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 ...
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 ...
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 ...
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 ...
Validation Project Managers
Burlington, MA · On-site
$78K - $98K/yr
The responsibilities of the Validation Project Manager include: 1) Manage multiple customer projects - including bacterial retention testing, physical testing (compatibility, product bubble point ...
Validation Project Managers
Burlington, MA · On-site
$78K - $98K/yr
The responsibilities of the Validation Project Manager include: 1) Manage multiple customer projects - including bacterial retention testing, physical testing (compatibility, product bubble point ...
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 ...
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 ...
Senior Validation Project Manager
Princeton, 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 ...
Quick apply
Senior Validation Project Manager
Princeton, 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 ...
Senior Validation Project Manager
$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 ...
Quick apply
Senior Validation Project Manager
$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 ...
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 ...
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 ...
Validation Project Managers
Burlington, MA · On-site
$78K - $98K/yr
The responsibilities of the Validation Project Manager include: 1) Manage multiple customer projects - including bacterial retention testing, physical testing (compatibility, product bubble point ...
Validation Project Managers
Burlington, MA · On-site
$78K - $98K/yr
The responsibilities of the Validation Project Manager include: 1) Manage multiple customer projects - including bacterial retention testing, physical testing (compatibility, product bubble point ...
Senior Validation Project Manager
Princeton, 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 ...
Senior Validation Project Manager
Princeton, 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 ...
Validation Project Lead
$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 ...
Quick apply
Validation Project Lead
$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 ...
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 ...
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 ...
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 ...
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 ...
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 ...
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 ...
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 ...
Quick apply
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 ...
This position requires experience with project management, good documentation practices, cGMP, & FDA validation methods and systems, ability to read engineering documents, set priorities, and work on ...
This position requires experience with project management, good documentation practices, cGMP, & FDA validation methods and systems, ability to read engineering documents, set priorities, and work on ...
This position requires experience with project management, good documentation practices, cGMP, & FDA validation methods and systems, ability to read engineering documents, set priorities, and work on ...
This position requires experience with project management, good documentation practices, cGMP, & FDA validation methods and systems, ability to read engineering documents, set priorities, and work on ...
This position requires experience with project management, good documentation practices, cGMP, & FDA validation methods and systems, ability to read engineering documents, set priorities, and work on ...
This position requires experience with project management, good documentation practices, cGMP, & FDA validation methods and systems, ability to read engineering documents, set priorities, and work on ...
Validation Lead
Brooklyn Park, MN · On-site +1
Lead and manage validation projects. This role coordinates, supports and assists all aspects of a computerized systems validation project from original concept through the final implementation.
Validation Lead
Brooklyn Park, MN · On-site +1
Lead and manage validation projects. This role coordinates, supports and assists all aspects of a computerized systems validation project from original concept through the final implementation.
Project Manager, Validation Who You'll Work With You will join one of our 45 offices in the US, be part of a committed team of over 1500 professionals, and work in teams and directly with our clients ...
Project Manager, Validation Who You'll Work With You will join one of our 45 offices in the US, be part of a committed team of over 1500 professionals, and work in teams and directly with our clients ...
Project Manager, Validation Who You'll Work With You will join one of our 45 offices in the US, be part of a committed team of over 1500 professionals, and work in teams and directly with our clients ...
Project Manager, Validation Who You'll Work With You will join one of our 45 offices in the US, be part of a committed team of over 1500 professionals, and work in teams and directly with our clients ...
Validation Project Manager information
See salary details
$47.5K - $57.8K
1% of jobs
$57.8K - $68K
4% of jobs
$76.6K is the 25th percentile. Wages below this are outliers.
$68K - $78.3K
24% of jobs
$78.3K - $88.6K
9% of jobs
The median wage is $96K / yr.
$88.6K - $98.9K
17% of jobs
$98.9K - $109.1K
8% of jobs
$109.1K - $119.4K
5% of jobs
$126.3K is the 75th percentile. Wages above this are outliers.
$119.4K - $129.7K
11% of jobs
$129.7K - $140K
8% of jobs
$140K - $150.2K
6% of jobs
$150.2K - $160.5K
8% of jobs
$47.5K
$105.4K
$160.5K
How much do validation project manager jobs pay per year?
As of Aug 4, 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.
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 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.
What is the difference between Validation Project Manager vs Quality Assurance Specialist?
| Aspect | Validation Project Manager | Quality Assurance Specialist |
|---|---|---|
| Certifications | GMP, ISO, PMP | ISO, Six Sigma, GMP |
| Work Environment | Regulated industries like pharma, biotech | Manufacturing, software, healthcare |
| Primary Focus | Ensuring validation processes and protocols | Maintaining quality standards and procedures |
| Employer Usage | Pharmaceutical, biotech, medical device companies | Manufacturers, 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:
Full-time
PTO
Re-posted 3 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.
As we continue to expand our presence in the Greater Philadelphia life sciences market, we are seeking an experienced Process & Validation Project Manager to lead capital projects, facility improvements, commissioning and qualification initiatives, and GMP manufacturing enhancements for our pharmaceutical and biotechnology clients.
This role offers the opportunity to work directly with industry-leading organizations while contributing to technically challenging projects that improve manufacturing performance, quality, and compliance.
At LAPORTE, we offer:
Responsibilities and Duties:
Qualifications:
Preferred Qualifications
Send us your application today. We look forward to meeting you!
The LAPORTE team
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.
As we continue to expand our presence in the Greater Philadelphia life sciences market, we are seeking an experienced Process & Validation Project Manager to lead capital projects, facility improvements, commissioning and qualification initiatives, and GMP manufacturing enhancements for our pharmaceutical and biotechnology clients.
This role offers the opportunity to work directly with industry-leading organizations while contributing to technically challenging projects that improve manufacturing performance, quality, and compliance.
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:
- Bachelor's degree in Engineering, Life Sciences, Construction Management, Project Management, or a related technical field.
- Minimum of 5 years of project management experience supporting pharmaceutical, biotechnology, medical device, or other regulated manufacturing environments.
- Demonstrated success managing engineering, facility, equipment installation, capital improvement, or operational excellence projects from initiation through closeout.
- Experience developing and maintaining project schedules, coordinating resources, tracking milestones, and driving projects to successful completion.
- Strong experience managing contractors, vendors, and cross-functional teams in a GMP-regulated environment.
- Proven ability to lead project meetings, communicate project status, and effectively manage stakeholder expectations at all organizational levels.
- Working knowledge of cGMP regulations and quality systems, including change management processes.
- Exceptional organizational, communication, problem-solving, and relationship management skills.
- Ability to manage multiple priorities and adapt to changing project requirements in a fast-paced environment.
- Willingness to travel to client sites as required.
Preferred Qualifications
- Experience overseeing facility renovations, equipment installations, utility upgrades, or manufacturing process improvement projects.
- Familiarity with project budgeting, forecasting, cost tracking, and resource planning.
- Experience coordinating activities across Engineering, Manufacturing, Quality Assurance, Validation, Maintenance, and Procurement teams.
- PMP certification or similar project management credential.
- Knowledge of commissioning, qualification, and validation processes within life sciences manufacturing environments.
- Experience working in aseptic processing, biotechnology, cell and gene therapy, or sterile manufacturing facilities.
- Familiarity with risk management methodologies and structured problem-solving tools.
Send us your application today. We look forward to meeting you!
The LAPORTE team