Senior QA Inspector – Line Operations (Night Shift)

Simtra BioPharma Solutions

Bloomington (IN)

On-site

USD 65,000 - 90,000

Full time

24 hours ago
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Benefits offered by this job

Medical & Dental Coverage
401(k) with Company Match
Paid Holidays
Paid Time Off
Adoption Reimbursement
Education Assistance
Employee Ownership Plan

Job summary

Simtra BioPharma Solutions in Bloomington, IN, is seeking a Sr. Quality Inspector (Line Operations) to ensure acceptable quality levels (AQL) for all GMP products on finishing lines. The role emphasizes risk-based quality decisions, teamwork, safety, and adherence to SISPQ in a fast-paced manufacturing environment.

Working hours are Monday–Friday, 10:45 PM–6:45 AM, with potential overtime. Ideal candidates have GMP experience, strong attention to detail, and proficiency with enterprise software

Qualifications

  • High School diploma or GED required.
  • Minimum 2 years of experience in a pharmaceutical or biotech industry.
  • Must be able to use Microsoft Word, Excel, and Outlook and enterprise software (examples include D365, Veeva, ROBAR).
  • Must be able to lift 50 lbs and pass vision/color tests.
  • Overtime and weekend work may be required.

Responsibilities

  • Monitor product quality through AQL inspections.
  • Perform unit and packaging level visual inspections to ensure conformance with specifications.
  • Perform AQL sampling calculations based on ANSI Standards.
  • Provide QA support on production lines.
  • Cross-train in QA Label Control and QA Warehouse Technician tasks.

Skills

Attention to detail
Quality inspections
Safety compliance

Education

High School diploma or GED

Tools

Microsoft Word
Microsoft Excel
Microsoft Outlook
D365
Veeva
ROBAR

Job description

Simtra BioPharma Solutions in Bloomington, IN, is seeking a Sr. Quality Inspector (Line Operations) to ensure acceptable quality levels (AQL) for all GMP products on finishing lines. The role emphasizes risk-based quality decisions, teamwork, safety, and adherence to SISPQ in a fast-paced manufacturing environment.

Working hours are Monday–Friday, 10:45 PM–6:45 AM, with potential overtime. Ideal candidates have GMP experience, strong attention to detail, and proficiency with enterprise software

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