Inspector- 2nd Shift

Kindeva

Maryland Heights (MO)

Hybrid

USD 32.000 - 45.000

Vollzeit

14 Tage+

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Zusammenfassung

Kindeva in Missouri seeks a detail-oriented Quality Inspector to support batch record compliance and ensure product integrity. You will follow SOPs, cGMPs, and departmental procedures while inspecting units for defects and verifying fill volumes.

The role emphasizes accurate record-keeping, adherence to quality standards, and participation in process improvements within a collaborative manufacturing team.

Qualifikationen

  • High school diploma or GED is required for this role.
  • 1+ years relevant work experience or Veterans / Military experience or an associate’s degree in a science related discipline is required.
  • Pharmaceutical manufacturing experience is preferred.

Aufgaben

  • Strict adherence to batch record instructions, SOPs, cGMPs and departmental procedures.
  • Qualify on manual and automated inspection systems.
  • Visually inspect units for defects.
  • Weight checks basic units for correct fill volume.
  • Maintain accountability records (talliesheets, label preparation, batch record information, etc.).
  • Perform housekeeping duties to ensure a clean, orderly and safe work environment.
  • Participate in process improvement activities.

Ausbildung

High school diploma / GED
Associate’s degree in a science related discipline

Jobbeschreibung

Our Work Matters

At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world.

Role Responsibilities
  • Strict adherence to all batch record instructions, SOP’s, cGMP’s and all applicable Departmental Procedures.
  • Qualify on manual and automated inspectionsystems.
  • Visually inspect units for defects.
  • Weight checks basic units for correct fill volume.
  • Maintain proper accountability records (i.e. tallysheets, label preparation, batch record information,etc.)
  • Perform appropriate departmental housekeepingduties to ensure a clean, orderly and safe workenvironment.
  • Participate in process improvement activities.
Qualifications
  • High school diploma / general education degree (GED)
  • 1+ years relevant work experience or Veterans / Militaryexperience or associate’s degree in a science relateddiscipline.
  • Pharmaceutical manufacturing experience preferred.
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