Senior Sterile Liquids Process Engineer

Scorpion Therapeutics; Pennsylvania; On-site; USD 90,000 - 120,000; Full time

Benefits offered by this job

Annual bonus

Comprehensive benefits

Job summary

Scorpion Therapeutics in West Point, PA is seeking a Sr. Specialist, Engineering to provide technical input on sterile processes, oversee GMP-compliant manufacturing projects, and serve as the main interface with development scientists for clinical and development batches.

The role emphasizes deviations management, process improvement, and the introduction of new technologies within a highly regulated manufacturing environment.

Qualifications

• Bachelor’s degree in Chemical Engineering, Chemistry, Biology, or related scientific field.
• 3+ years in a technical or operations support role.
• Sterile process manufacturing and/or formulation development.
• Knowledge of manufacturing equipment and Good Manufacturing Practices (GMP).
• Project management, analytical problem-solving, cross-functional leadership.
• Technical writing (batch documentation, investigations, protocols).

Responsibilities

• Provide technical input on sterile processes from a facility/operational standpoint.
• Provide manufacturing project management oversight and GMP expertise to ensure timely availability of clinical supplies and development batches.
• Serve as the main interface with development scientists for manufacturing sterile liquid clinical and development batches.
• Manage deviations; lead process improvement projects.
• Implement new technologies and support process design.

Skills

Deviation management

Batch production records

Documentation preparation

Equipment qualification

Process development

Process optimization

Process hazard analysis

Analytical/data analysis

Problem identification

Education

Bachelor of Science in Chemical Engineering, Chemistry, Biology, or related scientific field

Tools

GMP knowledge

Job description

Scorpion Therapeutics in West Point, PA is seeking a Sr. Specialist, Engineering to provide technical input on sterile processes, oversee GMP-compliant manufacturing projects, and serve as the main interface with development scientists for clinical and development batches.

The role emphasizes deviations management, process improvement, and the introduction of new technologies within a highly regulated manufacturing environment.