Quality Inspector II | 2nd Shift (Monday-Friday)
About The Position
The Quality Inspector II assures the quality of products and batch records from manufacturing departments and evaluates quality issues with Manufacturing and Quality Assurance. The position works the 2nd shift, Monday through Friday, from 3:00 p.m. to 11:30 p.m., in Tampa, Florida. The listed starting pay is $20.00. The inspector conducts in-process inspections, reviews batch documentation, performs sampling and line-clearance activities, identifies potential nonconformances, and supports investigations and manufacturing operations. The role also helps ensure compliance with GMP, GxP, ISO, environmental health and safety procedures, and applicable standard operating procedures.
Requirements
- High school diploma required.
- At least 3 years of experience in a pharmaceutical or FDA-regulated facility, or a related field.
- Ability to work well with others and independently.
- Ability to follow written and verbal instructions and read and understand SOPs.
- Strong time-management skills and attention to detail.
- Maintain Quality Control, line-clearance, and visual-inspection certifications.
- Ability to work independently with little supervision.
- Ability to escalate or resolve shop-floor issues according to procedures using analytical and critical-thinking skills.
- Must be authorized to work for any employer in the United States; the employer is unable to sponsor or take over sponsorship of an employment visa.
Nice To Haves
- Associate degree preferred.
- Quality Control or Quality Assurance experience preferred.
Responsibilities
- Follow standard operating procedures and review batch records for Good Manufacturing Practices compliance, accuracy, completeness, and accountability.
- Monitor and conduct in-process inspections in manufacturing, applying documentation practices, visual inspections, testing intervals, and methods specified by batch records and current SOPs.
- Identify suspect material and perform segregation procedures when instructed by QA management or written instructions.
- Verify batch documents, including product, lot number, expiration dates, and components, and conduct on-line reviews.
- Perform AQL sampling and document inspection results in batch records.
- Perform LOTO, product inspections, line-clearance duties, and shift-change line verification according to procedures.
- Pull in-process samples and deliver them as required.
- Work with Materials Management, Contract Manufacturing, Engineering, and Validation; assist with and execute protocols and studies.
- Identify and notify appropriate departments of potential or observed nonconformances.
- Assist Manufacturing with issuing, correcting, and reviewing batch documents.
- Assist with batch-record review and closure at the end of each line run, including accountability and yield calculations.
- Complete required documentation reviews and work with Manufacturing to resolve outstanding issues before release to Quality Assurance.
- Evaluate quality issues and support investigations by providing necessary information and documentation.
- Support and participate in standardization and quality metrics.
- Support manufacturing schedules and changes.
- Maintain awareness of and compliance with GxP, ISO, and environmental health and safety procedures in the assigned area.
- Maintain compliance with GxP and procedural reading requirements and pursue personal development.
- Train other Quality Control employees.
- Perform other duties as assigned.
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
High school or GED
