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Quality Validation Manager Jobs (NOW HIRING)

Machinify

Quality Validation Specialist

About the Opportunity The Quality Validation Specialist reviews completed outpatient coding ... Associate's or Bachelor's degree in Health Information Management, Healthcare Administration, or a ...

Bachem

Quality / Validation Engineer

Vista, CA · On-site

$103K - $142K/yr

A brief overview The Quality Engineer (QE) / Validation fulfills a critical role in GMP operations, supporting cleaning validation activities for API and PMO manufacturing, and the qualification of ...

Graphcore

Hardware Validation Manager

Austin, TX · On-site

... quality, and reliability targets before production release. Working closely with silicon, board ... Build, mentor, and manage a team of hardware validation engineers. * Collaborate with hardware ...

Graphcore

Hardware Validation Manager

Austin, TX · On-site

... quality products at scale. The Team Graphcore is a globally recognised leader in Artificial ... Build, mentor, and manage a team of hardware validation engineers. * Collaborate with hardware ...

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Quality Validation Manager information

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$47.5K

$105.4K

$160.5K

How much do quality validation manager jobs pay per year?

As of Jul 2, 2026, the average yearly pay for quality 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 is the difference between Quality Validation Manager vs Quality Assurance Specialist?

AspectQuality Validation ManagerQuality Assurance Specialist
CertificationsISO 9001, Six Sigma, CQEISO 9001, Six Sigma, CQE
Work EnvironmentManufacturing, pharmaceuticals, tech companiesManufacturing, healthcare, software development
ResponsibilitiesOversees validation processes, ensures compliance, manages validation teamsPerforms audits, develops QA procedures, monitors quality metrics

The main difference is that a Quality Validation Manager focuses on validating processes and systems to ensure compliance, often managing validation teams, while a Quality Assurance Specialist concentrates on implementing QA procedures, conducting audits, and maintaining quality standards. Both roles require similar certifications and are vital in industries like manufacturing and healthcare, but their core responsibilities differ in scope and focus.

More about Quality Validation Manager jobs
What cities are hiring for Quality Validation Manager jobs? Cities with the most Quality Validation Manager job openings:
What states have the most Quality Validation Manager jobs? States with the most job openings for Quality Validation Manager jobs include:
What job categories do people searching Quality Validation Manager jobs look for? The top searched job categories for Quality Validation Manager jobs are:
Quality Validation Manager jobs near you
Infographic showing various Quality Validation Manager job openings in the United States as of June 2026, with employment types broken down into 1% As Needed, and 99% Full Time. Highlights an 88% Physical, 4% Hybrid, and 8% Remote job distribution, with an average salary of $105,415 per year, or $50.7 per hour.
Validation Manager

Validation Manager

Thermo Fisher Scientific

Greenville, NC

Full-time

Posted 11 days ago

Thermo Fisher Scientific rating

7.8

Company rating: 7.8 out of 10

Based on 408 frontline employees who took The Breakroom Quiz

190th of 527 rated manufacturers

Job description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale...

About the Business
Join our Pharma Services Group (PSG)—a global leader providing integrated drug development and manufacturing solutions to pharmaceutical and biotech companies. Our Greenville, North Carolina site specializes in sterile and oral solid dose (OSD) manufacturing.

Discover Impactful Work
The Validation Manager (C&Q) will lead commissioning and qualification activities across the site, ensuring successful execution of capital projects and operational readiness.

A Day in the Life

  • Lead ~6 direct reports and ~25 contractors
  • Manage commissioning & qualification (C&Q) activities
  • Review and approve capital project requests
  • Allocate resources and manage workload across projects
  • Support equipment implementation and startup
  • Mentor team members and develop co-op pipeline
  • Collaborate cross-functionally across site functions

Keys to Success

Education

  • Bachelor’s degree in Engineering, Science, Chemistry, Biology, or related technical discipline

Experience

  • 6+ years of experience in commissioning, qualification, and/or validation within pharmaceutical or regulated manufacturing environments
  • Minimum 3+ years of leadership experience, including managing engineers and/or contractor teams
  • Hands-on experience supporting capital projects, including commissioning and qualification of new equipment and systems in a Steriles Manufacturing facility
  • Experience reviewing and approving technical project plans, validation strategies, and execution approaches
  • Proven ability to manage highly effective teams (FTEs + contractors) and a complex portfolio of concurrent projects
  • Experience collaborating cross-functionally with quality, process engineering, automation, facilities, maintenance, and operations
  • Experience supporting or developing early talent/co-op programs preferred

Knowledge, Skills, Abilities

  • Strong understanding of cGMP’s and C&Q processes
  • Project and resource management skills
  • Strong leadership and organizational capability

Competencies
Leadership, Project Management, Collaboration, Accountability, Operational Excellence

What Thermo Fisher Scientific employees say

Pay

Benefits

Hours and flexibility

Workplace

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