Quality Inspector – In-Process Sampling

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

Job summary

A pharmaceutical manufacturing company in Central Islip, NY is seeking a QA Inspector I for the first shift. The role involves monitoring product quality and ensuring compliance with GMP regulations. Ideal candidates will have 1-2 years of experience in pharma manufacturing or packaging, strong attention to detail, and basic computer skills. This is a full-time, onsite position offering competitive compensation. Join a team dedicated to maintaining the highest quality in production.

Qualifications

• 1–2 years experience in pharmaceutical manufacturing or packaging.
• Ability to read, write, and communicate effectively in a fast‑paced environment.
• Self‑motivated with strong multitasking and organizational skills.

Responsibilities

• Monitor product quality throughout manufacturing phases.
• Verify raw materials and conduct in‑process checks.
• Perform daily shop floor quality rounds to maintain GMP compliance.

Skills

Knowledge of Good Manufacturing Practices (GMP)

Attention to detail

Multitasking

Basic computer skills (Microsoft Word, Excel)

Education

High School Diploma

Tools

SAP

Job description

1 day ago Be among the first 25 applicants

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 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.

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.

Seniority Level

Entry level

Employment Type

Full-time

Job Function

Quality Assurance

Industries

Software Development