Onsite Senior Manager, Manufacturing Technical Operations

Catalent Pharma Solutions; Glen Burnie (MD); On-site; USD 135,000 - 165,000; Full time

Benefits offered by this job

Medical, dental, and vision benefits

Tuition reimbursement

Paid time off

Job summary

Catalent Pharma Solutions is seeking a Manager, Manufacturing Technical Operations to lead the MTO group and ensure GMP-compliant operations at our Harmans, MD site. You will drive investigations, deviations, and continuous improvement while coordinating with technology transfer and cross-functional teams.

The role requires leadership, strong technical writing, and extensive GMP knowledge, with a Monday–Friday, 8am–5pm onsite schedule and a focus on performance and safety.

Qualifications

• Master’s degree in a Scientific, Engineering, or Biotech field with 6+ years of GMP experience.
• Bachelor’s degree in a Scientific, Engineering, or Biotech field with 8+ years of GMP experience.
• Minimum 3 years of progressive leadership experience and people development.
• Strong knowledge of GMP, FDA regulations, and documentation procedures.

Responsibilities

• Build and lead the Manufacturing Technical Operations group to support current and future operations.
• Interface with stakeholders and clients, ensuring on-time project completion and clear communication.
• Oversee investigations, deviations, CAPAs, and change controls with measurable results.
• Coordinate continuous improvement and operational excellence initiatives and project slate.
• Support technology transfer teams with manufacturing representation and data analytics.
• Oversee document generation, BOM management, scheduling, and suite readiness.

Skills

Leadership experience

Communication skills

GMP knowledge

Cross-functional collaboration

Technical writing

Project management

Education

Master’s degree in Scientific/Engineering/Biotech

Bachelor’s degree in Scientific/Engineering/Biotech

Job description

Catalent Pharma Solutions is seeking a Manager, Manufacturing Technical Operations to lead the MTO group and ensure GMP-compliant operations at our Harmans, MD site. You will drive investigations, deviations, and continuous improvement while coordinating with technology transfer and cross-functional teams.

The role requires leadership, strong technical writing, and extensive GMP knowledge, with a Monday–Friday, 8am–5pm onsite schedule and a focus on performance and safety.