| Requirement :: Quality Engineer :: Cleveland, Mississippi ::c2c at Cleveland, Mississippi, USA |
| Email: [email protected] |
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http://bit.ly/4ey8w48 https://jobs.nvoids.com/job_details.jsp?id=737089&uid= From: Navya gupta, Stellentit [email protected] Reply to: [email protected] Hello, I hope you are doing well! Kindly acknowledge me, are you Comfortable with this Position then please share me your updated resume . Job Title:- Quality Engineer Location:- Cleveland, Mississippi C2c Job Description Position Summary: The Quality Assurance Engineer provides technical support for various quality system processes to help ensure excellent product quality throughout product lifecycles. Position Responsibilities: Drive continuous improvement actions focused on product quality. Works with Engineering and Manufacturing to develop acceptance criteria for production processes. Works with Service and the Complaint Handling Unit to investigate product problems, perform root cause analysis and identify possible corrective actions. Analyzes production quality data to identify trends or issues which require action or CAPA activity. Assists in creating and implementing procedures in the quality management system. Assists in the review and disposition of nonconforming materials. Assists in the creation and validation of manufacturing processes. Conducts internal audits of production processes and report results. Reviews manufacturing process and part deviations. Creates quality alerts when acceptance activities need to be adjusted. Supports external regulator or customer audits Provides response to inquiries related to quality assurance arising from tenders or other sales efforts. Performs other duties as requested. Show Less Additional Skills & Qualifications Validation and risk and QFD and FDA and ISO and CFR and (ASQ or Rela) Essential competencies: Bachelor of Science degree in Engineering or related field. 3+ years relevant work experience. Demonstrated ability to analyze, evaluate and control risk following lifecycle risk management standards (e.g. ISO 14971). Experience with manufacturing / quality methodologies such as QFD, six-sigma, lean, etc. Understanding of statistical analysis techniques and tools. Experience with formal quality systems such as ISO 13485 or ISO 9001 and or CFR 210 & 211. ASQ or related quality certification is preferred. Work experience in a FDA regulated environment is preferred. Proficiency in reading and understanding technical product documentation (diagrams, schematics, flow-charts, etc.) Proficient in the use of Microsoft Office tools such as Word, Excel, PowerPoint, Outlook, etc. Comfortable with using PC tools and Windows OS, with a working knowledge of local and network based file systems. Excellent verbal and written communication skills using the English language. Able to coordinate multiple activities and actions of persons contributing to assigned tasks. Detail oriented with good organizational and record keeping skills. Ability to work independently and as part of a team. Proactive and timely in execution of assigned tasks. Able to be flexible and adaptable when needs and priorities change External Communities Job Description Essential competencies: Bachelor of Science degree in Engineering or related field. 3+ years relevant work experience. Demonstrated ability to analyze, evaluate and control risk following lifecycle risk management standards (e.g. ISO 14971). Experience with manufacturing / quality methodologies such as QFD, six-sigma, lean, etc. Understanding of statistical analysis techniques and tools. Experience with formal quality systems such as ISO 13485 or ISO 9001 and or CFR 210 & 211. ASQ or rela Navya Gupta Sr. IT Technical Recruiter Phone:- 3212189059 Email: [email protected] Gtalk: [email protected] Linkedin id:- linkedin.com/in/navya-gupta-1a879024a Keywords: information technology Idaho http://bit.ly/4ey8w48 https://jobs.nvoids.com/job_details.jsp?id=737089&uid= |
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| 02:24 AM 11-Oct-23 |