Biologics External Manufacturing Engineering Lead

Scorpion Therapeutics

Pennsylvania

On-site

USD 120,000 - 160,000

Full time

3 days ago
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Benefits offered by this job

Travel 25%

Job summary

Scorpion Therapeutics seeks a Senior Specialist in Engineering for Biologics External Manufacturing Technical Operations to lead drug substance tech transfer and commercial production within the external manufacturing network. You will act as the primary interface with external partner drug substance manufacturers, author GMP documentation, drive process improvements, and support regulatory inspections.

This role emphasizes GMP compliance and inspection readiness, with a focus on standardized

Qualifications

  • Bachelor's degree in a chemical/biochemical engineering, pharmaceutical science, chemistry, or related field.
  • 8+ years post-bachelor GMP experience in operations, engineering, or technical support.
  • Strong problem-solving, communication, and organizational skills.
  • Ability to work independently and multi-task under tight deadlines.

Responsibilities

  • Lead technical transfer activities in biologics external manufacturing.
  • Serve as primary interface with external partner drug substance manufacturers.
  • Author and review GMP documentation.
  • Manage process improvements and support regulatory inspections.
  • Ensure external partners meet GMP compliance and inspection readiness.
  • Develop standardized work and drive continuous technical excellence.

Education

Bachelor's degree in Chemical/Biochemical Engineering, Pharmaceutical Science, Chemistry, or related field

Job description

Scorpion Therapeutics seeks a Senior Specialist in Engineering for Biologics External Manufacturing Technical Operations to lead drug substance tech transfer and commercial production within the external manufacturing network. You will act as the primary interface with external partner drug substance manufacturers, author GMP documentation, drive process improvements, and support regulatory inspections.

This role emphasizes GMP compliance and inspection readiness, with a focus on standardized

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