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Validation Department Jobs (NOW HIRING)

GL Staffing Services, Inc.

Validation

Boca Raton, FL · On-site

$75K - $95K/yr

Department: Quality Assurance Reports To: Senior Manager, Quality Assurance Employment Type ... Validation Master Plans (VMP) * User Requirement Specifications (URS) * Design Qualifications (DQ)

Unifin SAS

Validation Technician

Rochester, NY · On-site

Assists validation efforts in many ways including the following: executes/supports equipment ... Maintains department documentation in an orderly library so that information can be provided to ...

Unifin SAS

Validation Technician

Rochester, NY · On-site

Validation Technician Who we are? We are a French pharmaceutical industrial group, recognized for ... Library, maintains test equipment and department documentation. ESSENTIAL FUNCTIONS ...

Accupac

Validation Engineer

Lakewood, NJ

$77K - $95K/yr

Collaborate with clients, internal departments, and outside services to align on validation needs and timelines * Write and execute validation protocols and technical reports in compliance with cGMP ...

Chobani

Validation Specialist

Twin Falls, ID

Communicate any issues or concerns between other departments and the Sanitation Department. * Track/Report CIP validation progress on new and existing equipment. * Ensure compliance with all legal ...

Chobani

Validation Specialist

Twin Falls, ID · On-site

Communicate any issues or concerns between other departments and the Sanitation Department. * Track/Report CIP validation progress on new and existing equipment. * Ensure compliance with all legal ...

F.tech Inc.

Engineer, Validation

Chicago, IL · On-site

$70 - $95/hr

Evaluate validation requirements from automotive clients and develop adequate test methods and ... Make technical recommendations that positively affect the direction of a project and the department;

Herbalife

Engineer, Validation

Lake Forest, CA · On-site

Be able to work effectively with interdisciplinary departments to meet project deadlines and serve as a validation authority consulting with Engineering, Operations, and Quality. LEADERSHIP AND ...

Chobani

Validation Specialist

Twin Falls, ID · On-site

Communicate any issues or concerns between other departments and the Sanitation Department. * Track/Report CIP validation progress on new and existing equipment. * Ensure compliance with all legal ...

Chemtech Plastics, Inc.

Validation Engineer

Elgin, IL

$85K/yr

Validation Engineer 1st shift E-Verify Location: Elgin, IL | On-Site Job Summary: Leadership ... Work with Q.A. Dept. on piece part inspections and capability studies of new mold and engineering ...

Sigan America LLC

Validation Engineer

Ottawa, IL · On-site

$90K - $100K/yr

Senior Validation Engineer Location: Ottawa, Illinois Employment Type: Full-Time About the Position ... departments. This individual is organized, detail-oriented, and committed to maintaining the ...

Onsite Personnel LLC

Validation Engineer

Newtown, PA

Validation Engineer: Support site commissioning and qualification, which includes but is not ... Review all errors, protocol deviations, and comments with the respective user department Management ...

Herbalife

Engineer, Validation

Lake Forest, CA · On-site

Be able to work effectively with interdisciplinary departments to meet project deadlines and serve as a validation authority consulting with Engineering, Operations, and Quality. LEADERSHIP AND ...

voyant

Engineer, Validation

New Albany, OH

Support departments with technical insight on validation and compliance-related concerns. · Assist with environmental monitoring activities and interface with 3rd party labs. Review analytical and ...

Voyant Beauty

Engineer, Validation

New Albany, OH · On-site

Support departments with technical insight on validation and compliance-related concerns. • Assist with environmental monitoring activities and interface with 3rd party labs. Review analytical and ...

Herbalife

Engineer, Validation

Lake Forest, CA · On-site

Be able to work effectively with interdisciplinary departments to meet project deadlines and serve as a validation authority consulting with Engineering, Operations, and Quality. LEADERSHIP AND ...

Cryoport, Inc.

Validation Engineer

Irvine, CA · On-site

This is a client-facing role within the Cryoport Systems Consulting Services department that is ... Perform internal validations including developing validation protocols and reports, preparing ...

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All JobsValidation Department Jobs

Validation Department information

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How much do validation department jobs pay per hour?

As of Aug 23, 2026, the average hourly pay for validation department in the United States is $52.00, according to ZipRecruiter salary data. Most workers in this role earn between $39.42 and $63.22 per hour, depending on experience, location, and employer.

