| Opportunity for Quality Engineer role - Need Medical devices experience at North Haven, Connecticut, USA |
| Email: [email protected] |
| From: Nora West, W3Global [email protected] Reply to: [email protected] Hello, Greetings from W3Global Inc!! I am not sure if you are looking for a new opportunity, but when I came across your resume, I felt that you might be the right fit for this new opportunity. Here is the job description. Job Title : Quality Engineer Employment Type : Contract, C2C, Full time / Direct Hire, 1099 Location : North Haven, CT, US Job Description Contribute to continuous improvements in overall product cost and quality. Participate in DFM / DFA activities assuring that packaging/production processes and equipment are taken into consideration. Collaborate with Quality Engineering to provide manufacturing support. Create standardized work and process maps that result in an optimized production system and extended value stream. Support line validation/qualification activities including IQ, OQ, MSA, and PQ. Perform root Cause Analysis (RCA), NCR, and CAPA responses. Need to conduct qualification, verification, and validation activities to produce medical devices. Work with CFT teams in troubleshooting problems on the production floor. Design, develop, test, and validate equipment and processes; analyze and interpret process models and recommend process improvements. Drive the execution of various validation and PFMEA activities as per the project plan Application of statistical and analytical methods such as SPC, SQC, and DOE. Contributor to the Capital Expense Request (CER) process, specify the cost for Packaging/Labeling/ sealing equipment with consideration to product standard cost targets and capacity demands. Provide detailed engineering analysis and documentation in the management of material disposition, process updates, NCR's and CAPA. Execute Site acceptance test and Factory acceptance test based on North Haven Execute Validation Gap analysis of various product families based in Medtronic Plan and initiate CDPs associated with the various validation activities Co-ordination with stakeholders Provide detailed engineering analysis and documentation in the management of material disposition, process updates, NCR's and CAPA. Qualification: BS Degree in Packaging Science, Mechanical Engineering, or Equivalent/MS Engineering Min 3 yrs. Applicable Experience in packaging engineering, medical devices, pharmaceutical, or related industry preferred. Broad knowledge of Mechanical/Manufacturing Engineering. Please let me know your interest and let's keep in touch until we make this happen Referrals appreciated and welcomed. Keywords: access management microsoft Colorado Connecticut Opportunity for Quality Engineer role - Need Medical devices experience [email protected] |
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| Sat Apr 13 01:46:00 UTC 2024 |