ZipRecruiter

Log In

1

Quality Validation Manager Jobs (NOW HIRING)

Tolmar

Senior Quality Validation Engineer

Windsor, CO · On-site

$138K - $148K/yr

Lead risk assessments, develop risk management tools (e.g., FMEA, HACCP) and support change control ... validation data, prepare comprehensive reports, and ensure audit readiness. * Collaborate with QA, ...

Catapult

Senior Validation Manager

Princeton, NJ · On-site

Lead all validation activities in a hands-on approach and in collaboration with the engineering and Quality teams. * Manage multiple validation projects simultaneously, plan, coordinate and track the ...

Tolmar

Senior Quality Validation Engineer

Windsor, CO

$87K - $118K/yr

Lead risk assessments, develop risk management tools (e.g., FMEA, HACCP) and support change control ... validation data, prepare comprehensive reports, and ensure audit readiness. * Collaborate with QA, ...

Tolmar Inc.

Senior Quality Validation Engineer

Windsor, CO

$87K - $118K/yr

Lead risk assessments, develop risk management tools (e.g., FMEA, HACCP) and support change control ... validation data, prepare comprehensive reports, and ensure audit readiness. * Collaborate with QA, ...

General Motors

Applied ML Validation Manager

Sunnyvale, CA · On-site

$218K - $335K/yr

Role As an Applied ML Validation Manager on the Software Validation team within the AV organization ... Proven ability to define, implement, and track metrics that capture system quality, reliability ...

next page

Showing results 1-20

All JobsQuality Validation JobsQuality Validation Manager Jobs

Quality Validation Manager information

See salary details

$47.5K

$105.4K

$160.5K

How much do quality validation manager jobs pay per year?

As of Jul 22, 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 July 2026, with employment types broken down into 86% Full Time, 13% Part Time, and 1% Contract. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $105,415 per year, or $50.7 per hour.
NPI Quality/Validation Engineer

NPI Quality/Validation Engineer

Merrimack Manufacturing

Manchester, NH • On-site

$71K - $92K/yr

Full-time

Posted 16 days ago

Job description

Position Overview:
This position supports design transfer activities and quality operations in an innovative, fast-paced, medical device-manufacturing environment. This role includes generation and maintenance of control plans, risk management files, validation protocols, and other QMS documentation to support initial qualification and launch of commercial production activity. The role will also provide support to the organizational goals by leading improvement projects to increase efficiency and compliance across the site.
Responsibilities:
  • Leverage your engineering and technical experience to evaluate new products, manufacturing processes and ensure compliance with applicable regulatory standards throughout the New Product Introduction process
  • Provide input to the development, review, and update of User Requirements, critical quality attributes, and other design documentation
  • Lead project teams through validation protocol generation, execution, documentation organization, report writing, etc. while meeting schedule for final approval and release
  • Conduct investigations resulting in root cause and corrective actions through use of data analysis, inductive and deductive reasoning, and problem solving skills
  • Lead the evaluation and identification of validation requirements and sampling plans for new, and changes to, manufacturing processes, test methods, and equipment
  • Develop inspection procedures and sampling plans for new production, continuous improvement of process controls, and improved workflow/worker satisfaction
  • Assist in the development, implementation, and approval of Device Master Records, Device History Records, and Risk Management Files for new products
  • Provide guidance and assistance on the assessment of new and changes to existing manufacturing equipment, ensuring proper enrollment into QMS systems and that Validation requirements are met
  • Lead improvement projects to increase efficiency and compliance within Merrimack Manufacturing’s Quality Management System
  • Contain defective product and processes systemically, participate in Material Review Board (MRB) meetings, track and follow through with nonconformance investigations assigned to internal and external team members.
  • Support and contribute towards the success of external audits, whether conducted by the FDA, a Notified Body, other regulatory bodies, or external customers

Qualifications and Skills:
  • At least 3 years of experience in Medical Device Manufacturing or other similarly regulated industry such as Aerospace, Military, etc.
  • Strong knowledge of CFR Part 820 and ISO 13485 required
  • Lean or Six Sigma certification preferred
  • Strong knowledge of IQ/OQ/PQ requirements, measurement system analysis, and supporting engineering specifications
  • Knowledge of Design Transfer and introduction of new product processes and deliverables
  • Strong knowledge of tolerance stack up calculations and calibration best practices
  • Strong organization, communication, and time management skills; Project Management experience preferred
  • Knowledge of industry standards and best practices for Software Validation, Controlled Environments, Biocontamination Controls, and Gamma Irradiation also preferred

Education: B.A. or B.S. degree; equivalent experience in relevant technical fields will be considered

Powered by JazzHR

psg8kVNpPv