Quality Assurance Inspector

Conduct visual inspections using measuring equipment such as calipers, crimp gauges, pressure gauges, and scales. MAJOR DUTIES AND RESPONSIBILITIES: Perform in-process and finished product inspections to ensure compliance with cGMP, SOPs, and regulatory requirements.

Quality Assurance Inspector

Title: Quality Assurance Inspector
Location: Largo, FL
Industry: Pharmaceutical Manufacturing
Schedule: 3rd Shift 11:00 PM 7:30 AM (possible rotating schedule)
Pay Rate: $24.00/hr + $3.00 shift differential ($27.00/hr)
Employment Type: Contract with the possibility to go permanent

MAJOR DUTIES AND RESPONSIBILITIES:

• Perform in-process and finished product inspections to ensure compliance with cGMP, SOPs, and regulatory requirements.
• Conduct visual inspections using measuring equipment such as calipers, crimp gauges, pressure gauges, and scales.
• Review and verify in-process quality checks throughout manufacturing.
• Verify pre-production and post-production line clearance activities.
• Perform daily verification and calibration checks of quality instruments, including scales and gauges.
• Monitor and verify temperature, pressure differential, equipment, and other quality logbooks.
• Review, record, and maintain quality documentation with a high level of accuracy.
• Collect and manage retain samples for Analytical and Microbiology Laboratories.
• Audit batch production records for accuracy, completeness, and compliance.
• Partner with Production to resolve quality-related issues and maintain product quality standards.
• Support the training of production personnel on quality procedures and inspection requirements.
• Provide quality support to Laboratory, Warehouse, Engineering, and Operations as needed.
• Participate in continuous improvement initiatives and other quality assurance projects.

QUALIFICATIONS:

• Associate's Degree preferred
• Manufacturing experience required.
• Previous experience in pharmaceutical, medical device, or other regulated manufacturing environments preferred.
• Knowledge of cGMP and Good Documentation Practices (GDP) preferred.
• Experience performing quality inspections in a manufacturing environment is a plus.
• Ability to work overtime or rotating schedules as needed.

CRITICAL SKILLS AND ABILITIES:

• Strong attention to detail and documentation accuracy.
• Ability to work independently in a fast-paced manufacturing environment.
• Strong organizational, problem-solving, and decision-making skills.
• Excellent verbal and written communication skills.
• Ability to maintain focus while performing detailed quality inspections.
• Team-oriented with a commitment to quality and continuous improvement.

COMPUTER SKILLS:

• Basic computer proficiency.
• Experience using Microsoft Office (Word and Excel).
• Ability to accurately complete quality documentation and production records.

PHYSICAL/ENVIRONMENTAL DEMANDS:

• Ability to stand and walk for extended periods.
• Frequent use of hands while performing inspections.
• Ability to lift up to 25 pounds.
• Exposure to manufacturing and pharmaceutical production environments.
• Exposure to chemicals and other potential workplace hazards while following established safety procedures.

EOE/ADA
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