Piper Companies
Validation Engineer
Piper Companies, Lynwood, CA, United States
Piper Companies is currently seeking an experienced Validation Engineer tosupport a highly reputable Pharmaceutical company in Lynwood, California.
Responsibilities for the Validation Engineer
This job opens for applications on 1/9/2025. Applications for this job will be accepted for at least 30 days from the posting date.
Keywords: Validation, Validation Methodology, Packaging Validation, Cleaning Validation, 21 CFR, Pharmaceutical, IQ, OQ, PQ, QMS, Oracle, Technical Writing,
#LI-JM1 #LI-ONSITE
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.
- 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.
- Salary Range: $80,000-$95,000
- Comprehensive Benefits: Medical, Dental, Vision, 401K, PTO, Sick Leave as required by law, and Holidays
This job opens for applications on 1/9/2025. Applications for this job will be accepted for at least 30 days from the posting date.
Keywords: Validation, Validation Methodology, Packaging Validation, Cleaning Validation, 21 CFR, Pharmaceutical, IQ, OQ, PQ, QMS, Oracle, Technical Writing,
#LI-JM1 #LI-ONSITE