ZipRecruiter

Log In

1

Product Validation Manager Jobs (NOW HIRING)

GILLIG

Product Validation Engineer

Livermore, CA · Hybrid

Support the development and management or requirements along with the associated design verification (DV) and production validation (PV) plans, including traceability between requirements, test ...

Waymo

Validation Manager (Platforms)

San Diego, CA · On-site

Lead New Product Introduction (NPI) Validation Operations: Drive end-to-end program management for bringing new platform variants online in validation fleets, managing the critical path from vehicle ...

OMNIVISION

Product Validation Engineer

Santa Clara, CA · On-site

$120K - $125K/yr

Product Validation Engineer Job Duties: * Design a characterization/testing plan and work with R&D ... Proficiency in data analysis and visualization using Python and Excel to manage large datasets ...

YETI Coolers LLC

Product Validation Engineer

Austin, TX · On-site

About the Role The Product Validation Engineer plays a key role in the development of new products ... This role will partner closely with product management and Industrial design to understand the ...

RXinsider LTD.

Sr. Validation Manager

Bedford, OH · On-site

$92K - $158K/yr

Job Title Sr. Validation Manager Location Bedford, Ohio Job Type Full-time About Us As a developer ... Ensure processes and products are in compliance with all local, state, and federal rules and ...

Waymo

Validation Manager (Platforms)

Mountain View, CA · On-site

$190K - $234K/yr

Lead New Product Introduction (NPI) Validation Operations: Drive end-to-end program management for bringing new platform variants online in validation fleets, managing the critical path from vehicle ...

OMNIVISION

Product Validation Engineer

Santa Clara, CA

$120K - $125K/yr

Product Validation Engineer Job Duties: * Design a characterization/testing plan and work with R&D ... Proficiency in data analysis and visualization using Python and Excel to manage large datasets ...

Apple

AMS Validation Manager

San Diego, CA

$225K - $338K/yr

... products.","responsibilities":"- Lead and develop the San Diego AMS Silicon Validation team by ... Manage multiple concurrent silicon programs by balancing technical execution, engineering ...

YETI Coolers LLC

Product Validation Engineer

Austin, TX · On-site

About the Role The Product Validation Engineer plays a key role in the development of new products ... This role will partner closely with product management and Industrial design to understand the ...

Apple Inc.

AMS Validation Manager

San Diego, CA · On-site

... products. Responsibilities * - Lead and develop the San Diego AMS Silicon Validation team by ... Manage multiple concurrent silicon programs by balancing technical execution, engineering ...

previous pagenext page

Showing results 21-40

All JobsProduct Validation JobsProduct Validation Manager Jobs

Product Validation Manager information

See salary details

$51.5K

$159.4K

$197K

How much do product validation manager jobs pay per year?

As of Sep 10, 2026, the average yearly pay for product validation manager in the United States is $159,405.00, according to ZipRecruiter salary data. Most workers in this role earn between $141,000.00 and $197,000.00 per year, depending on experience, location, and employer.

What states have the most Product Validation Manager jobs?

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

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

For Product Validation Manager jobs, the most frequently searched job titles are:

Infographic showing various Product Validation Manager job openings in the United States as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 85% Physical, 2% Hybrid, and 13% Remote job distribution, with an average salary of $159,405 per year, or $76.6 per hour.

Product Process Validation Manager

Bridgeton, MO • On-site

kindeva
Pharmaceutical and Medicine Manufacturing
Learn more about kindevaexternal

Full-time

Re-posted 11 days ago

Key responsibilities

  • Lead the development, authorship, and execution of process validation strategies and PPQ protocols.

  • Serve as the MS&T lead for technology transfer activities, including developing transfer plans and process descriptions.

  • Partner with data analytics and quality teams to monitor process performance and lead investigations related to process deviations.

Kindeva rating

6.7

Company rating: 6.7 out of 10

Based on 9 frontline employees who took The Breakroom Quiz

Job description

Our Work Matters

At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world.

The Impact You Will Make

The is an exciting opportunity as Product Process Validation Manager is a key member of the Manufacturing Science & Technology (MS&T) organization, responsible for leading process validation strategy and execution across the product lifecycle. This role oversees the design, authorship, and facilitation of technology transfer activities, Process Performance Qualification (PPQ) protocols and reports, and supporting ongoing Continued Process Verification (CPV). The manager partners closely with Process Development, Quality, Manufacturing, and Regulatory Affairs to ensure robust, compliant, and efficient validation programs. This position reports directly to the Director of MS&T.

Role Responsibilities

Process Validation & PPQ

  • Lead the development, authorship, and execution of process validation strategies in alignment with regulatory expectations (e.g., FDA, EMA, ICH Q8–Q11).
  • Write, review, and approve PPQ protocols, sampling plans, risk assessments, and final reports.
  • Facilitate cross-functional PPQ readiness, including coordinating activities with Manufacturing, Quality Control, and Quality Assurance.
  • Ensure validation deliverables meet internal standards and external regulatory requirements.

Technology Transfer

  • Serve as the MS&T lead for technology transfer of new products, processes, or scale-up activities into manufacturing.
  • Develop and maintain tech transfer plans, process descriptions, and knowledge transfer documentation.
  • Drive process fit-gap assessments, risk analyses, and mitigation strategies.
  • Support equipment and facility readiness, including URS development and process capability assessments.

Continued Process Verification (CPV)

  • Partner with data analytics and quality teams to monitor process performance, identify trends, and drive data-based decision-making.
  • Lead investigations and corrective actions related to process performance deviations or CPV signals.

Cross-Functional Leadership

  • Collaborate with Process Development to translate laboratory-scale processes into robust, scalable manufacturing processes.
  • Support Regulatory Affairs with process validation content for submissions, responses to regulatory queries, and inspections.
  • Provide technical leadership during audits and regulatory inspections.
  • Mentor and guide junior MS&T staff in validation and tech transfer best practices.

Documentation & Compliance

  • Ensure all validation and tech transfer documentation is accurate, complete, and audit-ready.
  • Maintain strong alignment with internal quality systems, change control, and document management processes.
  • Champion continuous improvement initiatives to enhance validation efficiency and process robustness.

Basic Qualifications

  • Bachelor’s or Master’s degree in Engineering, Life Sciences, Biotechnology, or related field.
  • 7+ years of experience in biopharmaceutical or pharmaceutical manufacturing, MS&T, process validation, or related technical functions.
  • Demonstrated expertise in PPQ, CPV, and technology transfer.
  • Strong understanding of cGMP regulations and global validation guidelines.
  • Excellent technical writing, communication, and project management skills.

Preferred

  • Experience with biologics, cell therapy, gene therapy, or aseptic manufacturing.
  • Familiarity with statistical tools (e.g., JMP, Minitab) for process analysis.
  • Prior leadership or team management experience.
  • Experience supporting regulatory inspections.

#LI-Onsite

What Kindeva employees say

Pay

Hours and flexibility

Workplace

Get the full story on Breakroom

Apply