The QA Validation Specialist II will be responsible for providing QA oversight of regulated assets and business processes within the Validation Lifecycle Management System (VLMS), ensuring compliance ...
The QA Validation Specialist II will be responsible for providing QA oversight of regulated assets and business processes within the Validation Lifecycle Management System (VLMS), ensuring compliance ...
The QA Validation Specialist II will be responsible for providing QA oversight of regulated assets and business processes within the Validation Lifecycle Management System (VLMS), ensuring compliance ...
The QA Validation Specialist II will be responsible for providing QA oversight of regulated assets and business processes within the Validation Lifecycle Management System (VLMS), ensuring compliance ...
Sr QA Validation Specialist (Oversight)
Rensselaer, NY · On-site
$81K - $112K/yr
We are seeking a Sr. QA Validation Specialist to join our Quality Assurance team. As the Sr. QA Validation Specialist, you will support validation of equipment, utilities, software, cleaning and ...
Sr QA Validation Specialist (Oversight)
Rensselaer, NY · On-site
$81K - $112K/yr
We are seeking a Sr. QA Validation Specialist to join our Quality Assurance team. As the Sr. QA Validation Specialist, you will support validation of equipment, utilities, software, cleaning and ...
GMP QA Validation Specialist
Durham, NC · On-site
$45 - $53/hr
QA Validation Specialist Location: Research Triangle Park, NC - 27709 Duration: 10 Months Pay Rate: $45/hr - $53/hr on W2 The Validations Contractor - GMP Quality Assurance, reporting to the ...
GMP QA Validation Specialist
Durham, NC · On-site
$45 - $53/hr
QA Validation Specialist Location: Research Triangle Park, NC - 27709 Duration: 10 Months Pay Rate: $45/hr - $53/hr on W2 The Validations Contractor - GMP Quality Assurance, reporting to the ...
GMP QA Validation Specialist
Durham, NC · On-site
$45 - $53/hr
QA Validation Specialist Location: Research Triangle Park, NC - 27709 Duration: 10 Months Pay Rate: $45/hr - $53/hr on W2 The Validations Contractor - GMP Quality Assurance, reporting to the ...
GMP QA Validation Specialist
Durham, NC · On-site
$45 - $53/hr
QA Validation Specialist Location: Research Triangle Park, NC - 27709 Duration: 10 Months Pay Rate: $45/hr - $53/hr on W2 The Validations Contractor - GMP Quality Assurance, reporting to the ...
Quality Assurance Validation Specialist Position Summary Location: Thousand Oaks, California - On-site 40 Hours a week Assignment Duration: August 2026 through February 2027 Extension Potential: Yes ...
Quality Assurance Validation Specialist Position Summary Location: Thousand Oaks, California - On-site 40 Hours a week Assignment Duration: August 2026 through February 2027 Extension Potential: Yes ...
Quality Assurance Validation Engineer
Thousand Oaks, CA · On-site
$110 - $180/hr
Intermediate, with 6+ years of experience We are seeking an experienced Quality Assurance Validation Specialist to provide quality oversight for pharmaceutical and biopharmaceutical validation ...
New
Quality Assurance Validation Engineer
Thousand Oaks, CA · On-site
$110 - $180/hr
Intermediate, with 6+ years of experience We are seeking an experienced Quality Assurance Validation Specialist to provide quality oversight for pharmaceutical and biopharmaceutical validation ...
New
Intermmediate, with 6+ years of relevant experience We are seeking an experienced Quality Assurance Validation Specialist to provide quality oversight for pharmaceutical and biopharmaceutical ...
Quick apply
Intermmediate, with 6+ years of relevant experience We are seeking an experienced Quality Assurance Validation Specialist to provide quality oversight for pharmaceutical and biopharmaceutical ...
Specialist, Quality Assurance Validation
$96K - $120K/yr
The Quality Assurance Specialist provides QA oversight for Facility, Equipment, Utility (FEU), and ... Commissioning, Qualification, and Validation * Provide QA compliance oversight for Facility ...
