Process Equipment Validation Engineer

2 weeks ago

Los Angeles, California, United States Stark Pharma Solutions Inc Full time

Position:
Process Equipment Validation Engineer

Location:
Los Angeles, CA (Onsite)

Experience:
3 10 Years

Duration:
12+ Months

NOTE: Local candidates preferred
Position Overview
We're looking for a skilled
Process Equipment Validation Engineer
to support a long-term pharmaceutical facility project. This is a
Contract onsite role
requiring close coordination with construction and validation teams, as well as daily site walks in full PPE.

Key Responsibilities

  • Execute Facilities CQV activities, including EMPO, Vessel IOV, and IOPQ (mixing and temperature mapping).
  • Support commissioning and qualification of process equipment such as centrifuges, filter presses, and processing tanks.
  • Perform installation qualification (IQ) and operational qualification (OQ) of equipment and systems.
  • Conduct job walks at the construction site with engineering teams to monitor progress and compliance.
  • Collaborate with cross-functional teams to ensure project timelines and quality standards are met.
  • Generate, review, and maintain technical documentation for CQV deliverables.
  • Provide additional support for systems such as Utilities (WFI, Alcohol, N , Compressed Air), CIP, Filter Press, Centrifuge, and Cleaning Validation as needed.
  • Maintain high safety standards while performing daily activities in a regulated environment.

Qualifications

  • Bachelor's degree in Engineering or a related field.
  • 3 10 years of experience in Validation or CQV within the pharmaceutical industry.
  • Strong knowledge of facilities and process equipment validation.
  • Cleanroom qualification experience is a plus.
  • Excellent technical writing and documentation skills.
  • Strong communication, organization, and multitasking abilities.
  • Experience supporting capital projects and conducting job walks.
  • Must be flexible to support other shifts on short notice as required.

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