Product Quality Inspector – Pharma

Mogi I/O : OTT/Podcast/Short Video Apps for you; Village of Westbury (NY); On-site; USD 33,000 - 46,000; Full time

Job summary

A pharmaceutical company in Central Islip, NY is seeking a QA Inspector I for a full-time role on the 1st shift. The ideal candidate will monitor product quality throughout manufacturing phases and ensure compliance with Good Manufacturing Practices (GMP) and established procedures. Responsibilities include inspecting raw materials, conducting in-process checks, and maintaining documentation. A minimum of 1-2 years of experience in pharma manufacturing or packaging and a High School Diploma are required. This is an on-site position offering a salary between $33,000 and $46,000 annually.

Qualifications

• 1–2 years experience in pharmaceutical manufacturing or packaging.
• Knowledge of Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP).
• Basic computer skills (Microsoft Word, PowerPoint, Excel; SAP experience preferred).

Responsibilities

• Verify raw materials during dispensing and post dispensed materials/samples into SAP system.
• Conduct in-process checks during batch manufacturing per batch record instructions.
• Perform daily shop floor quality rounds to maintain GMP compliance.

Skills

Knowledge of Good Manufacturing Practices (GMP)

Self-motivated with strong multitasking

Ability to read, write, and communicate effectively

Education

Minimum High School Diploma

Tools

SAP

Microsoft Word

Microsoft PowerPoint

Microsoft Excel

Job description

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)

Job Overview

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.

Key Responsibilities

• 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 escalate 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.

Must-Have Skills & Qualifications

• 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).

Education

Minimum High School Diploma.