterprise systems, Microsoft Office, and other office productivity tools, with ...

Root cause analysis, systems validation, performance tuning, and capacity management Qualifications Minimum Requirements: Degree in computer science, engineering, or equivalent years training and ...

Job Type Full-time Description Primary Purpose To work with and support the store management team ... Familiar with how to operate a computer system and email.

System Integrator

Bend, OR · On-site

$74 - $92/hr

This reflects management's assignment of essential functions; it does not prescribe or restrict the ... Computer Engineering, Renewable Systems or other relevant experience* Ability to work with sub ...

Showing results 21-40

Computer System Validation Manager information

See Bend, OR salary details

$50.1K

$111.2K

$169.3K

How much do computer system validation manager jobs pay per year?

As of Aug 23, 2026, the average yearly pay for computer system validation manager in Bend, OR is $111,213.00, according to ZipRecruiter salary data. Most workers in this role earn between $78,600.00 and $139,300.00 per year, depending on experience, location, and employer.

What does a computer system validation manager do?

A Computer System Validation Manager is responsible for ensuring that computer systems used in regulated industries, such as pharmaceuticals or biotechnology, meet all required compliance standards. They oversee the planning, execution, and documentation of validation activities to ensure systems are reliable, accurate, and secure. Their duties include managing validation projects, writing protocols, coordinating with IT and quality assurance teams, and ensuring adherence to regulations like FDA 21 CFR Part 11. This role is critical for maintaining product quality and regulatory compliance.

What are the key skills and qualifications needed to thrive as a computer system validation manager, and why are they important?

To thrive as a Computer System Validation Manager, you need expertise in computer system validation regulations (such as GxP, FDA 21 CFR Part 11), strong project management skills, and a background in life sciences or IT. Familiarity with validation lifecycle documentation tools, quality management systems (QMS), and compliance software is often required, along with relevant certifications like PMP or CSV-related credentials. Exceptional attention to detail, analytical thinking, and effective communication are crucial soft skills for coordinating cross-functional teams and ensuring regulatory compliance. These skills and qualifications are vital to ensure validated systems meet regulatory standards, minimize compliance risks, and support organizational quality objectives.

What are some common challenges a computer system validation manager faces during system implementation projects?

A Computer System Validation Manager often encounters challenges such as aligning validation activities with evolving regulatory requirements, managing tight project timelines, and coordinating between multiple stakeholders like IT, Quality Assurance, and business users. Ensuring thorough documentation and traceability, while adapting to technology updates or scope changes, can also be demanding. Proactive communication and strong project management skills are essential to mitigate risks and ensure successful, compliant system implementations.

What is the difference between Computer System Validation Manager vs Computer System Validation Specialist?

AspectComputer System Validation ManagerComputer System Validation Specialist
CertificationsGAMP, CQE, CSQEGAMP, CQE, CSQE
Work EnvironmentManagement, oversight, strategic planningExecution, testing, documentation
Industry UsagePharmaceutical, biotech, regulated industriesPharmaceutical, biotech, regulated industries
Primary FocusLeading validation projects, team coordinationPerforming validation activities, testing

The main difference between a Computer System Validation Manager and a Computer System Validation Specialist lies in their roles. The manager oversees validation projects, manages teams, and ensures compliance, while the specialist executes validation tasks and documents testing procedures. Both roles require similar certifications and are vital in regulated industries like pharmaceuticals and biotech.

What are popular job titles related to Computer System Validation Manager jobs in Bend, OR?

For Computer System Validation Manager jobs in Bend, OR, the most frequently searched job titles are:

Infographic showing various Computer System Validation Manager job openings in Bend, OR as of August 2026, with employment types broken down into 77% Full Time, 6% Part Time, and 17% Contract. Highlights an 83% In-person, 6% Hybrid, and 11% Remote job distribution, with an average salary of $111,213 per year, or $53.5 per hour.

Instrumentation Specialist

Lonza

Bend, OR • On-site

Full-time

Medical, Dental, Vision

Re-posted 6 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. Relocation assistance is available for eligible candidates and their families, if needed.
In this role, you will play a key part in ensuring the reliability and compliance of laboratory instrumentation that supports critical quality control processes. This is an exciting opportunity to contribute to life-saving therapies while developing your technical expertise.
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.
Lonza Pharma & Biotech has an opening for an Instrumentation Specialist at our Bend, OR site. In this role, you will support Quality Control operations by maintaining, calibrating, and troubleshooting analytical laboratory instruments.
What you will get
  • An agile career and dynamic working culture
  • An inclusive and ethical workplace
  • Competitive compensation and performance-based rewards
  • Medical, dental, and vision insurance
  • Opportunities for professional growth and development
  • A collaborative and supportive team environment
What you will do
  • Maintain, calibrate, and troubleshoot analytical laboratory instruments.
  • Develop and maintain validation procedures for laboratory systems.
  • Support computer system validation activities for lab instruments.
  • Create and manage validation documents, including protocols and reports.
  • Coordinate on-site repairs and manage vendor relationships.
  • Order and maintain spare parts and inventory levels.
  • Support audits and provide technical expertise to ensure compliance.
What we are looking for
  • Bachelor's degree or equivalent experience in a related field.
  • Experience working with laboratory instrumentation and systems.
  • Experience maintaining and repairing analytical instruments.
  • Knowledge of regulated environments such as GMP or similar standards.
  • Familiarity with validation or qualification of laboratory equipment.
  • Experience in biotechnology, pharmaceutical, or related industries.
  • Ability to travel between local Bend sites as needed.

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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