Impactful QA Validation Specialist – Pharma Compliance

Experis Technology Group; Wilson (NC); On-site; USD 68,000 - 97,000; Full time

Benefits offered by this job

Medical and Prescription Drug Plans

Dental Plan

Vision Plan

Health Savings Account

Health Flexible Spending Account

Dependent Care FSA

Supplemental Life Insurance

Short Term Disability Insurance

Long Term Disability Insurance

Business Travel Insurance

401(k) with Match

Weekly Pay

Job summary

Experis Technology Group is seeking a QA Validation Specialist in Wilson, NC to support validation initiatives within the Quality Assurance department. You will help define scope, develop IQ/OQ/PQ protocols, and maintain validated systems to ensure regulatory and quality standards are met.

The ideal candidate has a Bachelor’s degree in Life Sciences or Engineering, 3+ years of pharma validation experience, and strong communication skills.

Qualifications

• Bachelor’s degree in Life Sciences, Engineering, or a related field.
• 3+ years of validation experience in a pharmaceutical environment.
• Knowledge of FDA, EMA, ICH Q7–Q10, GAMP 5, and data integrity.
• Proficiency in Microsoft Office Suite and validation software tools.
• Strong analytical, documentation, and communication skills.

Responsibilities

• Define scope and approach for validation activities to meet regulatory standards.
• Develop and review IQ/OQ/PQ protocols for equipment, utilities, and processes.
• Maintain validated systems via reviews, requalification, and change control.
• Collaborate with Engineering and Validation teams to ensure GMP compliance.
• Support audits by providing validation documentation and SME input.

Skills

Attention to detail

Proactive problem-solving

Excellent communication

Education

Bachelor’s degree in Life Sciences/Engineering

Tools

Microsoft Office

Validation software

Job description

Experis Technology Group is seeking a QA Validation Specialist in Wilson, NC to support validation initiatives within the Quality Assurance department. You will help define scope, develop IQ/OQ/PQ protocols, and maintain validated systems to ensure regulatory and quality standards are met.

The ideal candidate has a Bachelor’s degree in Life Sciences or Engineering, 3+ years of pharma validation experience, and strong communication skills.