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Quality Assurance Validation Associate Jobs (NOW HIRING)

LeadStack Inc.

GMP QA Validation Specialist

Durham, NC · On-site

$45 - $53/hr

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 Associate Director, GMP Quality Assurance ...

System One

QA Validation Engineer

Bethlehem, PA · On-site

Job Title: QA Validation Engineer Location: Bethlehem, PA Type: Direct Hire Compensation: $95-110k Work Model: Onsite - onsite Hours: M-F 8:30A - 5P Responsibilities * Arranges, plans, manages and ...

System One

QA Validation Engineer

Bethlehem, PA · On-site

Job Title: QA Validation Engineer Location: Bethlehem, PA Type: Direct Hire Compensation: $95-110k Work Model: Onsite - onsite Hours: M-F 8:30A - 5P Responsibilities * Arranges, plans, manages and ...

Initial Therapeutics, Inc.

NY · On-site

$78K - $107K/yr

We are seeking a Sr. QA Validation Specialist to join our Quality Assurance team. As the Senior QA Validation Specialist, you will validate/qualify equipment, systems, and processes in accordance ...

System One

QA Validation Engineer

Bethlehem, PA · On-site

Job Title: QA Validation Engineer Location: Bethlehem, PA Type: Direct Hire Compensation: $95-110k Work Model: Onsite - onsite Hours: M-F 8:30A - 5P Responsibilities * Arranges, plans, manages and ...

LeadStack Inc.

GMP QA Validation Specialist

Durham, NC · On-site

$45 - $53/hr

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 Associate Director, GMP Quality Assurance ...

Scorpion Therapeutics

NY · On-site

$78K - $107K/yr

S. in life sciences or related field; proven experience may substitute. * QA Validation Specialist: 4+ years of experience. * Sr. QA Validation Specialist: 6+ years of experience. Benefits (if part ...

Regeneron Pharmaceuticals, Inc

NY · On-site

$78K - $107K/yr

We are seeking a Sr. QA Validation Specialist to join our Quality Assurance team. As the Senior QA Validation Specialist, you will validate/qualify equipment, systems, and processes in accordance ...

Danaher

Manager Quality Assurance, Validation

Chaska, MN · On-site

$130K - $160K/yr

This position will manage professional associates and operation support assigned to the Quality Assurance line support and validation team management, equipment program management, Design Change ...

Danaher

Manager Quality Assurance, Validation

Chaska, MN · On-site

$130K - $160K/yr

This position will manage professional associates and operation support assigned to the Quality Assurance line support and validation team management, equipment program management, Design Change ...

Kellton Tech

QA Validation Technician I

Tampa, FL · On-site

... quality assurance in a cGMP-regulated environment. This individual will contribute to method development, validation, troubleshooting, and support project timelines while ensuring data integrity and ...

Scorpion Therapeutics

NY · On-site

$78K - $107K/yr

Requires B.S. in life sciences or related field; may substitute proven experience for education * QA Validation Specialist: 4+ years of experience * Sr. QA Validation Specialist: 6+ years of ...

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How much do quality assurance validation associate jobs pay per hour?

As of Sep 13, 2026, the average hourly pay for quality assurance validation associate in the United States is $29.29, according to ZipRecruiter salary data. Most workers in this role earn between $18.75 and $34.38 per hour, depending on experience, location, and employer.

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Infographic showing various Quality Assurance Validation Associate job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 13% Part Time, 4% Contract, and 1% Nights. Highlights an 84% Physical, 1% Hybrid, and 15% Remote job distribution, with an average salary of $60,925 per year, or $29.3 per hour.

GMP QA Validation Specialist

Durham, NC • On-site

LeadStack Inc.
Recruiting and Staffing Services • 51 - 200 employees
Learn more about LeadStack Inc.external

$45 - $53/hr

Full-time

This job post has expired today. Applications are no longer accepted.

Job description

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 Associate Director, GMP Quality Assurance, will be responsible for ensuring the compliant onboarding, qualification, and validation of equipment, instruments, and computerized systems against corporate procedures, and applicable GMP national, international, and state regulations. Acting as a key QA partner to technical and operational teams, this role will provide expert oversight and quality support throughout the lifecycle of validation activities, from planning and development through execution and final approval. This role will assist in the management of Quality Management System (QMS) and will strongly support Culture of Quality. The position will be based at our headquarters facility in RTP, NC with no travel expected.

Job Responsibilities

  • Work alongside department customers on development, implementation, and integration of Equipment and Computer Systems Validation plans for site wide equipment onboarding.
  • Provide timely quality support and thorough reviews and approvals of various records including, but not limited to; equipment and computer system qualification and validation documents, SOPs, Change Controls, non-conformities, Deviations and Corrective Action/Preventive Action (CAPAs).
  • Ensure QA related activities are performed within the associated project timeline. Effectively escalate concerns to area and project management.
  • Report on applicable key metrics to drive continuous improvement in compliance.
  • Participate in project meetings as a quality lead and support colleagues by acting as a technical resource for quality and compliance related issues. Effectively collaborate in team environment(s) to ensure timely resolution of compliance and process concerns associated with equipment/computer systems validation activities.
  • Maintain Quality Systems in support of QMS and GMPs, including:
    • Support equipment and computer system qualification and validation activities and vendor management program.
    • Review and approve SOP drafts and revisions.
    • Support, review and approve assigned change control records.
  • Communicate project status to stakeholders and escalate issues in a timely manner.
  • Support ongoing Computerized Maintenance Management System records, including review and approval of work order records.

About You

Bachelor's degree in a scientific field.

5+ years of experience in pharmaceutical, biotech, or biologics GMP regulated manufacturing environment with 3+ years in Quality and/or Manufacturing.

Solid understanding of GMP guidelines and Quality Systems with the ability to apply GMPs in conformance to U.S. standards, and where appropriate, other regulatory authority standards.

Strong technical understanding of equipment and system validation principles.

Ability to author, review, and interpret Standard Operating Procedures (SOPs).

Ability to identify and/or resolve quality issues/discrepancies with others in a proactive, diplomatic, flexible, and constructive manner.

Strong attention to detail, highly organized and the ability to multitask in a fast-paced, highly interactive environment.

Ability to manage workload effectively in order to meet project timelines.

Excellent verbal and written communication skills, and the ability to effectively collaborate with peers including scientific/technical colleagues across a dynamic GMP environment.

Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).

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