Validation Manager
Morrisville, PA · On-site
* You are able to manage the overall validation program for all operations and systems within the organization * Support multiple locations in executing validation protocols effectively * Interface ...
Morrisville, PA · On-site
* You are able to manage the overall validation program for all operations and systems within the organization * Support multiple locations in executing validation protocols effectively * Interface ...
Morrisville, PA · On-site
* You are able to manage the overall validation program for all operations and systems within the organization * Support multiple locations in executing validation protocols effectively * Interface ...
Morrisville, PA · On-site
* You are able to manage the overall validation program for all operations and systems within the organization * Support multiple locations in executing validation protocols effectively * Interface ...
Morrisville, PA · On-site
* You are able to manage the overall validation program for all operations and systems within the organization * Support multiple locations in executing validation protocols effectively * Interface ...
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 ...
Philadelphia, PA · On-site +1
Develop policies, procedures, standards, templates, and lifecycle management processes for validation activities. * Build a scalable validation framework consistent with current regulatory ...
Philadelphia, PA · On-site +1
Develop policies, procedures, standards, templates, and lifecycle management processes for validation activities. * Build a scalable validation framework consistent with current regulatory ...
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 ...
Philadelphia, PA · On-site +1
Develop policies, procedures, standards, templates, and lifecycle management processes for validation activities. * Build a scalable validation framework consistent with current regulatory ...
Philadelphia, PA · On-site +1
Develop policies, procedures, standards, templates, and lifecycle management processes for validation activities. * Build a scalable validation framework consistent with current regulatory ...
Philadelphia, PA · On-site +1
Develop policies, procedures, standards, templates, and lifecycle management processes for validation activities. * Build a scalable validation framework consistent with current regulatory ...
Philadelphia, PA · On-site +1
Develop policies, procedures, standards, templates, and lifecycle management processes for validation activities. * Build a scalable validation framework consistent with current regulatory ...
Pennington, NJ · On-site
$80K - $120K/yr
The position reports to the Sr. Validation Manager and is responsible for supporting commissioning, qualification, and validation (CQV) activities for GMP manufacturing facilities, utilities ...
Pennington, NJ · On-site
$80K - $120K/yr
The position reports to the Sr. Validation Manager and is responsible for supporting commissioning, qualification, and validation (CQV) activities for GMP manufacturing facilities, utilities ...
The Validation Specialist II helps manage the Software Validation Programs for Solesis Sister Companies Charter Medical LLC and Polyzen LLC to ensure compliance with FDA and current industry software ...
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The Validation Specialist II helps manage the Software Validation Programs for Solesis Sister Companies Charter Medical LLC and Polyzen LLC to ensure compliance with FDA and current industry software ...
Telford, PA · On-site
The Validation Specialist II helps manage the Software Validation Programs for Solesis Sister Companies Charter Medical LLC and Polyzen LLC to ensure compliance with FDA and current industry software ...
Telford, PA · On-site
The Validation Specialist II helps manage the Software Validation Programs for Solesis Sister Companies Charter Medical LLC and Polyzen LLC to ensure compliance with FDA and current industry software ...
The Validation Specialist II helps manage the Software Validation Programs for Solesis Sister Companies Charter Medical LLC and Polyzen LLC to ensure compliance with FDA and current industry software ...
The Validation Specialist II helps manage the Software Validation Programs for Solesis Sister Companies Charter Medical LLC and Polyzen LLC to ensure compliance with FDA and current industry software ...
Telford, PA · On-site
The Validation Specialist II helps manage the Software Validation Programs for Solesis Sister Companies Charter Medical LLC and Polyzen LLC to ensure compliance with FDA and current industry software ...
Telford, PA · On-site
The Validation Specialist II helps manage the Software Validation Programs for Solesis Sister Companies Charter Medical LLC and Polyzen LLC to ensure compliance with FDA and current industry software ...
Pennington, NJ · On-site
$80K - $120K/yr
The position reports to the Sr. Validation Manager and is responsible for supporting commissioning, qualification, and validation (CQV) activities for GMP manufacturing facilities, utilities ...
Pennington, NJ · On-site
$80K - $120K/yr
The position reports to the Sr. Validation Manager and is responsible for supporting commissioning, qualification, and validation (CQV) activities for GMP manufacturing facilities, utilities ...
$80K - $120K/yr
The position reports to the Sr. Validation Manager and is responsible for supporting commissioning, qualification, and validation (CQV) activities for GMP manufacturing facilities, utilities ...
