Pharma QA Inspector – 3rd Shift

ACTalent; Bohemia (NY); On-site; USD 33,000 - 40,000; Full time

Benefits offered by this job

Medical, dental & vision

401(k) Retirement Plan

Paid time off

Job summary

Actalent is seeking a QA Inspector to join our clinical label manufacturing team in Bohemia, NY. You will perform visual and automated inspections at multiple stages, ensuring labels meet specifications and regulatory standards.

The role requires documenting results and reporting trends to supervision. Ideal candidates have at least 1 year in QA/QC in a cGMP setting, experience with automated inspection equipment, and a keen eye for detail.

Qualifications

• Minimum 1 year of QA/QC experience in a regulated environment.
• Experience in a cGMP environment is required.
• Strong attention to detail and accuracy in inspections.
• Proficient in documenting inspection results and records.
• Troubleshooting skills for inspection processes.
• Ability to work in a fast-paced, team-oriented manufacturing environment.
• High school diploma or equivalent.

Responsibilities

• Perform visual and automated quality inspections at multiple stages throughout the manufacturing process.
• Inspect pharmaceutical labels for accuracy, legibility, alignment, print quality, and regulatory compliance.
• Set up, monitor, and perform routine checks on automatic inspection equipment.
• Identify defects, non-conformities, and deviations from specifications in labels and production materials.
• Document inspection results clearly and accurately, and maintain complete and organized quality records.
• Report quality issues, inspection findings, and trends promptly to supervision or management.
• Troubleshoot inspection issues and assist in identifying root causes and corrective actions.
• Maintain production pace while ensuring quality standards and regulatory requirements are met.

Tools

Automated inspection equipment

Job description

Actalent is seeking a QA Inspector to join our clinical label manufacturing team in Bohemia, NY. You will perform visual and automated inspections at multiple stages, ensuring labels meet specifications and regulatory standards.

The role requires documenting results and reporting trends to supervision. Ideal candidates have at least 1 year in QA/QC in a cGMP setting, experience with automated inspection equipment, and a keen eye for detail.