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validation engineer
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Validation Engineer
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Jobot Ansonia, United StatesJob Description · Job DescriptionValidation Engineer - (Responsive) · This Jobot Job is hosted by: David Six · Are you a fit? Easy Apply now by clicking the "Apply Now" buttonand sending us your resume. · Salary: $80,000 - $90,000 per year · A bit about us: · Are you a dynamic, d ...
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Validation Engineer
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Jobot Ansonia, United StatesValidation Engineer - (Responsive) · Are you ready to apply Make sure you understand all the responsibilities and tasks associated with this role before proceeding. · This Jobot Job is hosted by: David Six · Are you a fit? Easy Apply now by clicking the "Apply" button · and s ...
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Validation Engineer
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Jobot Ansonia, United StatesValidation Engineer - (Responsive) This Jobot Job is hosted by: David Six Are you a fit? Easy Apply now by clicking the "Apply" button and sending us your resume. Salary: $80,000 - $90,000 per year A bit about us: Are you a dynamic, detail-oriented engineer with a passion for pro ...
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Validation Engineer
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Validation Engineer
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Manufacturing validation engineer
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Syntricate Technologies North Haven, United StatesHi,We are looking for a Manufacturing Validation Engineer. Please let me know, if interested.Manufacturing validation engineerNorth Haven, CTFull Time/ContractJob duties: Process and equipment qualification (IQ/OQ/PQ). Development of test methods for Design V&V, Process Validatio ...
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Manufacturing validation engineer
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Engineer III, Validation
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Silicon Validation Engineer
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Software Test Validation Engineer
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Manufacturing Validation Engineer - Shelton, United States - Katalyst Healthcares and Life Sciences
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Description
Responsibilities:
Experience in supporting medical device manufacturing.
Specific experience with process characterization, equipment IQ/OQ, process OQ, and PQ Validation Experience, especially cleaning Processes experience, molding, cleaning, packaging Specific experience with Test method Validation and Gage R&R Experience with root cause analysis and problem-solving for both technical and process issues Working knowledge of design control and cGMP requirements for medical device manufacturing per FDA QSR and ISO bility to lead and prioritize multiple medium-complexity project assignments and complete work in a timely manner.
Good problem-solving skills through the use of quality and statistical tools, Six Sigma bility to read and understand engineering drawings.
Knowledge of basic quality tools, risk analysis (PFMEA), statistics (SPC), Critical-to Quality (CTQ) Analysis Knowledge of Quality System requirements, ISO and FDA requirements bility to effectively work within a cross-functional team to complete critical project tasks.
Demonstrates good written and verbal communication skills.Experienced with control procedures, such as the Change Management System, Nonconformance Reports, Engineering Specifications, Corrective and Preventive Action (CAPA), and Work Instructions and proficient with Statistical Process Control concepts, process development, CNC programming terminology, and tooling design concepts.
Microsoft Office Suite and Project