Night Shift Manufacturing Supervisor: Process & People

INCOG BioPharma Services; Fishers (IN); On-site; USD 70,000 - 110,000; Full time

Job summary

INCOG BioPharma Services is seeking a Manufacturing Supervisor to lead aseptic manufacturing operations on a 3rd shift (Sun–Thu, 11:00 PM–7:30 AM) in Fishers, Indiana. The role emphasizes schedule planning, batch record review, and team leadership to meet quality and regulatory standards.

You will coach operators, drive continuous improvement, and participate in deviation investigations, CAPA, and client audits, while aligning with company values and fostering career growth for team members.

Qualifications

• Knowledge of process control and quality engineering within aseptic manufacturing.
• Understanding of cGMP and related regulatory requirements.
• Experience leading teams and coaching operations staff.
• Familiarity with batch review, deviation investigations, and CAPA.

Responsibilities

• Batch and resource detail schedule planning.
• Provide floor support and real time batch record review.
• Provide technical support, oversight and team leadership in manufacturing batch activities.
• Coordinate development of individual team members with routine one on ones, training oversight and training opportunities.
• Develop and improve current processes to maintain and control the formulation and filling operations.
• Attend cross functional leadership meetings, support client audits and tours.
• Attend daily batch release and deviation triage meetings as representative for operations.
• Assure compliance with cGMP requirements (current good manufacturing practices).
• Perform GEMBA walks and checks for process improvements.

Skills

Process control

Quality engineering

cGMP knowledge

Aseptic processing

Statistical methods

Communication skills

Leadership experience

Job description

INCOG BioPharma Services is seeking a Manufacturing Supervisor to lead aseptic manufacturing operations on a 3rd shift (Sun–Thu, 11:00 PM–7:30 AM) in Fishers, Indiana. The role emphasizes schedule planning, batch record review, and team leadership to meet quality and regulatory standards.

You will coach operators, drive continuous improvement, and participate in deviation investigations, CAPA, and client audits, while aligning with company values and fostering career growth for team members.