Night Shift Manufacturing Manager – Biopharma Operations Leader

KBI Biopharma; Boulder (CO); On-site; USD 118,000 - 148,000; Full time

Job summary

KBI Biopharma is seeking a Manager, Manufacturing (Nights) to lead cGMP manufacturing operations on a 2x2x3 night rotation from 6:00 PM to 6:30 AM. You will manage daily production schedules, assign staff, and ensure compliant, high-quality output in a fast-paced biopharma environment.

The role requires a related scientific or engineering degree with 4+ years of leadership experience, and the ability to train personnel, review batch records, and uphold safety and quality standards while driving

Qualifications

• Bachelor’s degree in a related scientific or engineering discipline with 4+ years industry experience, or 10 years’ experience with high school diploma.
• 4+ years prior leadership/supervisory experience.
• Excellent written and verbal communication skills.
• Organized and able to work in a fast-paced, multi-tasked environment and maintain operational efficiency.
• Strong leadership, accountability, and conflict management capabilities.
• Willingness to work 12-hour night shifts.
• Experience in a cGMP manufacturing facility with clean room operations.

Responsibilities

• Execute manufacturing requirements to meet productivity, quality, and capacity objectives as set by management.
• Coordinate process improvements with quality and regulatory to ensure cGMP compliance.
• Hire, develop and motivate manufacturing operators; conduct performance reviews.
• Assist with production planning and scheduling.
• Maintain floor oversight with a KPI target of 80%.

Skills

Leadership

Team management

cGMP

Manufacturing operations

Communication skills

Problem solving

Education

Bachelor’s degree in related scientific/engineering field

High school diploma + 10 years’ experience

Job description

KBI Biopharma is seeking a Manager, Manufacturing (Nights) to lead cGMP manufacturing operations on a 2x2x3 night rotation from 6:00 PM to 6:30 AM. You will manage daily production schedules, assign staff, and ensure compliant, high-quality output in a fast-paced biopharma environment.

The role requires a related scientific or engineering degree with 4+ years of leadership experience, and the ability to train personnel, review batch records, and uphold safety and quality standards while driving