CQV Engineer
Bend, OR · On-site
CQV Engineer Bend, OR 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 ...
Bend, OR · On-site
CQV Engineer Bend, OR 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 ...
Bend, OR · On-site
CQV Engineer Bend, OR 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 ...
Bend, OR · On-site
CQV Engineer Bend, OR 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 ...
Bend, OR · On-site
CQV Engineer Bend, OR 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 ...
Bend, OR · On-site
High School Diploma or GED required; engineering degree preferred. * Experience in CQV and temperature mapping. * Understanding of FDA, ICH, ISPE, and ISO guidelines. * Proficiency with Microsoft ...
Bend, OR · On-site
High School Diploma or GED required; engineering degree preferred. * Experience in CQV and temperature mapping. * Understanding of FDA, ICH, ISPE, and ISO guidelines. * Proficiency with Microsoft ...
Bend, OR · On-site
High School Diploma or GED required; engineering degree preferred. * Experience in CQV and temperature mapping. * Understanding of FDA, ICH, ISPE, and ISO guidelines. * Proficiency with Microsoft ...
Bend, OR · On-site
High School Diploma or GED required; engineering degree preferred. * Experience in CQV and temperature mapping. * Understanding of FDA, ICH, ISPE, and ISO guidelines. * Proficiency with Microsoft ...
Bend, OR · On-site
CQV Validation Specialist / CSV/CQV Specialist Location: Bend, OR (Onsite) Duration: 6-9 Month ... Partner with Quality Control, Instrumentation, Engineering, Automation, Quality Assurance, and ...
Bend, OR · On-site
CQV Validation Specialist / CSV/CQV Specialist Location: Bend, OR (Onsite) Duration: 6-9 Month ... Partner with Quality Control, Instrumentation, Engineering, Automation, Quality Assurance, and ...
Bend, OR · On-site
$70.92 - $99.29/hr
Validation Engineer 2 CSV/CQV Specialist Location: 1201 NW Wall Street, Bend, OR 97703 Work Model: Full-Time, Onsite Contract Duration: 69 Months (Potential for Extension or Full-Time Conversion) Pay ...
Bend, OR · On-site
$70.92 - $99.29/hr
Validation Engineer 2 CSV/CQV Specialist Location: 1201 NW Wall Street, Bend, OR 97703 Work Model: Full-Time, Onsite Contract Duration: 69 Months (Potential for Extension or Full-Time Conversion) Pay ...
Bend, OR · On-site
Title: CSV/CQV Specialist Position Summary: * Client is seeking a contractor-level CSV/CQV ... Partner with Quality Control, Instrumentation, Engineering, Automation, Quality Assurance, and ...
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Bend, OR · On-site
Title: CSV/CQV Specialist Position Summary: * Client is seeking a contractor-level CSV/CQV ... Partner with Quality Control, Instrumentation, Engineering, Automation, Quality Assurance, and ...
Bend, OR · On-site
AMTSOL is seeking a CSV/CQV Specialist to support high-priority qualification and validation ... Partner with QC, QA, Engineering, Automation, Instrumentation and system owners. * Manage ...
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Bend, OR · On-site
AMTSOL is seeking a CSV/CQV Specialist to support high-priority qualification and validation ... Partner with QC, QA, Engineering, Automation, Instrumentation and system owners. * Manage ...
$85 - $94.28/hr
The company is seeking a contractor-level CSV/CQV Specialist to support a high-priority backlog of ... Partner with Quality Control, Instrumentation, Engineering, Automation, Quality Assurance, and ...
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$85 - $94.28/hr
The company is seeking a contractor-level CSV/CQV Specialist to support a high-priority backlog of ... Partner with Quality Control, Instrumentation, Engineering, Automation, Quality Assurance, and ...
Drive computer system validation (CSV / CQV) activities in line with GAMP 5, US FDA 21 CFR Part 11 ... Mentor and develop engineers and coordinate across operations, quality, IT / OT and equipment ...
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Drive computer system validation (CSV / CQV) activities in line with GAMP 5, US FDA 21 CFR Part 11 ... Mentor and develop engineers and coordinate across operations, quality, IT / OT and equipment ...
Bend, OR · On-site
$80 - $85/hr
Drive computer system validation (CSV / CQV) activities in line with GAMP 5, US FDA 21 CFR Part 11 ... Mentor and develop engineers and coordinate across operations, quality, IT / OT and equipment ...
Quick apply
Bend, OR · On-site
$80 - $85/hr
Drive computer system validation (CSV / CQV) activities in line with GAMP 5, US FDA 21 CFR Part 11 ... Mentor and develop engineers and coordinate across operations, quality, IT / OT and equipment ...
Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...
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Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...
Portland, OR · On-site
$87K - $94K/yr
Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...
Portland, OR · On-site
$87K - $94K/yr
Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...
$87K - $94K/yr
Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...
$87K - $94K/yr
Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...
Job Title Validation - Engineer III / Lead Engineer - Project Farma Location(s) Customer Site - CA ... Perform CQV tasks, such as protocol development or equipment testing, under the Site Lead ...
Job Title Validation - Engineer III / Lead Engineer - Project Farma Location(s) Customer Site - CA ... Perform CQV tasks, such as protocol development or equipment testing, under the Site Lead ...
Bend, OR · On-site
$120 - $160/hr
Deep technical knowledge across diverse engineering disciplines--including process systems, automation architectures, instrumentation, and CSA (civil, structural, architectural) frameworks. CQV ...
