Quality Assurance Inspector
$24 per hourThe Staffing Resource Group Inc
Job Description 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:
IND123
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.
- Associate's Degree required.
- 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.
- 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.
- Basic computer proficiency.
- Experience using Microsoft Office (Word and Excel).
- Ability to accurately complete quality documentation and production records.
- 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.
IND123
Vacancy posted 1 day ago
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