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Senior Validation Specialist Jobs (NOW HIRING)

The Validation Specialist III is a senior-level professional responsible for leading the development, review, and execution of complex validation protocols supporting manufacturing, quality, and ...

The Validation Specialist III is a senior-level professional responsible for leading the development, review, and execution of complex validation protocols supporting manufacturing, quality, and ...

Validation Specialist - Utilities & Facilities Position Summary ... We are seeking two experienced Validation Engineers (mid-level to senior) with strong expertise in ...

Our client is seeking a Senior CSV Validation Specialist dedicated to Building Management System validation activities. This is an on-site role supporting a regulated pharmaceutical manufacturing ...

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Senior Validation Specialist information

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How much do senior validation specialist jobs pay per hour?

As of Aug 17, 2026, the average hourly pay for senior validation specialist in the United States is $50.45, according to ZipRecruiter salary data. Most workers in this role earn between $39.66 and $61.30 per hour, depending on experience, location, and employer.

What is a senior validation specialist?

Senior Validation Specialists are experienced professionals who ensure that processes, equipment, and systems in regulated industries—such as pharmaceuticals, biotechnology, and medical devices—meet quality and compliance standards. They develop, execute, and review validation protocols and reports to confirm that products are consistently produced and controlled according to established standards. These specialists also troubleshoot validation issues, oversee documentation, and often lead or mentor junior team members. Their work is critical for regulatory compliance and product safety.

What are the key skills and qualifications needed to thrive as a senior validation specialist?

To thrive as a Senior Validation Specialist, you need expertise in validation protocols, regulatory compliance (such as FDA or EMA requirements), and a strong background in life sciences or engineering, typically supported by a relevant degree. Familiarity with quality management systems (QMS), validation lifecycle documentation, and software tools like TrackWise or MasterControl is essential. Strong attention to detail, analytical thinking, and effective communication are vital soft skills in this role. These competencies ensure accurate validation processes, regulatory adherence, and the safe, efficient operation of products or systems.

What are some common challenges a senior validation specialist faces when managing multiple validation projects simultaneously?

A Senior Validation Specialist often oversees several projects at once, which can present challenges in prioritizing tasks, allocating resources, and ensuring that all documentation meets regulatory standards and deadlines. Balancing the demands of different stakeholders and coordinating cross-functional teams—such as QA, engineering, and production—requires strong organizational and communication skills. Staying updated with evolving regulatory requirements and addressing unexpected issues during validation testing are also common challenges that require adaptability and problem-solving abilities.

What is the difference between Senior Validation Specialist vs Validation Engineer?

AspectSenior Validation SpecialistValidation Engineer
Required CredentialsBachelor's degree, certifications in validation or quality assuranceBachelor's or master's in engineering, certifications in validation or quality assurance
Work EnvironmentPharmaceutical, biotech, or medical device industries, often in labs or manufacturingManufacturing, process development, or product testing in similar industries
Employer & Industry UsageUsed by pharmaceutical and biotech companies for compliance rolesCommonly employed in engineering and manufacturing sectors for process validation

While both roles focus on validation processes within regulated industries, the Senior Validation Specialist typically emphasizes overseeing validation activities, ensuring compliance, and leading validation projects. Validation Engineers often focus on designing, executing, and documenting validation protocols. The roles are complementary, with the Senior Validation Specialist having more experience and leadership responsibilities.

What cities are hiring for Senior Validation Specialist jobs?

Cities with the most Senior Validation Specialist job openings:

What are the most commonly searched types of Validation Specialist jobs?

The most popular types of Validation Specialist jobs are:

What states have the most Senior Validation Specialist jobs?

States with the most job openings for Senior Validation Specialist jobs include:

Infographic showing various Senior Validation Specialist job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 13% Part Time, and 3% Contract. Highlights an 90% Physical, 3% Hybrid, and 7% Remote job distribution, with an average salary of $104,945 per year, or $50.5 per hour.

