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Validation Project Manager Jobs (NOW HIRING)

CAI

Senior Validation Project Manager

Bridgewater, NJ

$102K - $111K/yr

We provide commissioning, qualification, validation, start-up, project management and other consulting services associated with operational readiness to FDA regulated and other mission-critical ...

CAI

Senior Validation Project Manager

Princeton, NJ

$102K - $111K/yr

We provide commissioning, qualification, validation, start-up, project management and other consulting services associated with operational readiness to FDA regulated and other mission-critical ...

CAI

Senior Validation Project Manager

Bridgewater, NJ

$102K - $111K/yr

We provide commissioning, qualification, validation, start-up, project management and other consulting services associated with operational readiness to FDA regulated and other mission-critical ...

CAI

Senior Validation Project Manager

Bridgewater, NJ · On-site

$102K - $111K/yr

We provide commissioning, qualification, validation, start-up, project management and other consulting services associated with operational readiness to FDA regulated and other mission-critical ...

CAI

Senior Validation Project Manager

Princeton, NJ

$102K - $111K/yr

We provide commissioning, qualification, validation, start-up, project management and other consulting services associated with operational readiness to FDA regulated and other mission-critical ...

Compli

Validation Project Lead

Broomfield, CO · On-site

$95K - $130K/yr

Validation Project Lead Location : Boulder, CO Compli, LLC was founded in 2001 to provide ... Manage changes to the project scope, project schedule and project costs using appropriate ...

GBA Companies

Validation Project Lead

Broomfield, CO · On-site

$95K - $130K/yr

Validation Project Lead Location : Boulder, CO Compli, LLC was founded in 2001 to provide ... Manage changes to the project scope, project schedule and project costs using appropriate ...

Compli

Validation Project Lead

Boulder, CO · On-site

$95K - $130K/yr

Validation Project Lead Location : Boulder, CO Compli, LLC was founded in 2001 to provide ... Manage changes to the project scope, project schedule and project costs using appropriate ...

Stellantis

Validation Project Chief

Auburn Hills, MI · On-site

Stellantis is seeking an EE Validation Project Chief (VPC) to lead and coordinate electrical system ... Manage manpower assessments, vehicle requests, test property readiness, vehicle program ...

Stellantis

Validation Project Chief

Auburn Hills, MI · On-site

Stellantis is seeking an EE Validation Project Chief (VPC) to lead and coordinate electrical system ... Manage manpower assessments, vehicle requests, test property readiness, vehicle program ...

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Validation Project Manager information

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$47.5K

$105.4K

$160.5K

How much do validation project manager jobs pay per year?

As of Jul 14, 2026, the average yearly pay for validation project 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 role of a validation manager?

A validation manager oversees the process of ensuring that manufacturing, laboratory, or quality systems meet regulatory standards and company requirements. They develop validation protocols, review validation activities, and ensure compliance with industry regulations such as GMP or ISO. Strong project management, documentation skills, and knowledge of validation tools are essential for this role.

How does a Validation Project Manager typically collaborate with cross-functional teams during a project?

A Validation Project Manager regularly collaborates with cross-functional teams such as quality assurance, regulatory affairs, engineering, and production to ensure that all validation activities meet regulatory standards and project timelines. This collaboration often involves coordinating meetings, aligning on project milestones, and facilitating clear communication to address any technical or compliance issues. Building strong working relationships across departments is crucial for anticipating challenges and ensuring a smooth validation process. Effective coordination helps to minimize delays and ensures that all documentation and testing requirements are thoroughly met.

What are the key skills and qualifications needed to thrive as a Validation Project Manager, and why are they important?

To thrive as a Validation Project Manager, you need expertise in regulatory compliance, project management, and validation protocols, often supported by a degree in engineering, life sciences, or a related field. Familiarity with validation software, quality management systems (QMS), and certifications like PMP or Six Sigma are commonly required. Exceptional organizational, leadership, and communication skills help coordinate cross-functional teams and manage complex timelines. These skills are crucial to ensure validated processes comply with industry standards, mitigate risks, and deliver successful project outcomes.

What are the 4 types of project managers?

The four main types of project managers are functional, projectized, matrix, and hybrid. Functional managers work within specific departments, projectized managers oversee entire projects independently, matrix managers operate across departments with shared authority, and hybrid combines elements of these structures. Understanding these types helps in selecting the right management approach for validation projects, which often require cross-functional coordination and compliance with industry standards.

What is a Validation Project Manager?

A Validation Project Manager is a professional responsible for overseeing and coordinating validation activities in industries such as pharmaceuticals, biotechnology, or manufacturing. Their main duties include ensuring that systems, equipment, and processes meet regulatory standards and operate as intended. They manage project timelines, resources, and communication among cross-functional teams to ensure successful validation outcomes. Additionally, they maintain documentation and ensure compliance with industry regulations such as FDA or GMP. This role is crucial for maintaining product quality, safety, and regulatory compliance.

How much does a validation manager make?

