Lead, Technical Transfer

Scorpion Therapeutics; Madison (WI); On-site; USD 120,000 - 180,000; Full time

Job summary

Scorpion Therapeutics in Wisconsin is seeking a Lead to drive GMP technical transfer activities, ensuring seamless transition of RNAi-based therapeutics from development to manufacturing. The role focuses on coordinating cross-functional teams, maintaining documentation, and ensuring manufacturing readiness.

You will develop and maintain GMP batch records, methods, and SOPs; coordinate process transfer with engineering, QA, and manufacturing; manage timelines; lead deviation investigations; and

Qualifications

• BS/BA in chemistry, biology, or biochemistry required.
• Minimum 3 years GMP experience with at least 1 year in technical writing or transfer.
• Proficiency with controlled documentation and CAPA investigations.
• Strong project management skills and attention to detail.

Responsibilities

• Develop and maintain GMP batch records, methods, and SOPs.
• Facilitate cross-functional coordination for process transfer.
• Manage project timelines and milestones.
• Lead deviation investigations and implement corrective actions.
• Assist with laboratory work as needed.

Skills

GMP experience

Technical writing

Process transfer

CAPA investigations

Project management

Microsoft Office

Attention to detail

Multitasking

Cross-functional coordination

Education

BS/BA in chemistry, biology, or biochemistry

Job description

Role:

Lead technical transfer activities to support manufacturing readiness for GMP production of RNAi-based therapeutics, ensuring seamless process transfer from development to manufacturing.

Responsibilities:

• develop and maintain GMP batch records, methods, and SOPs;
• facilitate cross-functional coordination for process transfer;
• manage project timelines and milestones;
• lead deviation investigations and implement corrective actions;
• assist with laboratory work as needed.

Requirements:

• BS/BA in chemistry, biology, or biochemistry;
• minimum 3 years GMP experience, with at least 1 year in technical writing or transfer;
• proficient with controlled documentation, CAPA investigations, project management, and Microsoft Office;
• high attention to detail and multitasking ability.

Preferred:

5+ years GMP experience and 3+ years in technical transfer.

High-Value:

biopharma manufacturing, RNAi therapeutics, GMP batch documentation, process transfer, deviation investigations, cross-functional collaboration.

Work setup:

not specified; based in Wisconsin with competitive salary range.