Technical Transfer Lead, GMP Manufacturing

Arrowhead Pharmaceuticals; Madison (WI); On-site; USD 90,000 - 115,000; Full time

Benefits offered by this job

Competitive salary

Excellent benefits

Job summary

Arrowhead Pharmaceuticals, Inc. is seeking a technically skilled professional to lead GMP technical transfer activities, writing and updating batch records, methods, and SOPs to ensure manufacturing readiness and effective transfer between process development and manufacturing teams in Madison, WI.

The role requires coordinating cross-functional teams, managing timelines, investigating deviations, and implementing CAPAs while maintaining controlled documentation and high attention to detail.

Qualifications

• BS/BA in an applicable scientific field such as chemistry, biology, or biochemistry.
• 3 years working in a GMP setting with a minimum of 1 year of experience in a technical writer or technical transfer position.
• Proficient experience working with controlled documentation.
• Experience with internal CAPA investigations.
• Ability to collaborate with and coordinate cross-functional teams.
• Proficiency with Microsoft Suite applications (Word, Excel).
• High attention to detail.
• Ability to multi-task and manage responsibilities within ongoing projects.

Responsibilities

• Work between process development and manufacturing scientists to create and maintain production batch records and process documentation.
• Facilitate cross-functional coordination and input to document new methods.
• Manage project timelines and provide project milestone updates to internal team members.
• Identify and implement best practices and process improvements to technical transfer activities and documentation.
• Lead deviation investigations and implement appropriate corrective action as necessary.
• Contribute to the compilation of master data.
• Write SOPs pertaining to GMP production.
• Perform reviews of executed batch records.
• Work with different departments to achieve project readiness goals.
• Occasionally assist with laboratory work as needed.

Skills

GMP documentation

Technical writing

Cross-functional coordination

Batch records

CAPA investigations

Project coordination

MS Excel

Education

BS/BA in chemistry/biology/biochemistry

Tools

Microsoft Word

Excel

Job description

Arrowhead Pharmaceuticals, Inc. is seeking a technically skilled professional to lead GMP technical transfer activities, writing and updating batch records, methods, and SOPs to ensure manufacturing readiness and effective transfer between process development and manufacturing teams in Madison, WI.

The role requires coordinating cross-functional teams, managing timelines, investigating deviations, and implementing CAPAs while maintaining controlled documentation and high attention to detail.