Senior Manager, Quality Validation – GMP/Commercial

Scorpion Therapeutics

California (MO)

On-site

USD 164,000 - 205,000

Full time

11 days ago
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Job summary

Scorpion Therapeutics, a late-stage oncology biopharma, seeks a Senior Manager, Quality Validation to oversee commercial manufacturing validation activities. The role focuses on PPQ and CPV, liaising with CMOs for drug substance, drug product, and packaging.

You will drive compliance with global GMP standards and support regulatory readiness. Responsibilities include reviewing validation plans and risk assessments, monitoring metrics, and guiding investigations and change controls to ensure a

Qualifications

  • 8+ years in GMP pharmaceutical quality and manufacturing.
  • Proven experience in validation lifecycle, especially PPQ and CPV.
  • Knowledge of process validation principles and global GMP regulations.
  • Experience supporting commercial product lifecycle.

Responsibilities

  • Oversee validation activities including PPQ and CPV across CMOs for drug substance, product, and packaging.
  • Review validation plans, reports, and risk assessments.
  • Ensure compliance with global GMP standards.
  • Support GMP operations, deviations, investigations, and change controls.
  • Monitor validation metrics and assist regulatory inspection readiness.

Skills

Validation lifecycle
GMP knowledge
Regulatory compliance
Cross-functional collaboration

Education

Bachelor's degree in science/engineering/technical field

Job description

Scorpion Therapeutics, a late-stage oncology biopharma, seeks a Senior Manager, Quality Validation to oversee commercial manufacturing validation activities. The role focuses on PPQ and CPV, liaising with CMOs for drug substance, drug product, and packaging.

You will drive compliance with global GMP standards and support regulatory readiness. Responsibilities include reviewing validation plans and risk assessments, monitoring metrics, and guiding investigations and change controls to ensure a

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