Quick apply
Specialist, Quality Assurance Validation
$96K - $120K/yr
The Quality Assurance Specialist provides QA oversight for Facility, Equipment, Utility (FEU), and ... Commissioning, Qualification, and Validation * Provide QA compliance oversight for Facility ...
Specialist, Quality Assurance Validation
Bothell, WA · On-site
$96K - $120K/yr
The Quality Assurance Specialist provides QA oversight for Facility, Equipment, Utility (FEU), and ... Commissioning, Qualification, and Validation * Provide QA compliance oversight for Facility ...
Specialist, Quality Assurance Validation
Bothell, WA · On-site
$96K - $120K/yr
The Quality Assurance Specialist provides QA oversight for Facility, Equipment, Utility (FEU), and ... Commissioning, Qualification, and Validation * Provide QA compliance oversight for Facility ...
Specialist, Quality Assurance Validation
Bothell, WA · On-site
$96K - $120K/yr
The Quality Assurance Specialist provides QA oversight for Facility, Equipment, Utility (FEU), and ... Commissioning, Qualification, and Validation * Provide QA compliance oversight for Facility ...
Specialist, Quality Assurance Validation
Bothell, WA · On-site
$96K - $120K/yr
The Quality Assurance Specialist provides QA oversight for Facility, Equipment, Utility (FEU), and ... Commissioning, Qualification, and Validation * Provide QA compliance oversight for Facility ...
Specialist, QA Validation & EngineeringAbout Site Catalent's Baltimore site is a leading facility specializing in biologics development and manufacturing, offering state-of-the-art capabilities for ...
Specialist, QA Validation & EngineeringAbout Site Catalent's Baltimore site is a leading facility specializing in biologics development and manufacturing, offering state-of-the-art capabilities for ...
The Validation Specialist is responsible for planning, coordinating, and executing all ... Prepare summary reports for Quality Assurance approval. Cross-functional Collaboration:
The Validation Specialist is responsible for planning, coordinating, and executing all ... Prepare summary reports for Quality Assurance approval. Cross-functional Collaboration:
The Validation Specialist is responsible for planning, coordinating, and executing all ... Prepare summary reports for Quality Assurance approval. Cross-functional Collaboration:
The Validation Specialist is responsible for planning, coordinating, and executing all ... Prepare summary reports for Quality Assurance approval. Cross-functional Collaboration:
The Validation Specialist is responsible for planning, coordinating, and executing all ... Prepare summary reports for Quality Assurance approval. Cross-functional Collaboration:
New
The Validation Specialist is responsible for planning, coordinating, and executing all ... Prepare summary reports for Quality Assurance approval. Cross-functional Collaboration:
New
The Validation Specialist is responsible for planning, coordinating, and executing all ... Prepare summary reports for Quality Assurance approval. Cross-functional Collaboration:
The Validation Specialist is responsible for planning, coordinating, and executing all ... Prepare summary reports for Quality Assurance approval. Cross-functional Collaboration:
The Validation Specialist is responsible for planning, coordinating, and executing all ... Prepare summary reports for Quality Assurance approval. Cross-functional Collaboration:
The Validation Specialist is responsible for planning, coordinating, and executing all ... Prepare summary reports for Quality Assurance approval. Cross-functional Collaboration:
The Validation Specialist is responsible for planning, coordinating, and executing all ... Prepare summary reports for Quality Assurance approval. Cross-functional Collaboration:
The Validation Specialist is responsible for planning, coordinating, and executing all ... Prepare summary reports for Quality Assurance approval. Cross-functional Collaboration:
Validation Specialist (Cleaning-In-Place)
Humacao, PR · On-site
$80 - $100/hr
Validation Specialist (Cleaning-In-Place) Validation & Engineering Group, Inc. (V&EG) a Pinnaql ... Prepare summary reports for Quality Assurance approval. Cross-functional Collaboration
New
Validation Specialist (Cleaning-In-Place)
Humacao, PR · On-site
$80 - $100/hr
Validation Specialist (Cleaning-In-Place) Validation & Engineering Group, Inc. (V&EG) a Pinnaql ... Prepare summary reports for Quality Assurance approval. Cross-functional Collaboration
New
Validation Specialist (Cleaning-In-Place)
Humacao, PR · On-site
$80 - $120/hr
Validation Specialist (Cleaning-In-Place) Validation & Engineering Group, Inc. (V&EG) a Pinnaql ... Prepare summary reports for Quality Assurance approval. Cross-functional Collaboration
New
Validation Specialist (Cleaning-In-Place)
Humacao, PR · On-site
$80 - $120/hr
Validation Specialist (Cleaning-In-Place) Validation & Engineering Group, Inc. (V&EG) a Pinnaql ... Prepare summary reports for Quality Assurance approval. Cross-functional Collaboration
New
Qa Validation Specialist information
See salary details
$15.87 - $21.28
3% of jobs
$21.28 - $26.70
3% of jobs
$26.70 - $32.12
3% of jobs
$32.12 - $37.54
8% of jobs
$39.98 is the 25th percentile. Wages below this are outliers.
