Validation Engineer

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

Responsibilities for the Validation Engineer

• 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.

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 , 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.

Compensation for the Validation Engineer

• Salary Range: $,-$,
• Comprehensive Benefits: Medical, Dental, Vision, K, PTO, Sick Leave as required by law, and Holidays

This job opens for applications on 5/5/5. Applications for this job will be accepted for at least days from the posting date.

Keywords: Validation, Validation Methodology, Packaging Validation, Cleaning Validation, CFR, Pharmaceutical, IQ, OQ, PQ, QMS, Oracle, Technical Writing,

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