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Validation Manager Jobs (NOW HIRING)

Fresenius Kabi

Manager Validation

Wilson, NC · On-site

Manages the preparation and approval of validation protocols for critical equipment. * Reviews final documentation packages for all major validated systems at the plant including, but not limited to ...

Freseniusglobal

Manager Validation

Wilson, NC

Manages the preparation and approval of validation protocols for critical equipment. * Reviews final documentation packages for all major validated systems at the plant including, but not limited to ...

B. Braun Group

Verif and Validation Mgr

Goleta, CA · On-site

Braun Medical Inc., a leader in infusion therapy and pain management, develops, manufactures, and ... software validation testing, including software quality assurance. It is responsible for the ...

Rambus

Sr Mgr Validation Engineering

San Jose, CA · On-site

$161K - $300K/yr

The Validation Manager is a Full-Time position and the candidate will manage and cooperate with the team to validate and characterize the product to deliver high-quality buffer chip products. The ...

GSK

Validation Standards Manager

Hamilton, MT · On-site

Position Summary You will lead validation standards and provide technical expertise across a ... Certification or demonstrated experience in project management or risk management. * Experience ...

AMERICAN REGENT

Validation Sr. Manager

New Albany, OH · On-site

Essential Duties and Responsibilities Nothing in this restricts management's right to assign or reassign duties and responsibilities to this job at any time. Strategic Validation Leadership * Develop ...

MSD

Manager I, Validation

Rockville, MD · On-site

$101K - $154K/yr

The Manager I, Validation, is responsible for the development, implementation, and continuous improvement of the validation and calibration programs in compliance with applicable regulatory and ...

ZT Systems

Validation Lab Manager

Georgetown, TX

About the Role The Validation Lab Manager will manage a team of technicians supporting ZT System's Validation Engineering group on several projects in various stages of development. The Lab Manager ...

Truck Hero

Manager - Systems Validation

Ann Arbor, MI · On-site

POSITION SUMMARY The Manager of Systems Validation Engineering is responsible for the testing and validation function for RealTruck. This position will be responsible for leading the corporate ...

kindeva

Validation Engineer I

Saint Louis, MO

Primary responsible for protocol execution of various types of basic processing equipment under the direction of Validation Manger (For example (but not limited to) the following: cleaning (CIP &COP ...

ZT Systems

Validation Lab Manager

Secaucus, NJ · On-site

$124K - $182K/yr

About the Role The Validation Lab Manager will manage a team of technicians supporting ZT System's Validation Engineering group on several projects in various stages of development. The Lab Manager ...

Zoox

Manager, Firmware Validation

Foster City, CA · On-site

$198K - $249K/yr

Zoox is seeking an Engineering Manager to lead a verification and validation team with a focus on power and body systems on the robot in a variety of driving scenarios. In this role, you will lead a ...

kindeva

Validation Engineer I

Saint Louis, MO

Primary responsible for protocol execution of various types of basic processing equipment under the direction of Validation Manger (For example (but not limited to) the following: cleaning (CIP &COP ...

Cipla

$76K - $103K/yr

Site Engineering Manager Salary Range: $76,000 - $103,000 Duties and Responsibilities: • Design ... validation documentation and electrical schematics, installed equipment, installation or ...

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How much do validation manager jobs pay per year?

As of Jun 7, 2026, the average yearly pay for validation 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 Manager typically collaborate with other departments during project execution?

Validation Managers frequently work cross-functionally with quality assurance, manufacturing, engineering, and regulatory teams to ensure all systems and processes meet required standards. Effective collaboration involves coordinating validation protocols, sharing critical documentation, and communicating status updates to keep projects on track. A Validation Manager often leads meetings to align stakeholders, addresses compliance concerns, and resolves issues swiftly to prevent delays. Building strong relationships across departments is essential for smooth validation processes and successful project outcomes.

What is the role of a validation manager?

A validation manager oversees the process of ensuring that products, processes, or systems meet specified requirements and quality standards. They develop validation protocols, coordinate testing activities, and ensure compliance with industry regulations, often working with quality assurance teams and utilizing validation tools. Their role is critical in industries like pharmaceuticals, manufacturing, and healthcare to ensure safety and efficacy.

What Is a Validation Manager?

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.

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

To thrive as a Validation Manager, you need a strong background in quality assurance, regulatory compliance (such as FDA or EMA guidelines), and validation principles, usually supported by a degree in life sciences or engineering. Familiarity with validation protocols, risk management tools, and systems like GMP documentation platforms is essential. Leadership, attention to detail, and effective communication are crucial soft skills for managing teams and coordinating cross-functional projects. These skills and qualities ensure that products and processes consistently meet regulatory standards, reducing risks and ensuring compliance.

