Quality Inspector – In-Process Sampling

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Location:
Central Islip, NY (Onsite) – Full-Time, 1st Shift: 7:00 AM – 3:30 PM (may vary)

Reports To: QA Supervisor

Experience

Required:

1 – 13 Years (Minimum 1–2 years in pharma manufacturing/packaging)

Compensation: USD 33,000 – 46,000 per year ($16.64 – $22.88 per hour)

The QA Inspector I (1st Shift) monitors product quality throughout manufacturing phases, ensuring compliance with cGMP, SOPs, and established procedures. The role involves hands‑on inspections, sampling, SAP data entry, and shop floor oversight in generic pharmaceutical production.

• Verify raw materials during dispensing and post dispensed materials/samples into SAP system.
• Maintain standard weights and perform daily balance verifications.
• Conduct in‑process checks during batch manufacturing per batch record instructions. Collect in‑process samples (blend uniformity, finished product, validation samples) and perform basic testing (weight, thickness, hardness, disintegration, friability).
• Ensure equipment/area cleaning and provide line clearance.
• Review online batch records, area/equipment logbooks, calibration/PMP records, and engineering data (temperature/humidity).
• Perform daily shop floor quality rounds to maintain GMP compliance and elevate discrepancies to QA Manager.
• Isolate rejected materials, ensure accountability in batch records, and conduct AQL, blend sampling, in‑process inspections.
• Complete assigned training and follow company policies, safety, cGMP, and SOPs.

• 1–2 years experience in pharmaceutical manufacturing or packaging.
• Knowledge of Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP).
• Ability to read, write, and communicate effectively in a fast‑paced environment.
• Self‑motivated with strong multitasking, organizational skills, and attention to detail.
• Basic computer skills (Microsoft Word, PowerPoint, Excel; SAP experience preferred).

Minimum High School Diploma.

Entry level

Full-time

Quality Assurance

Software Development