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Validation Program Manager Jobs (NOW HIRING)

AMS Validation Manager

San Diego, CA · On-site

$225K - $338K/yr

... programs as one integrated validation organization. Success in this role requires developing a ... Manage multiple concurrent silicon programs by balancing technical execution, engineering ...

Validate that Epics are clearly defined and appropriately structured. * Ensure estimates are ... Program Management Required Experience Senior Associate Level Experience * 2-4 years of experience ...

New

Validate contract scope and deliverables with VA stakeholders, documenting any changes through formal change control processes * Manage assigned prime and subcontractor contracts Program Manager ...

As Senior Manager, Vehicle Validation, you will lead the team responsible for vehicle-level validation across Rivian's Stanton Springs North (SSN) programs. Your Program Leads own day-to-day ...

Through our expertise, insight, consulting and management skills, we accelerate breakthrough ... programs to make a career here truly life-enhancing. These recognitions are a testament to our ...

Senior Manager of Program Validation

Irvine, CA · On-site

$124K - $125K/yr

As Senior Manager, Vehicle Validation, you will lead the team responsible for vehicle-level validation across Rivian's Stanton Springs North (SSN) programs. Your Program Leads own day-to-day ...

If Program Manager sounds like something you would be interested in, and you meet the ... and validate large datasets effectively. · Excellent communication, teamwork, stakeholder ...

Coordinate APQP, PPAP, tooling development, engineering changes, validation activities, and ... Manage program documentation, change control activities, budgets, timing, and customer deliverables.

The Program Manager is responsible for the overall management and performance of the contract ... validate requirements, set priorities, and report project status. * Track and report program ...

Overview PROGRAM MANAGER (GCSS): Bowhead seeks a Program Manager to join our team in supporting the ... Essential functions to include - Validating technical and financial reports, analyze metrics ...

The Program Manager is responsible for the overall management and performance of the contract ... validate requirements, set priorities, and report project status. * Track and report program ...

The Program Manager is responsible for the overall management and performance of the contract ... validate requirements, set priorities, and report project status. * Track and report program ...

Program Manager

Washington, DC · On-site

$120K - $160K/yr

Analyze training assessments and customer feedback to validate or revise training investments, and present findings to surface training stakeholders. * Provide program management for navigation ...

Showing results 41-60

Validation Program Manager information

See salary details

$47.5K

$105.4K

$160.5K

How much do validation program manager jobs pay per year?

As of Sep 14, 2026, the average yearly pay for validation program 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 a validation program manager?

Validation Program Managers are professionals responsible for overseeing and coordinating the validation processes within an organization, particularly in industries like pharmaceuticals, biotechnology, and manufacturing. Their main role is to ensure that systems, equipment, and processes meet regulatory standards and perform consistently as intended. They manage validation projects, develop protocols, lead cross-functional teams, and ensure compliance with industry regulations such as FDA or ISO standards. By ensuring thorough validation, they help maintain product quality, safety, and regulatory compliance.

What are some typical challenges faced by a validation program manager when coordinating cross-functional teams?

A Validation Program Manager often navigates challenges such as aligning the priorities and timelines of cross-functional teams—including quality assurance, manufacturing, and regulatory affairs—to ensure validation activities progress smoothly. Communication gaps or differing departmental objectives can create bottlenecks, so proactive coordination and clear documentation are essential. Additionally, managing evolving regulatory requirements and adapting validation protocols accordingly requires both flexibility and attention to detail. Successfully overcoming these challenges not only supports project milestones but also strengthens stakeholder collaboration.

What are the key skills and qualifications needed to thrive as a validation program manager, and why are they important?

To thrive as a Validation Program Manager, you need expertise in validation protocols, regulatory compliance (such as FDA or EU GMP), and project management, often supported by a degree in engineering, life sciences, or a related field. Familiarity with validation lifecycle documentation tools, Quality Management Systems (QMS), and relevant industry certifications like Six Sigma or PMP is typically required. Strong leadership, attention to detail, and effective communication skills help coordinate teams and manage complex validation projects. These skills ensure validation processes meet regulatory standards, minimize compliance risks, and support successful product launches.

What is the difference between Validation Program Manager vs Validation Specialist?

AspectValidation Program ManagerValidation Specialist
CredentialsTypically requires a bachelor's degree in engineering, life sciences, or related field; certifications like CQE or CSQE are commonSimilar educational background; certifications like CQE or CSQE are also common
Work EnvironmentOversees validation projects across departments, manages teams, and ensures compliancePerforms hands-on validation tasks, executes validation protocols, and documents results
Employer & Industry UsageUsed in pharmaceutical, biotech, medical device, and manufacturing industriesCommonly found in similar industries, supporting validation activities

The Validation Program Manager focuses on overseeing validation projects, managing teams, and ensuring compliance at a program level. In contrast, the Validation Specialist handles the execution of validation protocols and detailed documentation. Both roles require similar credentials and are vital in regulated industries, but their responsibilities differ in scope and leadership level.

What cities are hiring for Validation Program Manager jobs?

