Validation Engineer
Lynwood, CA
Job Id:
144856
Job Category:
Job Location:
Lynwood, CA
Security Clearance:
No Clearance
Business Unit:
Piper Companies
Division:
Piper Clinical Solutions
Position Owner:
Kayla Torrey
Piper Companies is seeking a Validation Engineer to join a leading pharmaceutical manufacturing company located in Lynwood, Ca.
Responsibilities of the Validation Engineer include:
- Manage end to end, hands on, validation for products, processes, equipment and packaging
- Supports all qualification tasks related to manufacturing equipment – IQ/OQ/PQ
- Prepare, execute, and review validation protocols and documentation.
- Provide technical decisions on validation strategies and product disposition.
- Ensure GMP and FDA compliance; interface with regulators.
- Report to management and support cross-functional project teams.
Qualifications for the Senior Validation Engineer include:
- 5-7 years of experience in a similar liquid pharmaceutical industry role
- Knowledge of FDA guidance and Validation for process, equipment, and cleaning.
- Proficiency in Office 365, Oracle, QMS, statistical/validation tools
- Strong technical writing, verbal and written communication skills
- Ability to manage multiple tasks, work independently, and thrive in a fast-paced environment with changing priorities
- Bachelor's degree in chemical or Biological Sciences/Engineering required
Compensation for the Senior Validation Engineer include:
- Salary Range: $70-75,000 **Depending on experience**
- Comprehensive Benefits: Medical, Dental, Vision, 401K, PTO, Sick Leave if required by law, and Holidays
This job opens for applications on 7/1/2025. Applications for this job will be accepted for at least 30 days from the posting date.
Keywords: commissioning, qualification, decommissioning, production, validation standards, validation criteria, procedures, protocol, validation test equipment, detail-oriented, quality assurance, innovation, documentation, communication, collaboration, risk management, time management, GMP, problem solving, medical device, hardware, adaptability, technical writing, project management, FDA, Oracle, QMS, statistical tools , biological sciences, engineering, tests, instruments, quality director, quality engineer, supplier quality engineer, validation specialist
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