$80K - $120K/yr
The position reports to the Sr. Validation Manager and is responsible for supporting commissioning, qualification, and validation (CQV) activities for GMP manufacturing facilities, utilities ...
Pennington, NJ · On-site
$90 - $120/hr
... Manager and is responsible for supporting commissioning, qualification, and validation (CQV) activities for GMP manufacturing facilities, utilities, equipment, computerized systems, and manufacturing ...
Pennington, NJ · On-site
$90 - $120/hr
... Manager and is responsible for supporting commissioning, qualification, and validation (CQV) activities for GMP manufacturing facilities, utilities, equipment, computerized systems, and manufacturing ...
Validate management interfaces such as CLI, APIs, gRPC, NETCONF, and SNMP, ensuring they operate reliably and meet design requirements. * Execute regression testing and support continuous integration ...
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Validate management interfaces such as CLI, APIs, gRPC, NETCONF, and SNMP, ensuring they operate reliably and meet design requirements. * Execute regression testing and support continuous integration ...
Newtown, PA · On-site
Manage responsibilities and workload to assure accurate and timely data and reports. * Initiate Change Controls in order to support validations in accordance with QMS processes. * Perform ...
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Newtown, PA · On-site
Manage responsibilities and workload to assure accurate and timely data and reports. * Initiate Change Controls in order to support validations in accordance with QMS processes. * Perform ...
Malvern, PA · On-site
Overview The Model Risk Management (MRM) Team, part of Vanguard's second line of defense, is ... In this role, you will perform independent validation and effective challenge of investment models ...
Malvern, PA · On-site
Overview The Model Risk Management (MRM) Team, part of Vanguard's second line of defense, is ... In this role, you will perform independent validation and effective challenge of investment models ...
Malvern, PA · On-site
Overview The Model Risk Management (MRM) Team, part of Vanguard's second line of defense, is ... In this role, you will perform independent validation and effective challenge of investment models ...
Malvern, PA · On-site
Overview The Model Risk Management (MRM) Team, part of Vanguard's second line of defense, is ... In this role, you will perform independent validation and effective challenge of investment models ...
Validation & ComplianceActivities: Assist basic and conceptual design phases of capital projects by ... Project Management & Leadership: Lead all aspects of client relationship development and project ...
Validation & ComplianceActivities: Assist basic and conceptual design phases of capital projects by ... Project Management & Leadership: Lead all aspects of client relationship development and project ...
$47.9K - $58.3K
1% of jobs
$58.3K - $68.7K
4% of jobs
$77.3K is the 25th percentile. Wages below this are outliers.
$68.7K - $79K
24% of jobs
$79K - $89.4K
9% of jobs
The median wage is $96.8K / yr.
$89.4K - $99.8K
17% of jobs
$99.8K - $110.1K
8% of jobs
$110.1K - $120.5K
5% of jobs
$127.5K is the 75th percentile. Wages above this are outliers.
$120.5K - $130.9K
11% of jobs
$130.9K - $141.2K
8% of jobs
$141.2K - $151.6K
6% of jobs
$151.6K - $162K
8% of jobs
$47.9K
$106.4K
$162K
A validation manager works in a manufacturing plant and oversees the proper operation of machinery and equipment. Your job duties include developing operational plans for the entire facility, identifying areas of process improvement, and scheduling periodic auditing reviews of the facility. The qualifications needed for a career as a validation manager include a bachelor’s degree in business, organizational theory, quality control, or a related field. You also need strong communication and computer skills and experience in a management position.
| Aspect | Validation Manager | Quality Assurance Specialist |
|---|---|---|
| Certifications | GxP, ISO, or industry-specific validation certifications | ISO, Six Sigma, or QA-related certifications |
| Work Environment | Regulated industries like pharmaceuticals, biotech, or medical devices | Manufacturing, software, or service industries |
| Primary Focus | Ensuring validation processes for equipment, systems, and processes meet standards | Monitoring and improving overall quality processes and compliance |
The Validation Manager primarily oversees validation activities to ensure compliance with industry standards, focusing on equipment and process validation. In contrast, the Quality Assurance Specialist concentrates on maintaining overall quality standards across products and services. Both roles are essential for compliance but differ in scope and responsibilities.
The most popular types of Validation jobs in Philadelphia, PA are:
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It services
11 - 50 Employees
Berkeley, CA, US
1989