Quality Inspector II (Monday-Friday Third Shift)

Date: Jun 2, 2026 Location: US-FL-Tampa, US Shift: Monday – Friday / 11:00pm – 7:30am Start Pay Range: $20.00 Objectives / Purpose of the Job The assurance of quality product and batch records from the manufacturing departments. Evaluates quality issues with Manufacturing and Quality Assurance. Key Activities / Responsibilities / Job Functions 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. Perform shift change line verification. 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 the 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. Qualifications / Training Associate’s degree preferred; high school diploma required. Quality Control/Assurance experience preferred (not required). 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 are critical. Maintain QC, line clearance and visual inspection certifications. Able to work independently with little supervision. Ability to elevate/solve shop‑floor issues per procedures and utilize analytical and critical thinking skills. 3+ years of pharmaceutical/FDA‑regulated facility or related field experience required. Eligibility for Internal Applicants Have no corrective actions at the written warning level in the last six months, no final warning level in the last 12 months, and no active PIP. Meet the qualifications of the position as stated above. Be in current job for 12 months. Position applying for must be a step up in progression and not a step down. 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. Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time. To learn more about job offer fraud, please read Bausch+Lomb's Job Offer Fraud Statement. Benefits are provided. For detailed information visit Bausch + Lomb benefits page. #J-18808-Ljbffr