$37.54 - $42.96
16% of jobs
$42.96 - $48.38
9% of jobs
The median wage is $50.58 / hr.
$48.38 - $53.80
17% of jobs
$58.95 is the 75th percentile. Wages above this are outliers.
$53.80 - $59.22
16% of jobs
$59.22 - $64.64
8% of jobs
$64.64 - $70.06
7% of jobs
$70.06 - $75.48
8% of jobs
$15
$50
$75
How much do qa validation specialist jobs pay per hour?
What is a QA Validation Specialist?
How does a QA Validation Specialist typically collaborate with other departments during the product development lifecycle?
What are the key skills and qualifications needed to thrive as a QA Validation Specialist, and why are they important?
What is the difference between Qa Validation Specialist vs Quality Assurance Analyst?
| Aspect | Qa Validation Specialist | Quality Assurance Analyst |
|---|---|---|
| Certifications | GxP, ISO, or industry-specific validation certifications | ISO, Six Sigma, or general QA certifications |
| Work Environment | Regulated industries like pharmaceuticals, biotech, medical devices | Various industries including manufacturing, software, healthcare |
| Employer Usage | Companies requiring validation of systems/equipment | Organizations focusing on process and product quality |
Qa Validation Specialists focus on validating systems and equipment to meet regulatory standards, primarily in regulated industries. Quality Assurance Analysts oversee overall quality processes, often across diverse sectors. While both roles ensure quality, the Validation Specialist emphasizes compliance and validation protocols, whereas the Analyst concentrates on process improvement and defect prevention.
What cities are hiring for Qa Validation Specialist jobs?
Cities with the most Qa Validation Specialist job openings:
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The top searched job categories for Qa Validation Specialist jobs are:

Full-time
Medical, Dental, Vision, Retirement
Posted 5 days ago
Job description
Join Immatics and shape the future of cancer immunotherapy; one patient at a time!
Immatics is committed to making a meaningful impact on the lives of patients with cancer. We are the global leader in precision targeting of PRAME, a target expressed in more than 50 cancers. Our cutting-edge science and robust clinical pipeline form the broadest PRAME franchise with the most PRAME indications and modalities, spanning TCR T-cell therapies and TCR bispecifics.
Why Join Us?
Innovative Environment: Help to pioneer advancements in cancer immunotherapy.
Collaborative Culture: Be part of a diverse team dedicated to your professional growth.
Global Impact: Contribute to therapies that make a lasting impact on patients globally.
Role Overview
We are seeking a Quality Assurance Validation Specialist II to support our Global Quality Operations team. The QA Validation Specialist II will be responsible for providing QA oversight of regulated assets and business processes within the Validation Lifecycle Management System (VLMS), ensuring compliance with the Quality Management System (QMS) and GMP requirements. This role will also serve as a Subject Matter Expert (SME) in biopharmaceutical quality and as an on-site QA representative within the U.S. QA Validation team.
