Hiring.Camp

QA Technician – Weigh Room & Production Lines

NVE Pharmaceuticals

·

Apr 21, 2026

Salary
$18 – $24/hr
Location
Green Township, New Jersey
Type
Full-time
Department
IT
Experience
1+ years
Education
High School
Source
BetterTeam

Description

Position Summary:
The QA Technician – Weigh Room & Production Lines is responsible for in-process quality assurance activities during raw material dispensing, blending, encapsulation, and packaging operations. This role ensures compliance with cGMP requirements, internal procedures, and product specifications through real-time verification and documentation. Position is M-F 8am-4pm.

Key Responsibilities:
Weigh Room Oversight:
  • Verify raw materials against approved batch records prior to dispensing.
  • Confirm material status (released, quarantined, rejected).
  • Perform line clearance and room clearance checks before dispensing.
  • Verify accurate weighing of components (ID, item #, lot #, quantity).
  • Ensure calibrated scales are used and within calibration status.
  • Review and sign off on weigh room forms and other records.

Production Line QA (Blending / Encapsulation / Packaging):
  • Perform line clearance before start-up and between product changes.
  • Verify correct components, labels, and packaging materials are issued.
  • Conduct in-process checks (e.g., capsule weight variation, cosmetic checks, packaging checks).
  • Ensure equipment clean and ready to use.
  • Monitor adherence to GMP practices (personnel, documentation, sanitation).
  • Review batch documentation entries in real time for accuracy and completeness.

Documentation & Compliance:
  • Make all entries at the time of the work, ensure they are easy to read, and clearly show who recorded them.
  • Identify and escalate deviations, non-conformances, or out-of-spec conditions to management.
  • Support investigations as needed.
  • Maintain QA logbooks and inspection records.

Qualifications:
  • High school diploma required; Associate’s or Bachelor’s degree a plus.
  • 1–3 years experience in dietary supplement, food, or pharmaceutical manufacturing a plus but not required.
  • Familiarity with cGMP (21 CFR Part 111 preferred) a plus but not required.
  • Basic math and measurement skills required.
  • Strong attention to detail and documentation accuracy.

Key Competencies:
  • Detail-oriented with strong observational skills.
  • Ability to work on the production floor in a fast-paced environment.
  • Clear communication with production and QA teams.
  • Ability to enforce compliance standards consistently.

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

Skills

GMPCompliance

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