Quality Inspector II (Monday-Friday:Second Shift) jobs in United States
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Bausch + Lomb France · 1 day ago

Quality Inspector II (Monday-Friday:Second Shift)

Bausch + Lomb is a leading global eye health company dedicated to protecting and enhancing the gift of sight for millions of people. The Quality Inspector II will ensure the quality of products and batch records from the manufacturing departments, monitor inspections, and assist with documentation and compliance with Good Manufacturing Practices (GMP).

Medical Device
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Responsibilities

Follows standard operation procedures and review to 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 identifies suspect material and performs 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 conducts on line 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
Pull in-process sampling and deliver accordingly
Interacts with other departments including Materials Management, Contract Manufacturing, Engineering and Validation. Assists and executes 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
Completes all required documentation review and work with the Manufacturing team to resolve outstanding issues before releasing to Quality Assurance
Evaluates quality issues and assists with the investigations providing necessary information and documentation when needed
Supports and actively participates in standardization and Quality metrics
Support of manufacturing schedules and changes
Assume the responsibility for the 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

Qualification

Quality ControlManufacturing PracticesPharmaceutical experienceAnalytical skillsAttention to detailTime managementTeamworkProblem-solvingCommunication skills

Required

High School Diploma Required
Ability to work well with people an independently
Be able to follow written and verbal instructions and ability to read and understand SOP's
Excellent time management skills and attention to detail is critical
Maintain QC, line clearance and visual inspection certifications. Able to work independently with little supervision
Ability to escalate/solve shop floor issues per procedures and utilizing analytical and critical thinking skills
3+ years of pharmaceutical/FDA regulated facility or related field required

Preferred

Associates degree preferred
Quality Control/Assurance experience preferred (not required)

Company

Bausch + Lomb France

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Bausch+Lomb, c’est avant tout un laboratoire dédié à la protection et à l’amélioration de la vue de millions de personnes dans le monde, pour les accompagner dès leur naissance et à chaque phase de leur vie.

Funding

Current Stage
Growth Stage
Company data provided by crunchbase