
QA Computer Systems Validation (CSV) Specialist
Wilson, NCJob$60/hrSeen todaySeen in employer's feed today
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At a glance
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Requirements
Credentials this posting asks for.
Job overview
The QA Validation Specialist will join the Quality Assurance department to support validation and compliance initiatives in a pharmaceutical environment. The role focuses on validation activities for equipment, utilities, and manufacturing processes, maintaining validated systems, and supporting audits. The specialist will collaborate with Engineering and Validation teams to help ensure equipment and processes meet GMP and validation requirements.
Skills & qualifications
Skills
Qualifications
Benefits
Full job description
Our client, a leading organization in the pharmaceutical industry, is seeking a dedicated QA Validation Specialist to join their team. As a QA Validation Specialist, you will be part of the Quality Assurance department supporting validation and compliance initiatives. The ideal candidate will demonstrate attention to detail, proactive problem-solving skills, and excellent communication abilities, which will align successfully within the organization.
Job Title: QA Validation Specialist
Location: Wilson, North Carolina
Pay Range: $60
What's the Job?
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Define and establish scope, objectives, and strategic approach for validation activities to ensure regulatory and quality standards are met.
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Support the development and review of validation protocols (IQ/OQ/PQ) for equipment, utilities, and manufacturing processes.
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Maintain validated systems through periodic reviews, requalification, and change control assessments.
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Collaborate with Engineering and Validation teams to ensure equipment design, installation, and operation meet GMP and validation requirements.
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Support internal and external audits by providing validation documentation and subject matter expertise.
What's Needed?
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Bachelor’s degree in Life Sciences, Engineering, or a related field.
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3+ years of validation experience in a pharmaceutical environment.
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Knowledge of regulatory guidelines (FDA, EMA, ICH Q7–Q10), GAMP 5, and data integrity principles.
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Proficiency in Microsoft Office Suite and validation software tools.
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Strong analytical, documentation, and communication skills.
What's in it for me?
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Opportunity to work in a dynamic and compliant pharmaceutical environment.
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Engage in meaningful validation projects that impact product quality and patient safety.
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Collaborate with cross-functional teams to drive continuous improvement.
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Develop your professional skills through challenging validation activities.
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Be part of a company committed to quality, compliance, and employee growth.
Upon completion of waiting period consultants are eligible for:
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Medical and Prescription Drug Plans
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Dental Plan
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Vision Plan
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Health Savings Account
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Health Flexible Spending Account
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Dependent Care Flexible Spending Account
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Supplemental Life Insurance
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Short Term and Long Term Disability Insurance
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Business Travel Insurance
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401(k), Plus Match
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Weekly Pay
If this is a role that interests you and you'd like to learn more, click apply now and a recruiter will be in touch with you to discuss this great opportunity. We look forward to speaking with you!
About ManpowerGroup, Parent Company of: Manpower, Experis and Talent Solutions.
Experis® is a global leader in technology services and part of the ManpowerGroup® (NYSE: MAN) family of brands. We connect skilled technology professionals with meaningful opportunities where they can grow their careers, expand their expertise and make a real impact. Guided by the belief that it takes Human Ingenuity to unlock the true potential of technology, Experis helps people gain experience with leading organizations, build sought-after skills and take the next step toward a brighter future. Backed by ManpowerGroup's 75+ years of workforce expertise and global reach across more than 70 countries and territories, Experis brings the scale, insight and opportunity to help people and businesses thrive. ManpowerGroup is consistently recognized for its commitment to inclusion, ethics and responsible business, including being named one of the World's Most Ethical Companies. Learn more at Experis.com.
ManpowerGroup is committed to providing equal employment opportunities in a professional, high quality work environment. It is the policy of ManpowerGroup and all of its subsidiaries to recruit, train, promote, transfer, pay and take all employment actions without regard to an employee's race, color, national origin, ancestry, sex, sexual orientation, gender identity, genetic information, religion, age, disability, protected veteran status, or any other basis protected by applicable law.
How this job compares
Set against the 4,809 open Quality Assurance jobs on Olive Jobs, counted November 11, 2026.
- Pay
- This posting$60/hr
- North Carolina median$30–39/hr26 hourly ranges
- US median$26–31/hr807 hourly ranges
This rate, $60/hr, is 61% above the North Carolina median midpoint ($37/hr) — in the top quarter of Quality Assurance hourly ranges in North Carolina.
- Openings
- Olive Jobs lists 222 open Quality Assurance jobs in North Carolina and 4,809 across the US. 3% of them nationwide are listed as remote or flexible.
- Hiring the most in North Carolina
- Fujifilm9 open
- STG International9 open
- Actalent8 open
- Experience
- This posting asks for at least 3 years of experience; Quality Assurance postings that state a minimum ask for 5 years at the median (3,704 postings).
- Education
- This posting asks for a bachelor's degree; 1,659 of the 4,809 open Quality Assurance jobs (34%) ask for a bachelor's degree or higher.
Counted across the open, public US postings on Olive Jobs on November 11, 2026. Pay medians are the middle values of the low ends and of the high ends of postings that list both ends of a range in the same cadence (a yearly salary or an hourly rate); a range's midpoint is halfway between its ends. Pay and experience figures resting on fewer than 20 postings are left out.
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