Senior Validation Specialist

AllSTEM Connections

Rensselaer, NY • On-site

$114K/yr

Temporary

Medical, Dental, Vision, Retirement

Re-posted 27 days ago


Job description

Job Title: Senior Quality Validation Specialist
Role Overview
We are seeking a highly experienced Senior Quality Validation Specialist to provide technical leadership and quality oversight for validation activities within our highly regulated manufacturing facility. In this role, you will be responsible for the review and approval of validation protocols (IQ/OQ/PQ), change requests, and non-conformity investigations. You will serve as a subject matter expert during regulatory audits and inspections, ensuring that all equipment, systems, and processes maintain a constant state of validation and compliance. The ideal candidate is a proactive problem-solver with a deep understanding of root cause analysis and a commitment to continuous process improvement.
Key Responsibilities
• Validation Oversight: Provide quality review and approval for validation activities associated with system changes and site-wide projects. Ensure all activities align with local, corporate, and global regulatory standards.
• Protocol Management: Lead the preparation, execution, and data analysis for Installation, Operational, and Performance Qualification (IQ/OQ/PQ) protocols.
• Compliance & Technical Review: Perform rigorous technical reviews of protocol data and documentation. Identify process improvements before systems are placed under formal change control.
• Investigation & Root Cause Analysis: Review and approve validation failure investigations and non-conformities using advanced root cause analysis (RCA) techniques to ensure robust corrective actions.
• Audit & Inspection Support: Present and defend validation concepts, approaches, and documentation during internal audits and external regulatory inspections.
• Change Control: Manage the quality review and approval of Change Requests (CRs) to ensure the validated state of equipment and processes is maintained throughout their lifecycle.
• Annual Product Review (APR): Manage and complete assigned Annual Product Reviews, collaborating across departments to ensure data is compliant, sufficient, and delivered on time.
• Cross-Functional Collaboration: Serve as the validation liaison in engineering, R&D, and management meetings, communicating requirements and tracking documentation status across the facility.
Qualifications & Requirements
• Education & Experience:
• PhD in Chemistry, Engineering, or a relevant field with 4+ years of related work experience.
• MA/MS in Chemistry, Engineering, or a relevant field with 6+ years of related work experience.
• BA/BS in Chemistry, Engineering, or a relevant field with 8+ years of related work experience.
• Technical Mastery:
• Extensive experience in Validation/Quality disciplines within drug development or life sciences.
• Proven expertise in authoring and reviewing IQ/OQ/PQ protocols and reports.
• Strong command of Root Cause Analysis (RCA) and failure investigation methodologies.
• Communication: Ability to communicate complex validation requirements to personnel at all levels of the organization.
• Safety: Demonstrated commitment to safety awareness and safe work practices in a laboratory or manufacturing environment. Equal Opportunity Employer / Disabled / Protected Veterans
The Know Your Rights poster is available here:
https://www.eeoc.gov/sites/default/files/2023-06/22-088_EEOC_KnowYourRights6.12.pdf
The pay transparency policy is available here:
https://www.dol.gov/sites/dolgov/files/ofccp/pdf/pay-transp_%20English_formattedESQA508c.pdf
For temporary assignments lasting 13 weeks or longer, AllSTEM Connections is pleased to offer major medical, dental, vision, 401k and any statutory sick pay where required.
We are committed to working with and providing reasonable accommodations to individuals with disabilities. If you need a reasonable accommodation for any part of the employment process, please contact your staffing representative who will reach out to our HR team.
AllSTEM Connections participates in the E-Verify program in certain locations as required by law. Learn more about the E-Verify program.
https://e-verify.uscis.gov/web/media/resourcesContents/E-Verify_Participation_Poster_ES.pdf
We also consider for employment qualified applicants regardless of criminal histories, consistent with legal requirements, including, if applicable, the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance. Pursuant to applicable state and municipal Fair Chance Laws and Ordinances, we will consider for employment-qualified applicants with arrest and conviction records, including, if applicable, the San Francisco Fair Chance Ordinance. For Los Angeles, CA applicants: Qualified applications with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.
Additional Skills
(none specified)
AllSTEM Representative Contact Info
Account Executive:
Nichols
Branch Phone:
(909) 244-1777
Location:
Ontario, CA