Aseptic QA Supervisor – 2nd Shift Leader

Kindeva; Brentwood (MO); On-site; USD 85,000 - 110,000; Full time

Job summary

Kindeva is seeking a QA Supervisor – Aseptic to oversee Quality Inspector colleagues in the Sterile Product Manufacturing (SPM) building. You will apply GDP, GMP and aseptic processing knowledge to resolve deviations and support regulatory compliance.

This 2nd shift (2pm–10:30pm), onsite role requires leadership of QA staff, training, batch record review, and daily shift reporting. Strong collaboration with Production and QA Management is essential.

Qualifications

• Minimum 3 years of pharmaceutical experience or equivalent combination of education and experience.
• Experience at an aseptic manufacturing site is preferred.
• 1 year of supervisory experience is preferred.

Responsibilities

• Oversee QA inspectors and ensure adequate coverage through dynamic scheduling for APA and Grade D/CNC areas throughout the shift.
• Ensure training is completed for direct reports.
• Generate daily written shift reports for Quality and Production Management with clear details of relevant issues.
• Lead investigations and contribute to Root Cause Analysis and preventive actions for manufacturing deviations.

Skills

Aseptic QA knowledge

Supervisory experience

GMP/GDP compliance

Batch record review

Team leadership

Education

Bachelor's degree in science

Associate degree + 2+ years experience

Job description

Kindeva is seeking a QA Supervisor – Aseptic to oversee Quality Inspector colleagues in the Sterile Product Manufacturing (SPM) building. You will apply GDP, GMP and aseptic processing knowledge to resolve deviations and support regulatory compliance.

This 2nd shift (2pm–10:30pm), onsite role requires leadership of QA staff, training, batch record review, and daily shift reporting. Strong collaboration with Production and QA Management is essential.