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
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.J-18808-Ljbffr