Quality Assurance Inspector

We are seeking a detail-oriented Quality Assurance Inspector to support quality assurance activities within a pharmaceutical manufacturing environment. This role is responsible for ensuring compliance with current Good Manufacturing Practices (cGMP), company policies, and regulatory requirements while supporting manufacturing operations and maintaining product quality.

Shift: 2:00 PM - 10:30 PM (M -F)

Key Responsibilities

• Monitor compliance with cGMP guidelines, SOPs, and quality standards.
• Perform routine GMP audits and manufacturing floor walkthroughs.
• Conduct visual inspections and cleaning verification of manufacturing equipment and production areas.
• Review completed manufacturing documentation for accuracy and compliance.
• Perform Acceptance Quality Limit (AQL) inspections as required.
• Place materials and products on quality hold when necessary.
• Support investigations, quality documentation, and continuous improvement initiatives.
• Collaborate with Manufacturing, Quality Control, and other cross-functional teams to maintain regulatory compliance.
• Perform additional quality-related responsibilities as assigned.

Required Qualifications

• High school diploma or equivalent required; additional education in a science or technical field is a plus.
• Minimum of 2 years of experience in pharmaceutical manufacturing, quality assurance, or a regulated manufacturing environment.
• Strong understanding of current Good Manufacturing Practices (cGMP).
• Experience supporting manufacturing operations in a pharmaceutical environment.
• Knowledge of manufacturing processes such as granulation, blending, coating, printing, and equipment cleaning verification is preferred.
• Ability to work independently with minimal supervision while demonstrating sound decision-making skills.
• Strong attention to detail and documentation accuracy.
• Effective verbal and written communication skills.
• Basic computer proficiency and experience using electronic documentation systems.

Preferred Skills

• Experience performing GMP audits and manufacturing walkthroughs.
• Familiarity with batch record review and quality documentation.
• Strong analytical, organizational, and problem-solving abilities.
• Ability to work effectively in a fast-paced, team-oriented manufacturing environment.

Work Environment

• Manufacturing and production environment requiring adherence to safety procedures and quality standards.
• May require the use of personal protective equipment (PPE).
• Position involves standing, walking, visual inspections, and occasional lifting of up to 25 lbs.