A validation project manager's salary typically ranges from $80,000 to $130,000 annually, depending on experience, industry, and location. They often hold certifications such as CQE or CSQE and work in regulated environments like pharmaceuticals or manufacturing, where validation skills are essential.

What type of project managers get paid the most?

Senior project managers, especially those in industries like IT, engineering, or finance, tend to earn the highest salaries. Project managers with specialized skills, certifications such as PMP, and extensive experience often command higher pay. Management roles overseeing large or complex projects also typically offer higher compensation.

What is the difference between Validation Project Manager vs Quality Assurance Specialist?

AspectValidation Project ManagerQuality Assurance Specialist
CertificationsGMP, ISO, PMPISO, Six Sigma, GMP
Work EnvironmentRegulated industries like pharma, biotechManufacturing, software, healthcare
Primary FocusEnsuring validation processes and protocolsMaintaining quality standards and procedures
Employer UsagePharmaceutical, biotech, medical device companiesManufacturers, software firms, healthcare providers

The Validation Project Manager primarily oversees validation activities, ensuring compliance with industry standards, while the Quality Assurance Specialist focuses on maintaining overall quality standards across processes. Both roles require similar certifications and are common in regulated industries, but their core responsibilities differ in scope and focus.

More about Validation Project Manager jobs
What cities are hiring for Validation Project Manager jobs? Cities with the most Validation Project Manager job openings:
What states have the most Validation Project Manager jobs? States with the most job openings for Validation Project Manager jobs include:
What job categories do people searching Validation Project Manager jobs look for? The top searched job categories for Validation Project Manager jobs are:
Validation Project Manager jobs near you
Infographic showing various Validation Project Manager job openings in the United States as of July 2026, with employment types broken down into 85% Full Time, 13% Part Time, 1% Temporary, and 1% Contract. Highlights an 86% Physical, 1% Hybrid, and 13% Remote job distribution, with an average salary of $105,415 per year, or $50.7 per hour.

Process & Validation Project Manager

LAPORTE L.C.C.

Philadelphia, PA • On-site

Full-time

PTO

Posted 14 days ago

Job description

Process & Validation Project Manager (a minimum of 5 years of experience required)
Location: Philadelphia, PA
Employment Type: Full-time, mostly onsite
About Us
Are you ready to take the next step in your career? LAPORTE, a consulting engineering firm with 25 years of experience and a strong presence in North America and Europe, is seeking an Process & Validation Project Manager to join our growing team. With 25 offices and over 480 employees worldwide, we specialize in delivering innovative solutions for the pharmaceutical and food & beverage industries.
The Process & Validation Project Manager is responsible for leading the coordination of projects of various systems across the pharmaceutical, biopharmaceutical, and medical device manufacturing sectors.
The Process & Validation Project Manager will live near Philadelphia, PA. They will be motivated to grow and excel with the support and direction from an interdisciplinary team of engineers. Become part of a supportive work environment that emphasizes team culture and empowering engineers with more responsibility, professional growth, and a work-life balance.
At LAPORTE, we offer:
  • Competitive Salary
  • Comprehensive Benefits
  • Compensatory Paid Time Off (PTO)
  • Paid Parental Leave
  • A Flexible Work Environment that values work-life balance
  • Opportunities for Professional Growth

Responsibilities and Duties:
  • Plan, coordinate, and execute facility improvement projects, including scope definition, scheduling, contractor coordination, and closeout documentation.
  • Serve as the primary on-site liaison for all project-related activities, ensuring minimal disruption to GMP operations and maintaining a safe working environment throughout project execution.
  • Initiate, author, and shepherd change control records through the site quality management system (QMS) in accordance with GMP change control procedures.
  • Coordinate and support the vendor approval and qualification process for new contractors and service providers, partnering with Procurement and QA as required.
  • Develop and maintain project schedules, status trackers, and progress reports for review by site leadership.
  • Identify and escalate project risks, scope changes, and schedule impacts in a timely manner, proposing mitigation strategies as appropriate.
  • Ensure all project activities comply with applicable GMP regulations, site SOPs, EHS requirements, and local building codes.

Qualifications:
  • Bachelors degree in engineering field or relevant equivalent.
  • Minimum 5 years of prior experience preparing and executing equipment qualification documents (IQ/OQ/PQ) required.
  • Excellent knowledge of the Current Good Manufacturing Practices.
  • Excellent communication skills - verbal, written, listening and interpersonal with the ability to transfer knowledge to others.
  • Strong technical knowledge, relationship management, organizational planning, and project management skills.
  • Ability to demonstrate a sense of urgency, flexibility, and accountability.
  • Flexibility to travel to the client site as required.

Preferred Qualifications
  • Prior experience performing GxP risk assessments such as Functional Risk Assessments (FRA) or Failure Mode and Effect Analysis (FMEA).
  • Experience in Aseptic Processing.
  • Familiarity with Computerized Systems Validation and ISPE GAMP5 and 21 CFR Part 11.

Send us your application today. We look forward to meeting you!
The LAPORTE team

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