Senior QA Label Control | 2nd Shift

Simtra US LLC; Bloomington, Northern (IN, KY); Hybrid; USD 58,000 - 78,000; Full time

Benefits offered by this job

Medical & Dental Coverage

401(k) Retirement Savings Plan with 2%

Paid Holidays

Paid Time Off

Job summary

Simtra BioPharma Solutions in Bloomington, Indiana is seeking a Sr. QA Inspector for Label Control on the 2nd shift. You will print, count, inspect, and issue client-specific printed materials for pharmaceutical products, ensuring first-pass quality under cGMP guidance.

The role requires at least a high school diploma, 2 years in pharma/biotech, and proficiency with MS Office and enterprise systems like D365, Veeva, ROBAR. Overtime, safety, and teamwork are emphasized.

Qualifications

• High School diploma or GED required.
• Minimum 2 years experience in a pharmaceutical or biotech industry required.
• General knowledge of Quality and Warehouse Operations is preferred.
• Computer proficiency in Microsoft Word, Excel, and Outlook and the ability to use enterprise software (examples include: D365, Veeva, ROBAR, etc.)

Responsibilities

• Print, count, inspect, and issue all client-specific printed materials for pharmaceutical products.
• Meet client demand with first pass quality using controlled documentation and cGMP guidelines.
• Ensure accuracy of inventory counts and participate in process improvements for Label Control.
• Act as the first point of contact for printer materials/Label Control issues and perform cycle counts in ERP.
• Perform QA Checklist Assessments to ensure compliance of all Finishing department areas.

Skills

Quality Assurance

Warehouse Operations

Communication

Education

High School diploma or GED

Tools

Microsoft Word

Microsoft Excel

Microsoft Outlook

D365

Veeva

ROBAR

Job description

Simtra BioPharma Solutions in Bloomington, Indiana is seeking a Sr. QA Inspector for Label Control on the 2nd shift. You will print, count, inspect, and issue client-specific printed materials for pharmaceutical products, ensuring first-pass quality under cGMP guidance.

The role requires at least a high school diploma, 2 years in pharma/biotech, and proficiency with MS Office and enterprise systems like D365, Veeva, ROBAR. Overtime, safety, and teamwork are emphasized.