Quality Inspector II; Third Shift

Quality Inspector II (Monday‑Friday Third Shift)

Shift: Monday – Friday / 11:00pm – 7:30am
Start Pay Range: $20.00

Objectives / Purpose of the Job: Assurance of quality product and batch records from the manufacturing departments, evaluating quality issues with Manufacturing and Quality Assurance.

• Follow standard operation procedures and review batch records to ensure compliance with Good Manufacturing Practices (GMP), accuracy, completeness, and accountability.
• Monitor and conduct in‑process inspections in the manufacturing area, implementing proper documentation practices, applicable visual inspections, testing intervals and/or methods as per batch record instructions and current SOP.
• Properly identify suspect material and perform segregation procedures, or when instructed by QA management and/or per provided written instructions.
• Check batch documents to ensure product, lot number, expiration dates and all components are correct, and conduct online reviews.
• Perform AQL sampling and document inspection results in the batch record.
• Perform LOTO, product inspections, and line clearance duties per procedures, and verify shift change line.
• Pull in‑process sampling and deliver accordingly.
• Interact with other departments including Materials Management, Contract Manufacturing, Engineering and Validation. Assist and execute protocols and studies.
• Identify and inform applicable departments in the event of a potential or observed nonconformance.
• Assist the manufacturing team with issuance, correction and review of batch documents.
• Assist Manufacturing team as needed with batch‑record reviews and batch‑record closure on each line at the end of the run, including accountability and yield calculations.
• Complete all required documentation review and work with the Manufacturing team to resolve outstanding issues before releasing to Quality Assurance.
• Evaluate quality issues and assist with investigations, providing necessary information and documentation when needed.
• Support and actively participate in standardization and Quality metrics.
• Support manufacturing schedules and changes.
• Assume responsibility for GxP, ISO, and environmental health and safety procedure awareness and compliance within the respective area.
• Maintain compliance to GxP and procedural reading, personal development.
• Perform training of other QCs.
• Any other duties as assigned.

• Associate’s degree preferred; high school diploma required.
• Quality Control/Assurance experience preferred.
• Ability to work well with people independently.
• Ability to follow written and verbal instructions and read and understand SOPs.
• Excellent time‑management skills and attention to detail.
• Maintain QC, line clearance and visual inspection certifications.
• Ability to escalated/solve shop‑floor issues per procedures using analytical and critical thinking skills.
• 3+ years of experience in a pharmaceutical/FDA‑regulated facility or related field required.

• No corrective actions at the written warning level in the last six months, no final warning level in the last 12 months, no active PIP.
• Meet the qualifications of the position as stated above.
• Be in current job for 12 months.
• Application position must be a step up in progression and not a step down.

Tampa, FL.

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.