Sterile Production Supervisor – Second Shift Leader

Kindeva; Brentwood (MO); On-site; USD 70,000 - 100,000; Full time

Job summary

Kindeva in St. Louis, MO, is seeking a Production Supervisor to lead sterile manufacturing operations, oversee daily activities, and guide a team of operators in a cGMP environment.

This second shift role emphasizes safety, quality, and continuous improvement, with collaboration across Quality, Engineering, Maintenance, Planning, and Supply Chain to meet production goals and maintain schedules.

Qualifications

• Minimum two years of supervisory experience in manufacturing, or ten+ years in pharma in lieu of degree.
• Proficiency with Microsoft Office, Kronos, and Veeva.
• Onsite work required; ability to manage multiple priorities.
• Strong written and verbal communication and leadership abilities.

Responsibilities

• Directly supervise production personnel and Lead Operators.
• Manage staffing, scheduling, attendance, vacations, and overtime.
• Interview, hire, onboard, train, coach, mentor, and develop employees.
• Conduct performance evaluations and administer corrective action when appropriate.
• Ensure employees maintain required qualifications, certifications, and training.
• Lead daily production meetings promoting accountability, teamwork, safety, quality, and continuous improvement.
• Support employee relations and labor relations activities, including union environments when applicable.
• Lead daily aseptic manufacturing operations and ensure production schedule attainment.
• Coordinate manufacturing activities to support production goals and customer commitments.

Skills

Leadership

Communication

Problem solving

Coaching

Team development

Education

Associate degree in scientific/technical/manufacturing/engineering or related field

Ten years of supervisory experience in pharmaceutical operations in lieu of degree

Tools

Microsoft Office

Kronos

Veeva

Job description

Kindeva in St. Louis, MO, is seeking a Production Supervisor to lead sterile manufacturing operations, oversee daily activities, and guide a team of operators in a cGMP environment.

This second shift role emphasizes safety, quality, and continuous improvement, with collaboration across Quality, Engineering, Maintenance, Planning, and Supply Chain to meet production goals and maintain schedules.