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Senior Validation Engineer
Barry-WehmillerSr. Validation Engineer supporting capital project CQV delivery in pharmaceutical environments.
About the role
Key responsibilities & impact- Assist basic and conceptual design phases of capital projects
- Establish User Requirement Specifications for critical equipment and systems
- Assess risk across various aspects of systems’ functions
- Develop and execute validation and FDA compliance related documents/protocols
- Prepare, execute, and manage commissioning and qualification documents
Requirements
What you’ll need- Minimum 7+ years demonstrated experience with design, commissioning, validation of automation
- Extensive hands-on experience with GMP-regulated environments
- Bachelor's degree in Engineering (Bioengineering, Biomedical, Chemical, Electrical, Mechanical, or equivalent technical degree)
- Proficiency with project documentation and computer skills (Microsoft Office, Microsoft Project, AutoCAD)
- Experience with entire project lifecycle from concept development through startup (preferred)
Benefits
Comp & perks- Professional development resources
- First Year Experience program
- Individual Development Plans
- Career Path resources and tools
ATS Keywords
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Hard Skills & Tools
designcommissioningvalidationrisk assessmentFDA complianceUser Requirement Specificationsproject lifecycle managementGMP regulations