QA Technician - Batch Reconciliation, AVP & Label Control

NVE Pharmaceuticals
Green, NJ

Position Summary:

The QA Technician – Batch Reconciliation, Approved Vendor Program, and Label Control is responsible for post-production quality review activities, including material reconciliation, supplier qualification support, and label verification to ensure compliance with regulatory and customer requirements. Position is M-F 8am-4pm

Key Responsibilities:

Batch Reconciliation:

  • Perform reconciliation of raw materials, bulk product, and finished goods.
  • Calculate yield percentages and identify discrepancies.
  • Investigate and flag variances outside established limits.
  • Ensure accountability of all materials used in production.
  • Support deviation investigations related to yield discrepancies.

Approved Vendor Program:

  • Maintain and update approved supplier list.
  • Review supplier documentation (COAs, questionnaires, certifications, scorecards).
  • Assist in supplier qualification and requalification processes.
  • Track expiration of vendor documents (GFSI certs, audits, insurance, etc.).
  • Coordinate with Purchasing and QA management on vendor approvals.

Label Proofing & Control:

  • Review and approve labels against customer specifications and approved artwork, contact Graphic Design department as needed for questions.
  • Verify accuracy of:
    • Supplement Facts panel.
    • Ingredient statements.
    • Allergen declarations.
    • Claims and formatting.
    • Cosmetic defects and overall visual appearance.

Documentation & Compliance:

  • Ensure reconciliation and label review records are complete and audit-ready.
  • Help Maintain traceability of materials and packaging components.
  • Identify and escalate discrepancies, mislabeling risks, or compliance gaps.
  • Support internal audits and regulatory inspections.

Qualifications:

  • High school diploma required; Associate’s or Bachelor’s degree preferred (Science related field).
  • >1 year QA experience in supplements, food, or pharma a plus but not required.
  • Strong understanding of cGMP and labeling requirements (21 CFR Part 111).
  • Experience with batch records and reconciliation calculations.
  • Proficient in Excel, Word, and Outlook.
  • Strong math ability.
  • HACCP or SQF (or other 3rd party quality or food safety certifications) a plus but not required.

Key Competencies:

  • Analytical mindset (especially with yield/reconciliation calculations).
  • Strong attention to detail (critical for label review).
  • Organizational skills for document and vendor tracking.
  • Ability to identify compliance risks proactively.


Benefits: We offer a comprehensive benefits package, including health insurance, paid time off, and retirement savings options.

Posted 2026-04-21

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