QA Inspector I

Job Title: QA Inspector I
Location: Central Islip, NY
Shift: 1st Shift (7:00 AM – 3:30 PM)
Job Type: Full-time, On-site
Pay Range: USD
Relocation: Local candidates preferred
Work Authorization: US Citizen or Green Card Holder only

Job Overview

A fast-growing pharmaceutical manufacturing facility in Central Islip is seeking a QA Inspector I. This role is responsible for monitoring and ensuring product quality throughout all phases of manufacturing in compliance with cGMP, SOPs, and internal quality standards. The ideal candidate will have experience in pharmaceutical manufacturing or packaging and be able to work in a fast paced environment with strong attention to detail.

Key Responsibilities

• Verify raw materials during the dispensing process.
• Post dispensed materials and samples into SAP and complete related transactions.
• Maintain standard weights and perform daily balance verifications.
• Conduct in-process checks during batch manufacturing as per batch record instructions.
• Collect in-process blend samples, finished product samples, validation samples, and perform blend uniformity sampling.
• Perform in-process testing such as weight, thickness, hardness, disintegration, and friability.
• Ensure proper cleaning of equipment and areas, and provide line clearance.
• Complete all assigned training and follow company policies, safety requirements, cGMP, and SOPs.
• Review online batch records, logbooks, calibration records, and preventive maintenance records.
• Ensure proper isolation of rejected materials and document accountability in batch records.
• Review engineering records such as temperature and humidity logs, calibration reports, and maintenance documentation.
• Conduct daily quality rounds to ensure shop floor compliance with GMP requirements.
• Escalate discrepancies or issues to Quality Assurance management.
• Perform AQL inspections, blend sampling, in-process sampling, and related quality checks.
• Support additional tasks assigned by management as needed.

Skills and Competencies

• Knowledge of Good Manufacturing Practices and Good Documentation Practices.
• Ability to read, write, and communicate clearly.
• Strong attention to detail, organization, and time management.
• Ability to work in a fast paced environment and handle multiple tasks.
• Basic computer proficiency, including Microsoft Word, PowerPoint, and Excel.

Education and Experience

• High school diploma required.
• Minimum 1–2 years of experience in pharmaceutical manufacturing or packaging.

Why Join

This role offers the opportunity to work in a reputable, growth-oriented pharmaceutical environment focused on quality, compliance, and operational excellence.

Pay: $16, $22,000.00 per year

Work Location: In person