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QA Validation Specialist

Job in Sanford, Lee County, North Carolina, 27330, USA
Listing for: SPECTRAFORCE
Full Time position
Listed on 2026-01-12
Job specializations:
  • Quality Assurance - QA/QC
    QA Specialist / Manager, Quality Control / Manager, Quality Engineering, Quality Technician/ Inspector
Salary/Wage Range or Industry Benchmark: 65 - 81 USD Hourly USD 65.00 81.00 HOUR
Job Description & How to Apply Below

Position Title

QA Validation Specialist

Work Location

Sanford, NC 27330

Assignment Duration

11 months

Work Schedule

8 AM - 4:30 PM

Work Arrangement

Onsite 4 days a week (5 days preferred; most team works 1 day remote)

Base Pay Range

$65.00/hr - $81.00/hr

Position Summary

The Specialist, QA Validation will be primarily responsible for the implementation, execution and assessment of quality systems, procedures, and records to support compliant GMP operations. This position works closely with Validation, Engineering, Manufacturing, Quality Control, Facilities, and Automation.

Key Responsibilities
  • Provide hands‑on QA support and oversight to internal staff and suppliers/contractors to ensure compliance with local and global quality standards, regulatory requirements, and industry guidance.
  • Provide QA review and approval for commissioning/qualification/validation documents.
  • Provide QA review and approval of qualification and validation deviations and discrepancies, and support investigation and corrective actions.
  • Author, review and approve controlled documents for the Quality organization including SOPs, specifications, protocols, and reports.
Qualification & Experience
  • B.S. degree in Biological/Physical/Chemical sciences, engineering, or equivalent focus of study and 3‑5+ years of experience OR M.S. degree and 1‑3+ years of experience in a QA function in a biologics manufacturing facility.
  • Experience with qualification/validation of process equipment, analytical instruments, clean utilities, automation, sterile filling, and clean facilities.
  • Strong understanding of FDA, EMA, local regulations and guidelines, ICH guidelines, and industry best practices.
  • Successful history working in a fast‑paced team environment, meeting deadlines, and prioritization of work from multiple projects.
  • Strong analytical and communication skills as well as sound judgment, with the ability to work effectively with others.
  • Excellent problem‑solving skills and experience with root cause investigations and CAPA determination.
  • Off hours coverage and flexibility may be required.
Seniority Level

Mid‑Senior level

Employment type

Contract

Job function

Quality Assurance

Industries

Pharmaceutical Manufacturing

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