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Equipment Validation Manager Jobs (NOW HIRING)

ProKidney

Senior Manager, Validation

Winston Salem, NC · On-site

Position SummaryThe Sr. Manager of Validation will lead ProKidney's on-site Validation team ... Knowledge of pharmaceutical equipment, such as centrifuges, HVAC systems, building chillers, clean ...

Guerbet

Mgr Quality Validation

Raleigh, IL

Ensure all revalidation requirements are met for equipment, process, and cleaning site wide ... Manage validation activities for large scope capital projects (including Turnaround projects) that ...

sgsconsulting

Be Seen First

Commissioning Manager/ Validation Manager/CQV Manager

Chandler, AZ · On-site

$85 - $100/hr

... Validation, Equipment Vendors, and Project Management teams to ensure successful project delivery from Mechanical Completion through Operational Readiness. · Collaborate: Actively seeks out others ...

ZT Systems

Validation Lab Manager

Secaucus, NJ · On-site

$124K - $182K/yr

Maintain equipment and tools within the lab and ensure proper storage, including accurate ... validation and test experience * 0-2+ years managing technical teams. * Experience within a ...

ZT Systems

Validation Lab Manager

Georgetown, TX · On-site

Maintain equipment and tools within the lab and ensure proper storage, including accurate ... validation and test experience * 0-2+ years managing technical teams. * Experience within a ...

ProKidney

Senior Manager, Validation

Winston Salem, NC · On-site

Position Summary The Sr. Manager of Validation will lead ProKidney's on-site Validation team ... Knowledge of pharmaceutical equipment, such as centrifuges, HVAC systems, building chillers, clean ...

ZT Systems

Validation Lab Manager

Secaucus, NJ · On-site

$124K - $182K/yr

Maintain equipment and tools within the lab and ensure proper storage, including accurate ... validation and test experience * 0-2+ years managing technical teams. * Experience within a ...

ZT Systems

Validation Lab Manager

Georgetown, TX

Maintain equipment and tools within the lab and ensure proper storage, including accurate ... validation and test experience * 0-2+ years managing technical teams. * Experience within a ...

Forge Biologics

Validation Engineer I

Columbus, OH

Experience in equipment validation within a regulated industry. * Experience in qualifying a wide ... Strong project management skills, with the ability to prioritize and manage multiple validation ...

Forge Biologics

Validation Engineer I

Columbus, OH · On-site

Experience in equipment validation within a regulated industry. * Experience in qualifying a wide ... Strong project management skills, with the ability to prioritize and manage multiple validation ...

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Equipment Validation Manager information

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$47.5K

$105.4K

$160.5K

How much do equipment validation manager jobs pay per year?

As of Sep 14, 2026, the average yearly pay for equipment validation manager in the United States is $105,415.00, according to ZipRecruiter salary data. Most workers in this role earn between $74,500.00 and $132,000.00 per year, depending on experience, location, and employer.

What states have the most Equipment Validation Manager jobs?

States with the most job openings for Equipment Validation Manager jobs include:

What are popular job titles related to Equipment Validation Manager jobs?

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Infographic showing various Equipment Validation Manager job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 15% Part Time, 3% Contract, and 1% Nights. Highlights an 99% Physical, and 1% Remote job distribution, with an average salary of $105,415 per year, or $50.7 per hour.

Lead Engineer - Analytical Equipment Validation

Portsmouth, NH • On-site

Lonza
Biotechnology Research and Development • 10K+ employees
Learn more about Lonzaexternal

$104K - $137K/yr

Full-time

Retirement

Re-posted 15 days ago

Lonza rating

8.3

Company rating: 8.3 out of 10

Based on 42 frontline employees who took The Breakroom Quiz

Job description

Lead Engineer - Analytical Equipment Validation
Location: On-site, Portsmouth, NH. Relocation assistance is available for eligible candidates and their families, if needed.
The focus of the Computer Systems Validation (CSV)Lead Engineer role is to identify or create industry best practices and implement these within the framework of existing GAMP regulations. Responsibilities of the CSV Lead Engineer will include risk assessing systems, reviewing change requests and test scripts, drafting protocols and initiating and reviewing GMP documentation revisions as well as ownership of department procedures. The position provides guidance to junior team members.
What you will get:
  • A collaborative and inclusive work environment.
  • Opportunities for career growth and development.
  • Access to cutting-edge technologies and tools.
  • Competitive compensation and benefits package.
  • 401(k) matching plan.
  • Commitment to ethical and sustainable practices.

Our full list of global benefits can be found here: https://www.lonza.com/careers/benefits
What you will do:
  • Lead collaboration between internal teams and CSV to prioritize and complete activities on time.
  • Maintain knowledge of Lonza policies, 21 CFR Part 11, Data Integrity, ICH Q7A, and GAMP principles.
  • Perform QMS processes (Change Control, Deviation, CAPA) and validation maintenance of computerized systems.
  • Participate in audits and inspections as a Subject Matter Expert.
  • Own, revise and maintain CSV SOPs.
  • Support qualification activities and documentation for CSV validation in line with regulatory guidelines.
  • Function as CSV SME in inspections and Audits,

What we are looking for:
  • Bachelor's Degree is required (preferably in Computer Science/Software Engineering).
  • 5-10 years' of Computer Systems Validation experience.
  • Experience with 21 CFR Part 11 and ISPE GAMP guidelines as they relate to Computer Systems Validation .
  • Strong written and oral communication skills.
  • Strong organizational and time management 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.
Ready to shape the future of life sciences? Apply now.

What Lonza employees say

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About Lonza

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Industry

Biotechnology research and development and pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

Bern, KS, US

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