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Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in developing and executing Validation Master Plans (VMP) and process validation protocols (IQ/OQ/PQ) within the medical device industry. Proficient in documentation practices including quality plans, work instructions, and testing protocols.
Highest-signal resume keywords
Validation Master Plan DevelopmentProcess Validation (IQ/OQ/PQ)Documentation SkillsBachelor's Degree in Quality EngineeringMedical Device Experience
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Process ValidationValidation Master PlanProtocol DevelopmentQuality PlansWork InstructionsQuality InspectionTestingDocumentation
Industry Keywords
Medical DeviceQuality EngineeringValidation Engineering
About the role
Key responsibilities & impact- Support a customer team by providing engineering support to develop and execute IQ/OQ/PQ process validation
- Develop Validation Master Plan (VMP)
- Develop protocols and supporting documents
- Execute process validation (IQ, OQ, PQ)
- Complete documentation including protocols, IQ/OQ/PQ, quality plans, work instructions, label masters, quality inspection, and testing
- Work 40 hours per week for 8 weeks and go onsite in Grand Rapids as needed
Requirements
What you’ll need- Bachelor's degree in Quality Engineering, Validation Engineering, or a related Engineering degree
- Experience developing VMP's
- Experience developing validation process (IQ/OQ/PQ)
- Ability to document protocols, Process validation, quality plan, work instructions, etc.
- Work onsite in Grand Rapids as needed
- 1-5 years of medical device experienced preferred
Benefits
Comp & perks- 40 hour week for 8 weeks
- Potential contract extension
