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

Worklane GmbH; Tampa (FL); On-site; USD 28,000 - 34,000; Full time

Benefits offered by this job

Health insurance

401(k) plan

Tuition reimbursement

Paid time off

Job summary

Bausch + Lomb is seeking a QA/QC professional to assure quality products and batch records from manufacturing. The role involves GMP-compliant inspections, document reviews, and collaboration with Materials Management, Contract Manufacturing, Engineering and Validation.

Qualification requirements include an Associates degree preferred or a high school diploma, with 3+ years in pharma/FDA environments. The position is located in Tampa, FL and offers standard U.S. benefits.

Qualifications

• 3+ years of pharmaceutical/FDA regulated facility or related field required.
• Quality Control/Assurance experience preferred (not required).
• Ability to follow written and verbal instructions and read SOPs.

Responsibilities

• Follow SOPs and review batch records for GMP compliance.
• Conduct in-process inspections and document results.
• Identify and segregate suspect material per QA directions.
• Verify batch documents: product, lot number, expiration dates.

Skills

Time management

Reading SOPs

Attention to detail

Independence

Education

Associates degree preferred

High School Diploma required

Job description

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 is fully integrated and built to serve our customers across the full spectrum of their eye health needs throughout their lives. Our iconic brand is built on the deep trust and loyalty of our customers established over our 170-year history. We have a significant global research, development, manufacturing and commercial footprint of approximately 13,000 employees and a presence in approximately 100 countries, extending our reach to billions of potential customers across the globe. We have long been associated with many of the most significant advances in eye health, and we believe we are well positioned to continue leading the advancement of eye health in the future.

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:

• 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.

Qualifications /Training:

• Associates degree preferred. 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.

This position may be available in the following location: US - Tampa, FL

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.

• 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.

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.