QA Technician - Weigh Room & Production Lines

NVE Pharmaceuticals; Andover (NJ); Presencial; USD 42 000 - 62 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Health insurance

Paid time off

Retirement savings options

Resumo da oferta

NVE Pharmaceuticals seeks a QA Technician – Weigh Room & Production Lines to oversee in-process QA during dispensing, blending, encapsulation, and packaging. You will verify materials against batch records, ensure proper labeling, and document findings in real time to support cGMP compliance.

The role covers weigh room oversight, production line QA, and documentation/compliance, with a Monday–Friday 8am–4pm schedule. Strong attention to detail and basic math skills are essential.

Qualificações

• 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.

Responsabilidades

• 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.
• 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.

Conhecimentos

Basic math

Measurement skills

Documentation accuracy

Attention to detail

Clear communication

Formação académica

High school diploma

Associate/Bachelor’s degree

Descrição da oferta de emprego

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.

Job Description

Job 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 elevate 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

• health insurance
• paid time off
• retirement savings options