Quality Inspector II – GMP/QA, Evening Shift

Bausch + Lomb

Tampa (FL)

On-site

USD 23,000 - 32,000

Full time

2 days ago
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Job summary

Bausch + Lomb is seeking a Quality Control/Assurance professional in Tampa to ensure GMP-compliant batch records and product quality. You will monitor in-process inspections, identify nonconformances, and support cross-functional teams in documentation and compliance.

Ideal candidates have a relevant degree, QA experience, and strong attention to detail, with the ability to work independently and follow SOPs. This role aligns with our commitment to high-quality eye health products.

Qualifications

  • Associates degree preferred; high school diploma required.
  • Quality Control/Assurance experience preferred (not required).
  • Ability to work well with people and independently.
  • Be able to follow written and verbal instructions and read SOPs.
  • Excellent time management and attention to detail is critical.
  • Maintain QC, line clearance and visual inspection certifications.
  • 3+ years of pharmaceutical/FDA regulated facility or related field required.

Responsibilities

  • Follows standard operation procedures and reviews batch records to ensure GMP compliance.
  • Monitor in-process inspections and proper documentation practices.
  • Identify suspect material and perform segregation per instructions.
  • Check batch documents for product, lot numbers, expiration dates and components.
  • Performs AQL sampling and documents inspection results.
  • Interacts with Materials Management, Contract Manufacturing, Engineering and Validation.
  • Assist manufacturing with issuance, correction and review of batch documents.
  • Assist Manufacturing team with batch record closure and yield calculations.
  • Support GxP, ISO and health and safety compliance.

Skills

GMP compliance
QA procedures
In-process inspection
Batch record review

Education

Associates degree
High School Diploma

Job description

Bausch + Lomb is seeking a Quality Control/Assurance professional in Tampa to ensure GMP-compliant batch records and product quality. You will monitor in-process inspections, identify nonconformances, and support cross-functional teams in documentation and compliance.

Ideal candidates have a relevant degree, QA experience, and strong attention to detail, with the ability to work independently and follow SOPs. This role aligns with our commitment to high-quality eye health products.

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