Cities with the most Validation Program Manager job openings:

What states have the most Validation Program Manager jobs?

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

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

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

Senior Validation Engineer - Columbus, OH

Columbus, OH • On-site

Full-time

Medical, Retirement

Posted 5 days ago


Abbott rating

7.8

Company rating: 7.8 out of 10

Based on 139 frontline employees who took The Breakroom Quiz


Job description

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 122,000 colleagues serve people in more than 160 countries.
JOB DESCRIPTION:
Senior Validation Engineer
About Abbott
Abbott is a global healthcare leader, creating breakthrough science to improve people's health. We're always looking towards the future, anticipating changes in medical science and technology. Our nutrition business develops science-based nutrition products for people of all ages, from helping babies and children grow, to keeping adult bodies strong and active. Millions of people around the world count on our leading brands - including Similac®, PediaSure®, Pedialyte®, Ensure®, and Glucerna® - to help get the nutrients they need to live their healthiest life.
Working at Abbott
At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You'll also have access to:
  • Career development with an international company where you can grow the career you dream of.
  • Free medical coverage for employees* via the Health Investment Plan (HIP) PPO
  • An excellent retirement savings plan with high employer contribution
  • Tuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit - an affordable and convenient path to getting a bachelor's degree.
  • A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune.
  • A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists.
  • The stability of a company with a record of strong financial performance and history of being actively involved in local communities

WHAT YOU'LL DO:
As a Senior Validation Engineer, you will:
  • Manage Validation Program: Oversee the validation program for Strategic Capacity Expansions to ensure the success of large-scale capital projects.
  • Develop Validation Strategy: Create and align validation strategies for multi-million-dollar capital investments across all design phases.
  • Provide Guidance: Offer expertise on validation, design control strategies, and changes to products, processes, and equipment.
  • Team Management: Lead project validation and engineering teams (internal, external, VSPs) to ensure successful execution.
  • Monitor Progress: Develop metrics to track progress, adherence, and compliance of validation and design control processes; escalate issues as needed.
  • Navigate Challenges: Resolve conflicts between project execution and policy requirements to achieve compliant outcomes.
  • Support Resource Planning: Assist PM with validation resource planning, scheduling, and support structure.
  • Ensure Quality and Compliance: Support the development and delivery of quality, compliant documentation packages on time and cost-effectively.
  • Policy and Procedure Compliance: Ensure team adherence to policies, processes, and procedures for design control, process validation, and change control.
  • Cross-Functional Collaboration: Work with Technical, Engineering, Quality, and R&D to implement compliant product/process changes.
  • Education and Training: Provide visibility and training to ensure proper monitoring of CPPs and compliance with validation and design control regulations.
  • SME Role: Act as a Subject Matter Expert for validation, design control processes, statistical sampling plans, DOE, and FMEA.
  • Root Cause Analysis: Collaborate with the team to identify root causes of unexpected outcomes and develop compliant solutions.
  • Strategic Decision Making: Make strategic decisions for validation encompassing all project phases and resource allocation.
  • Leadership: Lead a team, ensuring adherence to the Abbott Code of Conduct and maintaining validation competency.
  • Documentation Oversight: Oversee review and approval of change processes, validation packages, and design control documentation.
  • Best Practices: Collaborate with corporate, divisional, and capacity expansion teams to utilize and improve validation and design control policies.
  • Budget Management: Manage the validation budget, ensuring spending within limits and supporting cost-efficient business processes.
  • Travel: 20-40% travel is expected as part of this role.

EDUCATION AND EXPERIENCE YOU'LL BRING:
Required:
  • Bachelor's degree in Life Science, Engineering, or closely related discipline is required.
  • 5+ years' experience in commissioning, qualification and validation (preferably with bulk liquid processing, aseptic processing, Clean-In-Place (CIP), evaporation, spray drying, dry blending, and/or powder handling unit operations in the food/pharma/nutrition industries).
  • Strong understanding of Good Documentation Practices (GDP), current Good Manufacturing Practices (cGMP) and 21 CFR Part 11. Familiarity with GAMP5 and FDA's Computer Software Assurance initiatives are preferred.
  • Proficient with Microsoft Word, Excel and Outlook for planning, reporting and collaborating.

Apply Now
Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: www.abbottbenefits.com
Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.
Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews and @AbbottGlobal.
The base pay for this position is
$78,000.00 - $156,000.00
In specific locations, the pay range may vary from the range posted.
JOB FAMILY:
Operations Quality
DIVISION:
ANSC Nutrition Supply Chain
LOCATION:
United States > Columbus : 2900 Easton Square Place
ADDITIONAL LOCATIONS:
WORK SHIFT:
Standard
TRAVEL:
Yes, 25 % of the Time
MEDICAL SURVEILLANCE:
No
SIGNIFICANT WORK ACTIVITIES:
Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day), Keyboard use (greater or equal to 50% of the workday)
Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.
EEO is the Law link - English: http://webstorage.abbott.com/common/External/EEO_English.pdf
EEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf

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