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

Bausch + Lomb•US-FL-Tampa, FL

13h•Onsite

About The Position

The assurance of quality product and batch records from the manufacturing departments. Evaluates quality issues with Manufacturing and Quality Assurance.

Requirements

High School Diploma Required.
Quality Control/Assurance experience preferred (not 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.
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.

Nice To Haves

Associates degree preferred.

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.