PolyPeptide US-posted 8 days ago
$98,000 - $112,000/Yr
Full-time • Entry Level
Torrance, CA
1,001-5,000 employees

Join PolyPeptide as a Validation Engineer and help ensure the quality and reliability of equipment and processes used to manufacture life-changing peptide therapeutics. If you’re an early-career engineer ready to grow in a fast-paced, cGMP environment, this role is a great fit.

  • Develop and review URS for new and existing equipment.
  • Plan and execute IQ/OQ/PQ qualifications.
  • Support process and cleaning validations.
  • Create and maintain validation protocols, reports, and SOPs.
  • Investigate deviations and support CAPA activities.
  • Collaborate with Quality, Manufacturing, and Process Development teams.
  • Assist with scale-up and tech transfer of validated processes.
  • Bachelor’s degree in Engineering, Chemistry, or related field.
  • 1–3 years of experience in validation, quality, or manufacturing in a cGMP setting.
  • Understanding of validation principles and pharmaceutical processes.
  • Strong documentation, communication, and problem-solving skills.
  • Detail-oriented mindset and ability to manage multiple priorities.
  • Join a growing global CDMO where your work directly supports product quality and patient safety.
  • You’ll gain hands-on experience, cross-functional exposure, and the opportunity to make a real impact.
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