Bend, OR · On-site
$120 - $160/hr
Deep technical knowledge across diverse engineering disciplines--including process systems, automation architectures, instrumentation, and CSA (civil, structural, architectural) frameworks. CQV ...
Deep technical knowledge across diverse engineering disciplines-including process systems, automation architectures, instrumentation, and CSA (civil, structural, architectural) frameworks. * CQV ...
Deep technical knowledge across diverse engineering disciplines-including process systems, automation architectures, instrumentation, and CSA (civil, structural, architectural) frameworks. * CQV ...
Deep technical knowledge across diverse engineering disciplines-including process systems, automation architectures, instrumentation, and CSA (civil, structural, architectural) frameworks. * CQV ...
Deep technical knowledge across diverse engineering disciplines-including process systems, automation architectures, instrumentation, and CSA (civil, structural, architectural) frameworks. * CQV ...
Job Title Validation - Engineer I / II - Project Farma Location(s) Customer Site - CA, Customer ... Perform CQV tasks, such as protocol development or equipment testing, under the Site Lead ...
Job Title Validation - Engineer I / II - Project Farma Location(s) Customer Site - CA, Customer ... Perform CQV tasks, such as protocol development or equipment testing, under the Site Lead ...
Bend, OR · On-site
The Senior Validation Engineer will be part of a cross functional team that will plan and execute ... Experience with designing CQV plans for Facilities, Utilities, and Process equipment desired
Bend, OR · On-site
The Senior Validation Engineer will be part of a cross functional team that will plan and execute ... Experience with designing CQV plans for Facilities, Utilities, and Process equipment desired
$34.9K - $45.4K
7% of jobs
$45.4K - $55.8K
2% of jobs
$55.8K - $66.3K
11% of jobs
$69.6K is the 25th percentile. Wages below this are outliers.
$66.3K - $76.8K
16% of jobs
$76.8K - $87.3K
14% of jobs
The median wage is $87.7K / yr.
$87.3K - $97.8K
14% of jobs
$97.8K - $108.2K
11% of jobs
$110.1K is the 75th percentile. Wages above this are outliers.
$108.2K - $118.7K
7% of jobs
$118.7K - $129.2K
12% of jobs
$129.2K - $139.7K
4% of jobs
$139.7K - $150.1K
3% of jobs
$34.9K
$94.3K
$150.1K
A CQV (Commissioning, Qualification, and Validation) Engineer is responsible for ensuring that equipment, systems, and processes within regulated industries, such as pharmaceuticals or biotechnology, meet regulatory and operational requirements. They develop and execute test protocols, troubleshoot issues, and document compliance with industry standards (e.g., FDA, GMP). Their role ensures that manufacturing facilities produce safe and effective products. CQV Engineers often collaborate with cross-functional teams, including quality, engineering, and operations.
To thrive as a CQV (Commissioning, Qualification, and Validation) Engineer, you need a solid background in engineering principles, GMP regulations, and life sciences or pharmaceutical processes, often supported by a relevant degree. Familiarity with quality management systems, risk assessment tools, and software for documentation and validation such as TrackWise or Veeva is commonly required, and certifications like Six Sigma or CQV-specific credentials are valuable. Strong analytical thinking, attention to detail, effective communication, and collaboration skills set top performers apart. These competencies are essential to ensure compliance, project success, and seamless interaction with cross-functional teams in highly regulated environments.
CQV Engineers in the pharmaceutical industry often encounter challenges such as managing strict timelines while ensuring full compliance with regulatory standards and adapting to evolving project requirements. They must coordinate with multiple departments including QA, production, and engineering to align project goals and documentation. Additionally, troubleshooting unexpected technical issues and staying updated with the latest industry guidelines can be demanding. However, overcoming these challenges is rewarding, as it directly contributes to the safe and effective delivery of life-saving products.
For Cqv Engineer jobs in Oregon, the most frequently searched job titles are:
The top searched job categories for Cqv Engineer jobs in Oregon are:

Bend, OR • On-site
8.3
Based on 42 frontline employees who took The Breakroom Quiz
26th of 86 rated pharmaceutical
People enjoy working here
Good employer
Paid breaks
Recommended by parents
Respectful managers
Full-time
Medical, Dental, Vision
Re-posted 22 days ago
CQV Engineer
Bend, OR
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 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.
Access to Lonza's global benefits program.
What you will do:
Partner with engineering, QA, and manufacturing teams to support smooth project execution.
Troubleshoot and improve equipment, processes, and systems.
Write, review, and execute qualification protocols (IQ/OQ/PQ) for new and existing equipment.
Identify risks to product quality and apply mitigation strategies.
Generate validation reports and maintain compliant documentation following FDA and cGMP guidelines.
Manage and close deviations or nonconformances identified during testing.
Support engineering documentation such as user requirements and design qualification materials.
What we are looking for:
High School Diploma or GED required; engineering degree preferred.
3-5 years of experience
Experience in CQV and temperature mapping.
Experience in Operational and Performance qualification testing
Understanding of FDA, ICH, ISPE, and ISO guidelines.
Proficiency with Microsoft Word and Excel.
Ability to solve problems and work crossfunctionally.
Strong communication and documentation skills.
Interest in improving systems and supporting safe, effective drug development.
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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Biotechnology research and development and pharmaceutical and medicine manufacturing
10,000+ Employees
Bern, KS, US