Quality Inspector II | 3rd Shift (Monday-Friday)

Bausch + Lomb (NYSE/TSX: BLCO) is a leading global eye health company dedicated to protecting and enhancing the gift of sight for millions of people around the world—from the moment of birth through every phase of life. Our mission is simple, yet powerful: helping you see better, to live better. Our comprehensive portfolio of over 400 products serves customers across the full spectrum of their eye health needs throughout their lives.

About the role

The role ensures the quality of product and batch records from the manufacturing departments and evaluates quality issues with Manufacturing and Quality Assurance.

Responsibilities

• Follows standard operating procedures and reviews batch records to ensure compliance with Good Manufacturing Practices (GMP), accuracy, completeness, and accountability.
• Monitors and conducts 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 identifies suspect material and performs segregation procedures, or follows instructions from QA management and/or provided written instructions.
• Checks batch documents to ensure product, lot number, expiration dates, and all components are correct, and conducts online reviews.
• Performs AQL sampling and documents inspection results in the batch record.
• Performs LOTO, product inspections, and line clearance duties per procedures.
• Performs shift change line verification.
• Pulls in-process sampling and delivers accordingly.
• Interacts with other departments including Materials Management, Contract Manufacturing, Engineering, and Validation.
• Assists and executes protocols and studies.
• Identifies and informs applicable departments in the event of a potential or observed nonconformance.
• Assists the manufacturing team with the issuance, correction, and review of batch documents.
• Assists with batch record reviews and batch record closure on each line at the end of the run, including accountability and yield calculations.
• Completes all required documentation review and works with the Manufacturing team to resolve outstanding issues before releasing to Quality Assurance.
• Evaluates quality issues and assists with investigations, providing necessary information and documentation when needed.
• Supports and actively participates in standardization and Quality metrics.
• Supports manufacturing schedules and changes.
• Assumes responsibility for GxP, ISO, and environmental health and safety procedure awareness and compliance within the respective area.
• Maintains compliance with GxP and procedural reading, and personal development.
• Performs training of other QCs.
• Performs any other duties as assigned.

Requirements

• Associates degree preferred; High School Diploma required.
• Quality Control/Assurance experience preferred (not required).
• 3+ years of experience in a pharmaceutical/FDA regulated facility or related field required.
• Ability to work well with people and independently.
• Ability to follow written and verbal instructions and read and understand SOPs.
• Excellent time management skills and attention to detail.
• Maintains QC, line clearance, and visual inspection certifications.
• Able to work independently with little supervision.
• Ability to escalate and solve shop floor issues per procedures, utilizing analytical and critical thinking skills.

Schedule

Monday–Friday, 11:00 PM – 7:30 AM

Pay

Start pay range: $20.00 per hour

Benefits

• Short-term and/or long-term incentives (U.S. based employees).
• Medical, dental, vision insurance.
• Disability and life insurance.
• 401(k) plan and company match.
• Tuition reimbursement program (select degrees).
• Company holidays.
• Well-being benefits.
• Sick time, floating holidays, and paid vacation.

Location: Tampa, FL