Technical Transfer Lead — GMP Documentation & Projects

Socket.dev; Verona (WI); On-site; USD 85,000 - 98,000; Full time

Benefits offered by this job

Excellent benefits

Job summary

Arrowhead Pharmaceuticals, Inc. is seeking a GMP technical transfer specialist to lead doc development and transfer activities between process development and manufacturing.

You will craft batch records, SOPs, and related GMP documents while coordinating across multiple teams to ensure readiness for new and existing programs. The role requires a BS/BA in a scientific field and 3+ years in GMP settings with tech transfer experience.

Qualifications

• BS/BA in chemistry, biology or biochemistry required.
• 3 years GMP experience with at least 1 year in technical writer or tech transfer.
• Proficient with controlled documentation and CAPA investigations.

Responsibilities

• Lead technical transfer activities to support manufacturing readiness.
• Write and develop GMP batch records, methods, and SOPs.
• Coordinate process transfer activities across cross-functional teams.
• Manage project timelines and provide milestone updates.
• Lead deviation investigations and implement corrective actions.
• Compile master data and review executed batch records.
• Collaborate with departments to achieve project readiness goals.
• Occasionally assist with laboratory work as needed.

Skills

Cross-functional collaboration

Project management

Attention to detail

GMP documentation

Microsoft Word/Excel

Education

BS/BA in chemistry, biology, or biochemistry

Tools

Microsoft Word

Microsoft Excel

Job description

Arrowhead Pharmaceuticals, Inc. is seeking a GMP technical transfer specialist to lead doc development and transfer activities between process development and manufacturing.

You will craft batch records, SOPs, and related GMP documents while coordinating across multiple teams to ensure readiness for new and existing programs. The role requires a BS/BA in a scientific field and 3+ years in GMP settings with tech transfer experience.