Quality Inspector II | 2nd Shift (Monday-Friday)
About The Position
The Quality Inspector II assures the quality of products and batch records from manufacturing departments and evaluates quality issues in collaboration with Manufacturing and Quality Assurance. The role monitors and conducts in-process inspections, checks batch documentation, samples and inspects products, and supports line clearance and manufacturing quality activities. The position also assists with investigations, documentation resolution, batch record closure, and training other Quality Control employees. The role is based in Tampa, Florida, and is scheduled Monday through Friday from 3:00 p.m. to 11:30 p.m. The listed starting pay is $20.00.
Requirements
- High school diploma required.
- At least 3 years of experience in a pharmaceutical/FDA-regulated facility or a related field required.
- Ability to work well with people and independently.
- Ability to follow written and verbal instructions and read and understand SOPs.
- Excellent time-management skills and attention to detail.
- Maintain QC, line-clearance, and visual-inspection certifications.
- Ability to work independently with little supervision.
- Ability to escalate or solve shop-floor issues according to procedures using analytical and critical-thinking skills.
Nice To Haves
- Associate degree preferred.
- Quality Control or Quality Assurance experience preferred.
Responsibilities
- Follow standard operating procedures and review batch records for Good Manufacturing Practices (GMP) compliance, accuracy, completeness, and accountability.
- Monitor and conduct in-process inspections in manufacturing, following batch record instructions and current SOPs for documentation, visual inspections, testing intervals, and methods.
- Identify suspect material and perform segregation procedures as instructed or as specified in written instructions.
- Check batch documents for correct product, lot number, expiration dates, and components, and conduct on-line reviews.
- Perform AQL sampling and document inspection results in batch records.
- Perform LOTO, product inspections, line clearance duties, and shift-change line verification according to procedures.
- Pull in-process samples and deliver them as required.
- Interact with Materials Management, Contract Manufacturing, Engineering, and Validation; assist with and execute protocols and studies.
- Identify and notify relevant departments of potential or observed nonconformances.
- Assist Manufacturing with issuing, correcting, and reviewing batch documents.
- Assist Manufacturing with batch record reviews and batch record closure at the end of each run, including accountability and yield calculations.
- Complete required documentation reviews and work with Manufacturing to resolve outstanding issues before release to Quality Assurance.
- Evaluate quality issues and assist with investigations by providing necessary information and documentation.
- Support and participate in standardization and Quality metrics.
- Support manufacturing schedules and changes.
- Maintain awareness of and comply with GxP, ISO, and environmental health and safety procedures in the assigned area.
- Maintain compliance with GxP and procedural reading requirements, and pursue personal development.
- Train other Quality Control employees.
- Perform other duties as assigned.
Benefits
- The posting refers applicants to Bausch + Lomb's U.S. Benefit Programs but does not specify individual benefits.
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
High school or GED
