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 ...
CQV Engineer - Periodic Review and Requalification Work Type: 100% Onsite Anticipated Start: Q1 2027 Initial Duration: Approximately 3-6 Months Schedule: Full-Time Employment Type: W2 Employee of ...
CQV Engineer - Periodic Review and Requalification Work Type: 100% Onsite Anticipated Start: Q1 2027 Initial Duration: Approximately 3-6 Months Schedule: Full-Time Employment Type: W2 Employee of ...
Senior Packaging CQV Engineer Summary: We are seeking a Senior CQV / Packaging Validation Engineer to lead qualification and validation activities for a new packaging line handling liquid products in ...
Senior Packaging CQV Engineer Summary: We are seeking a Senior CQV / Packaging Validation Engineer to lead qualification and validation activities for a new packaging line handling liquid products in ...
Senior Packaging CQV Engineer Summary: We are seeking a Senior CQV / Packaging Validation Engineer to lead qualification and validation activities for a new packaging line handling liquid products in ...
Quick apply
Senior Packaging CQV Engineer Summary: We are seeking a Senior CQV / Packaging Validation Engineer to lead qualification and validation activities for a new packaging line handling liquid products in ...
Thousand Oaks, CA · On-site
Pharmaceutical Senior CQV Engineer position is a direct hire which is expected to be on-site in Thousand Oaks, CA (Onsite). Summary We are seeking a highly motivated Senior CQV Engineer to support ...
Thousand Oaks, CA · On-site
Pharmaceutical Senior CQV Engineer position is a direct hire which is expected to be on-site in Thousand Oaks, CA (Onsite). Summary We are seeking a highly motivated Senior CQV Engineer to support ...
Bloomington, United States | Posted on 07/15/2026 CQV Engineer - Aseptic Filling Line and Isolator *This is a full-time opportunity with Pioneer GMP Consulting--not a position limited to a single ...
Bloomington, United States | Posted on 07/15/2026 CQV Engineer - Aseptic Filling Line and Isolator *This is a full-time opportunity with Pioneer GMP Consulting--not a position limited to a single ...
$100K - $130K/yr
Overview The CQV Engineer III position is an exciting opportunity to join PM Group's quickly growing Outsourced Technical Services(OTS) team near Oceanside, CA . Outsourced Technical Services (OTS ...
$100K - $130K/yr
Overview The CQV Engineer III position is an exciting opportunity to join PM Group's quickly growing Outsourced Technical Services(OTS) team near Oceanside, CA . Outsourced Technical Services (OTS ...
Senior Packaging CQV Engineer Summary: We are seeking a Senior CQV / Packaging Validation Engineer to lead qualification and validation activities for a new packaging line handling liquid products in ...
Senior Packaging CQV Engineer Summary: We are seeking a Senior CQV / Packaging Validation Engineer to lead qualification and validation activities for a new packaging line handling liquid products in ...
Syracuse, NY · On-site
$101K - $133K/yr
Role will drive the CQV strategy for the project, leading a team of engineers to successfully deliver deliverables * Author, edit, and execute technical commissioning, qualification and validation ...
Syracuse, NY · On-site
$101K - $133K/yr
Role will drive the CQV strategy for the project, leading a team of engineers to successfully deliver deliverables * Author, edit, and execute technical commissioning, qualification and validation ...
Oceanside, CA · On-site
$100K - $130K/yr
Overview The CQV Engineer III position is an exciting opportunity to join PM Group's quickly growing Outsourced Technical Services(OTS) team near Oceanside, CA . Outsourced Technical Services (OTS ...
Oceanside, CA · On-site
$100K - $130K/yr
Overview The CQV Engineer III position is an exciting opportunity to join PM Group's quickly growing Outsourced Technical Services(OTS) team near Oceanside, CA . Outsourced Technical Services (OTS ...
Senior Packaging CQV Engineer Summary: We are seeking a Senior CQV / Packaging Validation Engineer to lead qualification and validation activities for a new packaging line handling liquid products in ...
