Process Equipment Validation Engineer

Process Equipment Validation Engineer

Join to apply for the Process Equipment Validation Engineer role at Stark Pharma Solutions Inc . We are looking for a skilled engineer to support a long-term pharmaceutical facility project. This is a contract onsite role requiring close coordination with construction and validation teams, and daily site walks in full PPE.

Location : Los Angeles, CA (Onsite)

Experience : 3-10 Years

Duration : 12+ months

NOTE : Local candidates preferred

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

J-18808-Ljbffr