Supervisor, Production Operations 2nd Shift

Our Work Matters

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

• Purpose‑driven work environment
• Significant growth opportunities
• Collaborative, team‑oriented culture
• Direct impact on patient care
• Industry‑leading pharmaceutical innovation

Lead the production of life‑saving therapies.

As a Production Supervisor, you will provide leadership for our Sterile Production Manufacturing (SPM) operations, overseeing daily manufacturing activities while leading a team of production operators in a regulated pharmaceutical environment. You will ensure production schedules are achieved while maintaining the highest standards of quality, safety, and current Good Manufacturing Practices (cGMP).

Working closely with Quality, Engineering, Maintenance, Planning, and Supply Chain, you will help drive operational excellence, develop employees, and support the production of therapies that improve the lives of patients around the world.

Our St. Louis manufacturing operations continue to grow, creating exciting opportunities for Production Supervisors to lead high‑performing teams in a fast‑paced pharmaceutical manufacturing environment. Join us during this exciting period of growth and help build a culture focused on safety, quality, operational excellence, and continuous improvement.

This is a Second shift position.

• 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 while 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.
• Supervise Sterile Production Manufacturing (SPM) operations while ensuring production activities are completed safely, efficiently, and in compliance with established procedures.
• Coordinate manufacturing activities to support production goals and customer commitments.
• Support operational readiness and timely execution of manufacturing activities.
• Perform other duties as assigned.

• Ensure compliance with current Good Manufacturing Practices (cGMP), Standard Operating Procedures (SOPs), site safety requirements, and applicable regulatory expectations.
• Review production documentation for accuracy and completeness.
• Investigate deviations, quality events, and manufacturing issues while driving timely resolution.
• Support audits of aseptic manufacturing processes and supporting operations.
• Maintain compliance with documentation requirements and regulatory expectations.

• Drive continuous improvement initiatives focused on safety, quality, productivity, and operational performance.
• Identify opportunities to improve manufacturing processes and eliminate waste.
• Support operational excellence initiatives and promote a culture of continuous improvement.

• Partner closely with Quality, Engineering, Maintenance, Planning, and Supply Chain to support manufacturing operations.
• Collaborate with site leadership to resolve operational issues and achieve production objectives.
• Foster strong communication across departments to ensure safe, compliant, and efficient manufacturing operations.

• Required:
  
  Associate degree in a scientific, technical, manufacturing, business, engineering, or related field and a minimum of two (2) years of supervisory experience in a manufacturing environment; OR a minimum of ten (10) years of supervisory experience in pharmaceutical operations in lieu of a degree.
• Preferred:
  Pharmaceutical and/or manufacturing experience, experience in…