More jobs:
QA Validation Specialist
Job in
Sanford, Lee County, North Carolina, 27330, USA
Listed on 2026-01-12
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
Job Description & How to Apply Below
Position Title
QA Validation Specialist
Work LocationSanford, NC 27330
Assignment Duration11 months
Work Schedule8 AM - 4:30 PM
Work ArrangementOnsite 4 days a week (5 days preferred; most team works 1 day remote)
Base Pay Range$65.00/hr - $81.00/hr
Position SummaryThe 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.
- 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.
Mid‑Senior level
Employment typeContract
Job functionQuality Assurance
IndustriesPharmaceutical Manufacturing
#J-18808-LjbffrTo View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
Search for further Jobs Here:
×