Manufacturing Support Lead — GMP Operations & Development

FUJIFILM Biotechnologies; Holly Springs (NC); On-site; USD 110,000 - 140,000; Full time

Benefits offered by this job

Competitive compensation

Comprehensive health benefits

Retirement plan options

Generous paid time off

Leadership development

Job summary

FUJIFILM Biotechnologies in Holly Springs, NC, seeks a Manager, Manufacturing Support to lead a talented team and ensure GMP-ready operations across a dynamic biopharma production environment. You will drive operational readiness, cross-functional collaboration, and continuous improvement, while guiding policy administration, training, and inspections readiness to support drug substance manufacturing.

This leadership role emphasizes people-first culture, accountability, and robust CAPA and

Qualifications

• High School diploma or GED with 10 years related experience
• Bachelor’s Degree with 6 years related experience
• Master’s Degree with 4 years of related experience

Responsibilities

• Provide oversight and lead operational readiness projects, including but not limited to GMP readiness
• Lead creation or transfer of manufacturing support team processes to ensure GMP readiness
• Manage, lead, and develop direct reports within the manufacturing support team
• Coordinate policy administration and time/expense reporting
• Coordinate non-batch activities and collaborate cross-functionally (CAPAs, investigations, batch schedules)
• Act as functional lead for regulatory inspections and audits
• Perform other duties as assigned

Skills

People leadership

GMP knowledge

Regulatory inspections

Project management

Cross-functional collaboration

Coaching

Education

Bachelor's Degree

Master's Degree

High School diploma or GED

Job description

FUJIFILM Biotechnologies in Holly Springs, NC, seeks a Manager, Manufacturing Support to lead a talented team and ensure GMP-ready operations across a dynamic biopharma production environment. You will drive operational readiness, cross-functional collaboration, and continuous improvement, while guiding policy administration, training, and inspections readiness to support drug substance manufacturing.

This leadership role emphasizes people-first culture, accountability, and robust CAPA and