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

AspectValidation DepartmentQuality Assurance Specialist
CredentialsRelevant certifications like GxP, ISO, or industry-specific validation trainingCertifications such as ASQ CQE, Six Sigma, or ISO auditor
Work EnvironmentLaboratories, manufacturing plants, regulated industriesQuality departments, manufacturing facilities, service industries
Employer & Industry UsagePharmaceuticals, biotech, medical devices, regulated manufacturingManufacturing, healthcare, software, and service sectors
Common Search & ComparisonValidation DepartmentQuality Assurance Specialist

The Validation Department primarily focuses on qualifying and validating processes, equipment, and systems to ensure compliance with industry standards. Quality Assurance Specialists oversee overall quality processes, audits, and compliance. While both roles aim to ensure product quality and regulatory adherence, Validation Departments are more technical and process-specific, whereas Quality Assurance Specialists have a broader scope in quality management.

What does a validation department do?

A validation department is responsible for ensuring that processes, equipment, and systems meet specified standards and regulatory requirements. They develop and execute validation protocols, document results, and maintain compliance to ensure product quality and safety, often using tools like validation software and following industry guidelines such as GMP or ISO standards.

What is a validation department job?

A validation department job involves ensuring that processes, equipment, and systems meet specified standards and regulatory requirements. Roles typically include developing validation protocols, performing tests, and documenting results to confirm compliance, often requiring knowledge of Good Manufacturing Practices (GMP) and validation tools. These jobs are common in industries like pharmaceuticals, biotech, and manufacturing.
More about Validation Department jobs

What job categories do people searching Validation Department jobs look for?

The top searched job categories for Validation Department jobs are:

Infographic showing various Validation Department job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 16% Part Time, 3% Contract, and 1% Nights. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $108,152 per year, or $52 per hour.

Sr. Software Quality Engineer (Computer Software Validation-CSV)

MDAEdge

Jacksonville, FL • On-site

Full-time

Re-posted 29 days ago

Job description

Job Summary:
MDAEdge is a company focused on software quality in the medical device sector, and they are seeking a Senior Software Quality Engineer to lead Computer Software Validation (CSV) projects. The role involves managing software validation documentation, supporting compliance efforts, and promoting cross-functional collaboration within the organization.
Responsibilities:
• Lead Computer Software Validation (CSV) project planning activities, including the creation and updates of User Requirements Specifications (URS), Software Design Specifications (SDS), and Requirements Traceability Matrices (RTM).
• Develop, review, and approve software validation documentation.
• Create and execute qualification protocols, document reports, and review and approve software test scripts and code reviews.
• Evaluate and approve internal and vendor software packages and test documentation.
• Prioritize and manage all assigned projects within the software validation department.
• Implement and support policies, procedures, and processes related to CSV, Software Development Life Cycle (SDLC), and software validation for computerized systems.
• Serve as the Software Quality Engineering (SQE) representative in the Change Control Board (CCB) to facilitate change validation.
• Lead Installation Qualification (IQ) activities for manufacturing lines.
• Drive CSV improvement initiatives within the manufacturing environment.
• Promote cross-functional collaboration across different teams, sites, and operating companies in the area of CSV.
• Identify and resolve obstacles that impact business needs.
• Work closely with Franchise Quality to implement and sustain Quality System initiatives at the site level.
• Support compliance efforts by ensuring audit readiness and participating in internal and external audits related to CSV.
• Act as the Subject Matter Expert (SME) for CSV, leading investigations, responses, and remediation of site-specific CSV audit findings.
Qualifications:
Required:
• Strong working knowledge of FDA and European medical device regulations (QSR and ISO).
• Expertise in software validation requirements for both medical device production and Quality System software.
• Proficiency in GAMP5 and SDLC methodologies.
• In-depth understanding of regulations for electronic records, electronic signatures, and data integrity.
• Experience in change management with strong technical writing skills.
• Hands-on experience with SCADA and/or Manufacturing Execution Systems (MES), with a background in manufacturing/operations.
• Minimum of 4 years of experience in a regulated environment.
• 2-4 years of experience in medical device regulations.
• Strong knowledge of FDA and European medical device regulations (QSR and ISO).
• Expertise in software validation for medical device production and Quality System applications.
• Working knowledge of GAMP5 and SDLC.
• Understanding of electronic records, electronic signatures, and data integrity regulations.
• Experience with change management and technical writing.
• Hands-on experience with SCADA and/or MES in a manufacturing/operations setting.
Preferred:
• Medical device process validation experience.
• Experience in Quality Auditing and notified body inspections.
• Background in Quality Systems process development, support, integration, or enhancement.
• Experience in training or coaching others.
• Certification as a Software Quality Engineer (CSQE) or Quality Engineer (CQE).
Company:
The world doesn't have a talent shortage. It has a talent alignment problem. MDA Edge exists to fix that. Founded in , the company is headquartered in Sheridan, WY, US, , with a team of 51-200 employees. The company is currently Growth Stage.

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