Schedule: 8:00 AM - 5:00 PM; Monday to Friday; On-site
Reports to: Senior Manager, Quality Assurance Validation
Location: 13203 Murphy Road Suite 100 Stafford, TX 77477
Basic Qualifications:
Bachelor Degree in Engineering, Life Sciences, Computer Science or related.
At least three years' experience in a related role.
Possess scientific, technical background with experience in Biotechnology, Engineering, Computer Science or related field as well as work experience in related Biopharma industry or similar regulated settings.
Advanced understanding of Validation Lifecycle Pillars, which may include equipment lifecycle management, equipment qualification execution, equipment operation, equipment maintenance, workflows incl. GxP Computerized System Validation (CSV), Qualification phases such as IQ, OQ, PQ, Manufacturing Process Validation and Continued Process Verification.
Preferred Qualifications: Experience in one or more of the following areas:
Quality Assurance (QA) validation within a regulated biopharmaceutical environment.
QA release activities within regulated environments.
Regulatory audits and inspections.
Development, review, and contribution to documentation supporting the testing, validation, and release of Quality Control (QC) and production equipment within clinical and/or commercial GMP environments.
Cell and Gene Therapy operations, including clinical and/or commercial-stage environments.
Software application deployment, administration, and periodic review within regulated environments.
Analytical method validation.
In this role you will:
Review and approve asset validation documentation, including User Requirement Specifications (URS), Risk Assessments, Validation Plans, Qualification Protocols, and Validation Reports.
Review and approve operational, maintenance, and cleaning (OMC) procedures, ensuring compliance with quality requirements and Good Documentation Practices (GDP).
Ensure compliance with applicable regulations and the company's Quality Management System (QMS).
Serve as the QA representative for validation deliverables related to GxP-regulated computerized systems, production equipment, laboratory methods, facilities, and IT infrastructure.
Provide QA guidance and best practices based on industry standards and current Cell Therapy practices, including Adoptive Cell Therapy.
Collaborate with cross-functional stakeholders to align QA Validation activities with U.S. QA Validation Management, Global Quality Operations, and Site Leadership.
Provide QA support for Data Management, Digitalization, Artificial Intelligence (AI), Operational Excellence, Business Continuity, and Archival initiatives.
What do we offer?
At Immatics, we believe in investing in our team's health, safety and well-being. Here's what you can expect if you join Immatics
Comprehensive Benefits:
Competitive rates for Health, Dental, and Vision Insurance
4 weeks of vacation, granted up front each year and prorated for first and last year of employment.
12 company paid holidays
7 days of sick time
100% employer-paid life insuranceup to at 1x annual salary, up to one hundred thousand dollars
100% employer-paid short- and long-Term disability coverage
401(k) with immediate eligibilityand company match...
The company will match 100% of your contributions up to 3% of your base salary for the first two years of employment, 4% for years 2-3 of employment, and up to 5% of your salary from the fourth year onward of continued employment.
Partially paid parental leavefor eligible employees.
Additional voluntary employee-paid benefits and services, including accident, hospital indemnity, and critical illness insurance, as well as identity theft protection and pet insurance.
Equal Employment Opportunity
We are an equal opportunity employer and are committed to building a diverse and inclusive workplace. We consider all qualified applicants for employment without regard torace, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexualorientation, gender identity or expression, national origin, ancestry, age, marital status, disability, geneticinformation, veteran status, or any other status protected by applicable law.
Reasonable Accommodations
We are committed to providing reasonable accommodations to individuals with disabilities and to applicants withsincerely heldreligious beliefs, practices, or observances. If you require assistance or accommodation during the application or interview process, please contact us atRecruitingUS@immatics.com.
Work Authorization
Applicants mustbe authorized towork in the United States without the need for current or future sponsorship.
Pre-Employment Requirements
Employment is contingent upon successful completion of a background check, referencechecksand pre-employment drug screening, wherepermittedby applicable law. For certain roles,additionalscreenings such as a credit check or motor vehicle record review may berequired, where job-related and consistent with business necessity.