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Method Validation Specialist Jobs (NOW HIRING)

The ideal candidate brings deep expertise in quality systems, validation methodologies, and regulatory frameworks, and thrives in a collaborative, cross-functional setting where precision ...

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Experience in applying risk-based methodologies for CSV/CSA * Experience in authoring validation deliverables (plans, specifications, test scripts, reports) and corresponding procedures * Familiarity ...

... based methodologies for CSV/CSAExperience in authoring validation deliverables (plans ... specifications, test scripts, reports) and corresponding proceduresFamiliarity with use of ...

Experience in applying risk-based methodologies for CSV/CSA * Experience in authoring validation deliverables (plans, specifications, test scripts, reports) and corresponding procedures * Familiarity ...

As a Coding Validation Specialist on the Complex Payment Solutions Team, you will play a critical ... Leveraging your expertise in coding guidelines, outpatient reimbursement methodologies, and ...

Senior Threat Validation Specialist

Helena, MT · On-site +1

$100K - $136K/yr

... Validation Specialist . This position is primarily responsible for vulnerability assessments ... Network traffic analysis methods. * Database, Cloud, and/or Web Application Security

Showing results 41-60

Method Validation Specialist information

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How much do method validation specialist jobs pay per hour?

As of Sep 15, 2026, the average hourly pay for method 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 are popular job titles related to Method Validation Specialist jobs?

For Method Validation Specialist jobs, the most frequently searched job titles are:

Senior Validation Specialist

On-site

Integrated Resources, Inc ( IRI )
Recruiting and Staffing Services • 51 - 200 employees

Other

Posted 2 days ago

New


Job description


  • We are seeking a highly skilled and experienced quality and validation professional to join a dynamic team within a fast-paced, regulated life sciences manufacturing environment.

  • This role is central to ensuring that all manufacturing processes, equipment, facilities, and systems meet the highest standards of quality, compliance, and regulatory integrity.

  • The ideal candidate brings deep expertise in quality systems, validation methodologies, and regulatory frameworks, and thrives in a collaborative, cross-functional setting where precision, accountability, and continuous improvement are paramount.


Qualifications & Experience:

  • Bachelor's degree in Engineering, Life Sciences, or a related technical discipline required; Master's degree preferred.

  • 6-9 years of experience in the pharmaceutical, biopharmaceutical, or other highly regulated manufacturing environments.

  • Strong background in quality validation, quality systems, and regulatory compliance within the life sciences industry.

  • Demonstrated experience leading and managing Corrective and Preventive Action (CAPA) investigations and activities.

  • Comprehensive knowledge of Quality System Regulations (QSR), GxP requirements, and industry best practices.

  • Experience supporting validation activities, including equipment, process, facility, computerized systems, and documentation review.

  • Preferred experience in high-speed aseptic filling operations and sterile manufacturing environments.

  • Proven ability to collaborate effectively with cross-functional teams, including Quality, Manufacturing, Engineering, Validation, and Regulatory Affairs.

  • Strong analytical and problem-solving skills with exceptional attention to detail.

  • Ability to manage multiple projects simultaneously while meeting aggressive timelines and strict deadlines.

  • Excellent verbal and written communication skills, with the ability to present complex information clearly to diverse stakeholders.

  • Self-motivated, organized, and capable of working independently in a fast-paced, regulated environment.

  • Quality Validation & Compliance

  • CAPA Management

  • Regulatory Knowledge (FDA, GMP, GxP, QSR)

  • Cross-Functional Collaboration

  • Project Management

  • Technical Documentation & Reporting

  • Continuous Improvement & Quality Excellence

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Integrated Resources logo

About Integrated Resources

Sourced by ZipRecruiter

Integrated Resources Inc (IRI), based in Edison, NJ, US, is an esteemed player in the staffing solutions industry with a credible presence on their official website irionline.com. Notably, IRI provides a range of professional staffing services including contract, contract-to-hire, and direct hire solutions to a wide spectrum of industries such as healthcare, life sciences, manufacturing, financial, insurance, and others. Since its inception, IRI has been committed to delivering top-talent and optimum solutions to meet its clients' diverse needs.

Industry

Recruiting and staffing services

Company size

51 - 200 Employees

Headquarters location

Edison, NJ, US

Year founded

1996