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Validation Manager

Integrated Resources, Inc

Hercules, California

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JOB DETAILS
JOB TYPE
Full-time
SKILLS
Automation, Change Control, Clinical Research, Communication Skills, Corrective Action, Cross-Functional, FDA (Food and Drug Administration), FDA Requirements, Field Trials, Information Technology & Information Systems, Leadership, Medical Equipment, Microsoft Excel, Microsoft Office, Microsoft PowerPoint, Microsoft Word, Minitab, Multitasking, Physical Science, Presentation/Verbal Skills, Project Planning, Quality Assurance Methodology, Quality Metrics, Rehabilitation Nursing, Reliability Engineering, Reliability Testing, Requirements Management, Requirements Validation/Verification, Risk Analysis, Robotics, Root Cause Analysis, Six Sigma Green Belt, Statistical Analysis System (SAS), Statistics, Statistics Software, Team Player, Technical Support, Technical/Engineering Design, Test Data, Testing, Validation Plan, Validation Testing, Verification Engineering, Writing Skills
LOCATION
Hercules, California
POSTED
2 days ago
Validation ManagerA Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.Job DescriptionPosition: Validation ManagerLocation: Hercules, CADuration: Full timeLead Engineering Verification and Validation Activities managing a small contingent of validation engineers.• Serve as Subject Matter Expert (SME) for all verification and validation activities• Develop and oversee verification protocols to verify engineering specifications• Develop and oversee validation protocols to validate customer requirements• Analyze verification and validation test data• Document test protocols and reports• Support Root Cause Analyses and Develop Corrective Measureso Conduct root cause analysis using test data and/or field failure datao Develop and verify/validate effective countermeasures against root cause(s) of failure• Support Reliability Improvement Projectso Apply methodologies to drive reliability improvementso Develop and execute reliability test methods• Support Change Control Process• Support Engineering Design ReviewsRequired Skills• An understanding/working knowledge of Fluidics/Filling Operations, Automation, Robotics, Cold Storage, Packaging, and site validation. DI Water Systems• Highly proficient in the use of MS Office Suite (Word, Excel, Power-point, Project)• Proficient in the use of Minitab and/or other statistical analysis software• Excellent written and verbal communication skills• Ability to work effectively in teams – cross-functionally and within engineering• Ability to multitask effectively and efficiently• Ability to work effectively with general direction• Highly capable of independent and critical thought and actionRequired Experience• BS/MS in an Engineering discipline or Physical Sciences• Six Sigma Green Belt (preferred)• Test Implementation, Verification & Validation, and Risk Assessment• Root Cause Analysis, Development of Corrective Actions• Hands on application of Statistical Analysis• Working knowledge of FDA regulatory requirements and all internal quality standards• 5-7 years of experience in medical device validation/FDA regulated industry.• 3-5 years of management leadership experience• Project planning skills

About the Company

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Integrated Resources, Inc