Job Description

Job Title: QA Inspector

Location: Hauppauge & Central Islip, NY

Job Type: Full-Time

Department: Quality Assurance

About the Company

We are a leading generic pharmaceutical manufacturing company with state-of-the-art facilities in Hauppauge and Central Islip, NY. We are committed to producing high-quality medicines that meet regulatory standards and improve patient lives. We are currently expanding our teams across multiple departments, including Warehouse, Packaging, Manufacturing, QA Document Control, and more .

Position Summary

The QA Inspector is responsible for ensuring that products, processes, and documentation comply with current Good Manufacturing Practices (cGMP), company policies, and regulatory requirements. This role involves in-process checks, batch record review, and oversight of production activities to maintain the highest level of quality and compliance.

Key Responsibilities

• Perform in-process inspections in manufacturing, packaging, and warehouse areas to ensure compliance with cGMP.
• Review batch records, logbooks, and supporting documentation for accuracy and completeness.
• Verify line clearance, equipment cleanliness, and readiness prior to manufacturing and packaging operations.
• Conduct sampling of raw materials, in-process materials, and finished products as per SOPs.
• Monitor adherence to Standard Operating Procedures (SOPs), regulatory requirements, and internal quality policies.
• Document deviations, non-conformances, and report findings to QA management.
• Support investigations, CAPAs, and change controls as required.
• Ensure compliance with safety, sanitation, and quality standards throughout the facility.
• Provide guidance to production teams to maintain compliance during daily operations.
• Collaborate with cross-functional departments to resolve quality-related issues.

Qualifications

• Bachelor’s degree in Pharmaceutical Sciences, Chemistry, Biology, or related discipline preferred.
• Minimum of 1–3 years QA experience in pharmaceutical manufacturing (OSD, sterile, or packaging).
• Strong knowledge of cGMP, FDA, and regulatory guidelines .
• Experience with documentation review and in-process quality inspections.
• Excellent attention to detail, organizational, and communication skills.
• Ability to work independently and collaboratively in a fast-paced environment.

Skills & Competencies

• Knowledge of pharmaceutical production processes (Manufacturing, Packaging, Warehouse).
• Strong documentation and record-keeping abilities.
• Problem-solving and decision-making skills.
• Familiarity with QA Document Control processes.
• Ability to multitask and manage priorities.

What We Offer

• Competitive base salary
• Comprehensive benefits package (Medical, Dental, Vision, 401(k) with match)
• Paid Time Off (PTO), Holidays, and Sick Leave
• Professional growth opportunities in a fast-growing pharmaceutical company

Equal Opportunity Employer: We value diversity and are committed to creating an inclusive environment for all employees.

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