Katalyst CRO

Process Validation Engineer

Swiftwater, PA, US

about 1 month ago
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Summary

Roles & Responsibilities

  • Bachelor's degree in science or engineering (MS accepted, PhD is overqualified).
  • Minimum 2+ years in Process Validation within the biotech/pharma industry.
  • Writing and executing process validation documents.
  • Strong Process Performance Qualification (PPQ) experience.
  • Hands-on experience collecting process samples.
  • Must have on-the-floor manufacturing experience.
  • Familiarity with GMP best practices.
  • Proficient in MS Office (Word, Excel, PowerPoint).
  • Strong written and verbal communication skills in English.
  • Ability to work independently and reliably.
  • Candidates must gown up for the role.
  • Not a computer validation role - hands-on process validation experience required.
  • Candidates must provide two professional references (Manager Name, Title, Work Email, and Phone Number) upon submission.

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