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

AspectValidation ManagerQuality Assurance Specialist
CertificationsGxP, ISO, or industry-specific validation certificationsISO, Six Sigma, or QA-related certifications
Work EnvironmentRegulated industries like pharmaceuticals, biotech, or medical devicesManufacturing, software, or service industries
Primary FocusEnsuring validation processes for equipment, systems, and processes meet standardsMonitoring 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.

What are Validation Managers?

Validation Managers are professionals responsible for overseeing and managing the validation processes within an organization, particularly in industries like pharmaceuticals, biotechnology, and manufacturing. Their main role is to ensure that products, equipment, and processes meet regulatory standards and operate consistently as intended. They coordinate validation activities, develop protocols, lead teams, and ensure compliance with quality and safety regulations. Validation Managers play a critical role in maintaining product quality, reducing risks, and ensuring that all procedures meet industry and governmental standards.
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Validation Manager jobs near you
Infographic showing various Validation Manager job openings in the United States as of May 2026, with employment types broken down into 1% As Needed, 98% Full Time, and 1% Contract. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $105,415 per year, or $50.7 per hour.

Manager Validation

Fresenius Kabi

Wilson, NC • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 22 days ago

Fresenius Kabi rating

8.3

Company rating: 8.3 out of 10

Based on 41 frontline employees who took The Breakroom Quiz

23rd of 71 rated pharmaceutical

Job description

Job Summary
Oversees the development and improvement of chemical and biological manufacturing processes for drugs and biological materials, while addressing issues related to the production scale-up and ensuring compliance with formulation specifications.
Salary Range: $90,816-$126,991
Position is eligible to participate in a bonus plan with a target of 10% of the base salary.
Final pay determinations will depend on various factors, including, but not limited to experience level, education, knowledge, skills, and abilities.
Our benefits and programs are comprehensive and thoughtfully crafted to ensure our colleagues live healthy lives and have support when it matters most. Benefits offered include a 401(k) plan with company contributions, paid vacation, holiday and personal days, employee assistance program, and health benefits to include medical, prescription drug, dental and vision coverage.
Responsibilities
  • The Manager/Team Leader oversees the following accountabilities in the assigned unit / department or team:
  • Developing new and improved processes for the economical, efficient, and safe chemical/biological manufacture of experimental and bulk active-drug/biological materials
  • Preparing large quantities of experimental drug/biological materials for extended analytical, pharmaceutical, biological, and clinical investigations
  • Reviewing and resolving issues involving the physical properties of a bulk product to ensure acceptability as required by formulation specifications
  • Making recommendations concerning acquisition and use of new technological equipment and materials
  • Manages the operational startup of major equipment and or processes by coordinating with Engineering, Operations, and Quality Control/Assurance Management.
  • Manages the preparation and approval of validation protocols for critical equipment.
  • Reviews final documentation packages for all major validated systems at the plant including, but not limited to utility systems, filling operations, packaging operations, dry heat sterilization/ depyrogenation, steam sterilizers and process washers.
  • Manages documentation required for regulatory submissions or responses as required, and assigns support for collection of information as needed.
  • Manages Coordination of qualification and re-qualification of manufacturing equipment. Review and approval of Protocols (Installation Qualification, Operational Qualification, Performance Qualifications) and final reports.
  • Responsible for preparation and updating of Validation Master Plan for Aseptic and Terminal Sterilization operation.
  • Manages project requirements with outside customers and vendors as required.
  • Responsible for evaluating/ troubleshooting equipment malfunctions and modifications as related to the Validation, and assigning change control requirements, where applicable.
  • Successful accomplishment of requalifications / periodic reviews of equipment according to site policies.
  • Successful validation (IQ, OQ, PQ) of all new equipment required to support plant operations.

REQUIREMENTS
  • Minimum 4-year degree in a Science or Engineering field of study or combination of education, experience, and training.
  • 5 + years of related experience in a cGMP facility
  • Installation, Operational and Performance Qualification protocol generation and execution
  • PC literate with standard office application (Word, Excel, PowerPoint, Project, Access) competency
  • Knowledge and understanding of cGMPs, industry guidance, and aseptic techniques
  • Understanding of statistical analysis tools and methods
  • Good communication skills and leadership skills are required.

Additional Information
We offer an excellent salary and benefits package including medical, dental and vision coverage, as well as life insurance, disability, 401K with company contribution, and wellness program.
Fresenius Kabi is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, citizenship, immigration status, disabilities, or protected veteran status.

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