Process Quality Engineer at ST Global Tech LLC | Torre

Process Quality Engineer

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Full-time

Legal agreement: Contractor

Currency exchange and payroll taxes to be paid by:

Company

Compensation
GBP22 - 25/hour
~USD29.7 - 33.8/hour
Non-negotiable
location_on
Leeds, England, United Kingdom
Posted 15 days ago

Responsibilities


Job Role : Process Quality Engineer Work Location – Leeds, UK Mode of Hiring- Permanent No. of positions: 2 Qualification-BE/B.tech - Mechanical/Production/Bio-Medical Experience: 3+ years relevant experience 5 Days Onsite Rates- 22-25 GBP Per Hour (Inside IR35) Job Description- 1. Develop measurement systems/capabilities, destructive tests, non-destructive tests for manufacturing processes. 2. Develop control plans consistent with product classification, potential defect types, defect frequency, severity, patient risk, process capability, process controls, etc. 3. Develop, interpret and implement appropriate process monitoring and control methods consistent with the level of process/product risk 4. Collect data and execute/conduct various analytical/statistical analysis and interpretations as part of process improvements and day-to-day support. 5. Develop, interpret and implement standard and non-standard sampling plans 6. Assess the effectiveness of measurement tools, destructive tests, non-destructive tests, measurement system analysis. 7. Accountability and ownership for sampling plans of all types including the acceptability of risk given the product classification, potential defect types, defect frequency, severity, patient risk, process capability, process controls, etc. including assessing, applying and interpreting acceptance sampling standards for manufacturing data. 8. Assess and interpret common versus special cause variation in manufacturing processing and determine the adequacy of current process limits 9. Technical training and experience using Statistics, Lean and Six Sigma Methodologies are required including Measurement System Analysis, SPC, DOEs, 10. A thorough understanding of GMP/ISO regulations and validation regulations is preferred. Reliability, etc.
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