Piper Companies is currently seeking an experienced Validation Engineer to support a highly reputable Pharmaceutical company in Lynwood, California.

QUALIFICATIONS FOR THE VALIDATION ENGINEER

• Bachelor’s in Chemical/Biological Sciences or Engineering and 3+ years in liquid pharmaceutical roles required.
• Strong expertise in FDA process validation guidelines, validation methodology, and related technical disciplines (QC, QA, Engineering, Regulatory).
• Proficient in technical writing, Office 365, and statistical tools, with Oracle and QMS experience preferred.
• Skilled in time management, multitasking, and collaboration across cross-functional teams at all levels.
• Cleaning Validation Experience a plus
• Flexible to work off-shifts, weekends, holidays, and travel for validation support.

• Oversee validation activities, including risk analysis, packaging, cleaning, and equipment qualification for new and updated processes.
• Develop, review, and execute validation protocols, reports, and documentation while ensuring compliance with GMP standards.
• Coordinate validation efforts across shifts, providing technical guidance and resolving product or equipment issues.
• Support regulatory inspections and maintain communication with departments and the Corporate Validation Manager.
• Participate in projects and perform additional duties as assigned.