Inspector

Kindeva; Maryland Heights, Northern (MO, KY); Hybrid; USD 42,000 - 55,000; Full time

Job summary

Kindeva in Missouri is seeking a quality-focused Manufacturing Associate to support pharmaceutical production and inspection workflows. You will strictly follow batch records, SOPs, and cGMPs, ensuring accurate documentation and traceability across all steps.

Ideal candidates have a GED or higher, at least one year of relevant experience or an associate’s degree in a science field, with pharmaceutical manufacturing experience preferred.

Qualifications

• High school diploma or GED.
• 1+ years relevant work experience or military experience or an 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 DepartmentalProcedures.
• 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.

Skills

Attention to detail

Quality inspection

Education

GED

Associate's degree in science

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 DepartmentalProcedures.
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.