Senior Packaging CQV Engineer Summary: We are seeking a Senior CQV / Packaging Validation Engineer to lead qualification and validation activities for a new packaging line handling liquid products in ...
Senior Packaging CQV Engineer Summary: We are seeking a Senior CQV / Packaging Validation Engineer to lead qualification and validation activities for a new packaging line handling liquid products in ...
Senior Packaging CQV Engineer Summary: We are seeking a Senior CQV / Packaging Validation Engineer to lead qualification and validation activities for a new packaging line handling liquid products in ...
CQV Engineer - Commissioning, Qualification & Validation Location: Indianapolis, IN Travel: Up to 40% Domestic & International Travel Bring Critical Manufacturing Systems to Life PACIV stands for ...
CQV Engineer - Commissioning, Qualification & Validation Location: Indianapolis, IN Travel: Up to 40% Domestic & International Travel Bring Critical Manufacturing Systems to Life PACIV stands for ...
Lead and/or support the execution of CQV activities for facilities, utilities, manufacturing ... Work with Engineering, Quality, Operations, Automation, and vendors to coordinate commissioning and ...
Lead and/or support the execution of CQV activities for facilities, utilities, manufacturing ... Work with Engineering, Quality, Operations, Automation, and vendors to coordinate commissioning and ...
Chicago, IL · On-site
$70K - $100K/yr
Validation Engineer (CQV, GMP, Life Sciences) * Location: Greater Chicago * Salary: $70-100K + Bonus + Benefits * No Sponsorship, No Relocation Are you looking to build a career in validation ...
Chicago, IL · On-site
$70K - $100K/yr
Validation Engineer (CQV, GMP, Life Sciences) * Location: Greater Chicago * Salary: $70-100K + Bonus + Benefits * No Sponsorship, No Relocation Are you looking to build a career in validation ...
CQV Engineer - Commissioning, Qualification & Validation Location: Indianapolis, IN Travel: Up to 40% Domestic & International Travel Bring Critical Manufacturing Systems to Life PACIV stands for ...
CQV Engineer - Commissioning, Qualification & Validation Location: Indianapolis, IN Travel: Up to 40% Domestic & International Travel Bring Critical Manufacturing Systems to Life PACIV stands for ...
CQV Engineer (Commissioning, Qualification & Validation) Location: Indianapolis, IN Travel: Up to 40% domestic & international travel Bring Critical Manufacturing Systems to Life We bring advanced ...
CQV Engineer (Commissioning, Qualification & Validation) Location: Indianapolis, IN Travel: Up to 40% domestic & international travel Bring Critical Manufacturing Systems to Life We bring advanced ...
CQV Engineer - Commissioning, Qualification & Validation Location: Indianapolis, IN Travel: Up to 40% Domestic & International Travel Bring Critical Manufacturing Systems to Life PACIV stands for ...
Quick apply
CQV Engineer - Commissioning, Qualification & Validation Location: Indianapolis, IN Travel: Up to 40% Domestic & International Travel Bring Critical Manufacturing Systems to Life PACIV stands for ...
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 ...
$33K - $42.9K
7% of jobs
$42.9K - $52.8K
2% of jobs
$52.8K - $62.7K
11% of jobs
$65.9K is the 25th percentile. Wages below this are outliers.
$62.7K - $72.6K
16% of jobs
$72.6K - $82.5K
14% of jobs
The median wage is $82.9K / yr.
$82.5K - $92.5K
14% of jobs
$92.5K - $102.4K
11% of jobs
$104.1K is the 75th percentile. Wages above this are outliers.
$102.4K - $112.3K
7% of jobs
$112.3K - $122.2K
12% of jobs
$122.2K - $132.1K
4% of jobs
$132.1K - $142K
3% of jobs
$33K
$89.2K
$142K
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.
Cities with the most Cqv Engineer job openings:
States with the most job openings for Cqv Engineer jobs include:
For Cqv Engineer jobs, the most frequently searched job titles are:

Bend, OR • On-site
Full-time
Medical, Dental, Vision
Re-posted 3 days ago
8.3
Based on 42 frontline employees who took The Breakroom Quiz
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