Quality Inspector II

About the role

Bausch + Lomb (NYSE/TSX: BLCO) is a leading global eye health company dedicated to protecting and enhancing the gift of sight. This role ensures product compliance through the inspection of incoming material and the release of final product.

Key Activities/Responsibilities

• Inspect and measure incoming materials and components using calibrated measuring instruments to make a timely disposition on all incoming raw materials to ensure inspection and test results are in accordance with QA procedures.
• Review final product quality records and verify counts for evidence of compliance with the quality system transactions to release outgoing products via BLUR/paper quality records.
• Notify chemistry for receipts that require lab analysis.
• Review sterilization records/documentation and approve the release of autoclave cycles.
• Disposition incoming products and label containers to reflect the inspection and test results in accordance with procedures.
• Place and remove lots on hold through interaction with purchasing, manufacturing, and quality. Perform database (PeopleSoft) system transactions to release accepted incoming material and components.
• Document inspection results and maintain filing systems.
• Interpret procedures and specifications to accurately disposition product.
• Ensure nonconforming and in-process material is properly identified, labeled and segregated for compliance to established quality standards.
• Maintain records in accordance with the Record Retention Policies.
• Other duties as assigned.

Qualifications/Training

• High school diploma or equivalent, required.
• Must be able to interpret blueprints, component drawings and color standards.
• Must be able to read, write and speak English.
• Must possess basic math, interpersonal and organizational skills.
• Working knowledge of Excel, Word, and various testing instruments is necessary.
• Ability to prioritize workload and attention to detail is required.
• Must have schedule flexibility including possible overtime.
• Must meet physical requirements (medical clearance is required).
• Experience: 3+ years of experience in a GMP environment preferred.

Benefits

This position may be available in the following location(s): US - Rochester, NY (Plant)

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.

For U.S. locations that require disclosure of compensation, the starting pay for this role is between $18.00 - $24.00 per hour. The estimated salary range reflects an anticipated range for this position. The actual base salary offered may depend on a variety of factors.

U.S. based employees may be eligible for short-term and/or long-term incentives. They may also be eligible to participate in medical, dental, vision insurance, disability and life insurance, a 401(k) plan and company match, a tuition reimbursement program (select degrees), company holidays, and well-being benefits, among others. U.S. based employees are also eligible to receive sick time, floating holidays and paid vacation.