Quality Assurance InspectorTitle: Quality Assurance Inspector
Location: Largo, FL
Industry: Pharmaceutical Manufacturing
Schedule: 11pm-7:30am
Pay Rate: $22+$3 shift differential = $25/hr
Employment Type: Contract with the possibility to go permanent
MAJOR DUTIES AND RESPONSIBILITIES:- Adhere to all company policies, procedures, and Standard Operating Procedures (SOPs).
- Demonstrate and maintain compliance with Good Documentation Practices (GDP) and current Good Manufacturing Practices (cGMP).
- Perform finished product inspections using measuring equipment including calipers, crimp gauges, pressure gauges, scales, and visual inspection techniques.
- 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 instrumentation, including scales and gauges.
- Monitor and verify monthly logbooks, including temperature, pressure differential, equipment, and related records.
- Accurately review, record, and maintain quality documentation.
- Collect and manage retain samples and samples for Analytical and Microbiology Laboratories.
- Audit batch production records to ensure accuracy, completeness, and compliance.
- Serve as a liaison between the Quality and Production departments to resolve quality-related issues.
- Assist with the training and development of IPQA Inspector I team members.
- Train and support Line Leaders and Production Assemblers on in-process inspection requirements and quality procedures.
- Demonstrate proficiency performing quality inspections across all production machine lines.
- Provide quality support to other departments, including Laboratory, Warehouse, Engineering, and Operations, as needed.
- Promote continuous improvement initiatives and support customer satisfaction objectives.
- Participate in additional quality assurance activities and special projects as assigned by Quality Management.
QUALIFICATIONS:- High School Diploma or equivalent required.
- Working knowledge of FDA regulations applicable to pharmaceutical and/or medical device manufacturing.
- Knowledge of quality inspection requirements for aerosol, tube, and liquid products.
- Previous experience performing quality inspections in a regulated manufacturing environment preferred.
- Proficient in the use of personal computers and quality measuring instruments.
- Strong attention to detail with excellent documentation accuracy.
- Ability to prioritize work, manage multiple responsibilities, and work independently with minimal supervision.
- Capable of performing effectively in a fast-paced manufacturing environment with changing priorities.
- Strong problem-solving and decision-making skills.
- Excellent verbal and written communication skills.
- Ability to maintain concentration while performing detailed quality inspections.
- Demonstrated initiative, technical aptitude, and commitment to achieving departmental and company objectives.
- Ability to work collaboratively with cross-functional teams while promoting a culture of quality and continuous improvement.
PHYSICAL/ENVIRONMENTAL DEMANDS:- Ability to stand and walk frequently throughout the shift.
- Ability to sit occasionally as needed.
- Frequent lifting of up to 10 pounds and occasional lifting of up to 25 pounds.
- Continuous use of hands for handling, touching, and performing detailed inspection tasks.
- Occasional reaching above shoulders, stooping, kneeling, crouching, or crawling.
- Ability to communicate verbally and hear continuously throughout the workday.
- Potential exposure to chemicals and other workplace hazards.
- Work may involve exposure to varying environmental conditions, including heat, cold, or humidity.
EOE/ADA
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