Inspector- 1st Shift

Kindeva; Maryland Heights (MO); On-site; USD 42,000 - 62,000; Full time

Job summary

Kindeva is seeking a diligent Quality Inspector in Missouri to ensure batch record integrity, verify inspections, and maintain accurate documentation. The role requires strict adherence to SOPs, cGMPs, and departmental procedures, with hands-on testing of units and weight checks for fill accuracy.

You will also help keep the workspace clean and participate in process improvements to support product quality.

Qualifications

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

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 housekeeping duties to ensure a clean, orderly and safe workenvironment.
• Participate in process improvement activities.

Education

High school diploma / GED

Associate's degree in a science related discipline

Job description

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 housekeeping duties 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 related discipline.
• Pharmaceutical manufacturing experience preferred.