Biopharma Process Engineer — Cell Culture & Purification

Scorpion Therapeutics; Brooklyn Park (MN); On-site; USD 85,000 - 120,000; Full time

Job summary

Scorpion Therapeutics is seeking an engineering SME to support biopharmaceutical manufacturing processes, including cell culture, harvest, purification, and utilities. You will own system life cycles, develop PFDs and P&IDs, and lead modifications from design through commissioning.

Responsibilities cover FATs, CAPA investigations, asset management, and project execution within a strict cGMP and GEP framework.

Qualifications

• Bachelor's degree in Engineering (Chemical preferred).
• 0+ years of engineering experience in regulated biopharma or biotech manufacturing.
• Familiarity with bioreactors, chromatography, CIP, HVAC, and automation systems.
• Knowledge of GMP and industry best practices.

Responsibilities

• Oversee system lifecycle from design, qualification, to maintenance.
• Develop engineering deliverables (PFDs, P&IDs, specifications).
• Lead system modifications, FATs, commissioning, and CAPA investigations.
• Support system qualification, asset management, and project execution.
• Ensure compliance with cGMP and GEP standards; potentially serve as project manager for small capital projects.

Skills

Biopharma manufacturing

CIP

GMP knowledge

MS Office

Project management tools

Education

Bachelor's degree in Engineering (Chemical preferred)

Tools

PFDs & P&IDs

Job description

Scorpion Therapeutics is seeking an engineering SME to support biopharmaceutical manufacturing processes, including cell culture, harvest, purification, and utilities. You will own system life cycles, develop PFDs and P&IDs, and lead modifications from design through commissioning.

Responsibilities cover FATs, CAPA investigations, asset management, and project execution within a strict cGMP and GEP framework.