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 plusFlexible 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 HolidaysThis 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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