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 ...
Director of Capital Projects
Redmond, OR · On-site
Deep technical knowledge across diverse engineering disciplines--including process systems, automation architectures, instrumentation, and CSA (civil, structural, architectural) frameworks. * CQV ...
Director of Capital Projects
Redmond, OR · On-site
Deep technical knowledge across diverse engineering disciplines--including process systems, automation architectures, instrumentation, and CSA (civil, structural, architectural) frameworks. * CQV ...
Director of Capital Projects
Bend, OR · On-site
Deep technical knowledge across diverse engineering disciplines--including process systems, automation architectures, instrumentation, and CSA (civil, structural, architectural) frameworks. * CQV ...
Director of Capital Projects
Bend, OR · On-site
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 ...
Senior Validation Engineer
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
Senior Validation Engineer
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
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
Quick apply
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
Senior Validation Engineer
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
Senior Validation Engineer
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
Cqv Engineer information
See Oregon salary details
$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
How much do cqv engineer jobs pay per year?
What does a CQV engineer do?
How much do CQV engineers make in the US?
What is a CQV engineer?
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.
What are some common challenges faced by CQV engineers in the pharmaceutical industry?
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.
How much do CQV engineers make?
What are the key skills and qualifications needed to thrive as a CQV engineer?
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.

Full-time
Medical, Dental, Vision, PTO
Re-posted 27 days ago
Lonza rating
8.3
Based on 42 frontline employees who took The Breakroom Quiz
24th of 86 rated pharmaceutical
Job description
Director, Project Delivery (CAPEX Project Lead)
Location: Bend, OR, USA.
Note on Travel/Location: This role will be based full-time at our Bend, OR facility. Post-project, this role may transition to supporting other sites across the Americas region, with potential travel requirements scaling up to 50%.
We are seeking an elite, highly experienced engineering leader to join our Strategic Growth Investment Engineering (SGIE) team as the Director, Project Delivery (Project Lead). Reporting directly to the Senior Director, you will step into a high-visibility leadership role overseeing a $250MM + capital project portfolio. Operating under general direction, you will own the full project lifecycle from basic design through construction, commissioning, qualification, and startup (end of OQ). This role acts as a primary engineering anchor-leading multidisciplinary project teams, managing massive capital expense (CAPEX) allocations, and partnering with internal business units and global clients to deliver top-tier, compliant manufacturing facilities.
What will you get?
An agile career and dynamic working culture
An inclusive and ethical workplace
Compensation programs that recognize high performance
Medical, dental and vision insurance, as well as PTO and more
Our full list of global benefits can be found here: https://www.lonza.com/careers/benefits.
What you'll do:
Full-Lifecycle CAPEX Execution: Create, implement, and drive comprehensive project plans meeting explicit technical objectives across the Design, Construction, Commissioning, and Qualification (CQV) phases (through the end of OQ).
Multi-Million Dollar Budget Accountability: Directly manage complex capital asset budgets (CAR), ensure total adherence to financial forecasting, and ruthlessly oversee scope changes in partnership with GE Project Control.
Multidisciplinary Coordination: Lead, align, and coordinate the work of large, cross-functional project teams comprising Qualification Engineers, Facility Management, QA, Automation, and Black/Clean Utilities specialists.
Strategic Risk Mitigation: Proactively identify engineering and operational project risks, design robust mitigation strategies, and resolve complex roadblocks while balancing detail with the overall strategic picture.
Vendor & Procurement Management: Build and optimize long-term relationships with global contractors, equipment vendors, and architectural engineering firms to secure high-quality deliverables and strict timeline adherence.
Executive & Client Communication: Regularly communicate project status, milestone achievements, risks, and resource allocations to executive site leadership, global steering committees, and external commercial clients.
Safety, Quality, & Regulatory Compliance: Ensure all engineering aspects of the facility design build a highly compliant, cost-effective plant that strictly meets internal specifications, cGMP standards, and EHS regulations.
What we're looking for:
Experience: 10+ years of advanced project engineering and project management experience within the chemical, biochemical, or life sciences industries. Extensive experience executing large-scale capital projects within a Small Molecules or Advanced Synthetics environment is highly preferred.
Technical Mastery: Deep technical knowledge across diverse engineering disciplines-including process systems, automation architectures, instrumentation, and CSA (civil, structural, architectural) frameworks.
CQV & Startup Expertise: Proven track record utilizing modern Commissioning, Qualification, and Validation (CQV) strategies to minimize the time from construction completion to routine commercial production.
Leadership & Matrix Influence: Exceptional people management skills with a demonstrated ability to motivate, lead, and coach direct reports and multi-million dollar contingent workforces without relying on direct line authority.
Education: Bachelor's Degree is required. Skills and experience will be considered in additional to degree.
Soft Skills: Superior verbal and written communication skills (English fluency required, German capability is a plus) with the commercial acumen required to negotiate statement of work alterations and manage competing points of view.
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.
About Lonza
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