| Requirements for :: Manufacturing Engineer with Creo Experience :: Medical Device Domain at North Haven, Connecticut, USA |
| Email: [email protected] |
| From: Nirbhay singh, Appian infotech Inc [email protected] Reply to: [email protected] Hi, We Have Urgent requirements for Manufacturing Engineer with Creo Experience If you are interested in this position please share an updated profile on nirbhay.s @appianinfotech.com , or call on 276-910-0146 Ext 128. Role: Manufacturing Engineer Location: North Haven, CT (Onsite) Job Type: Long term project JOB Description: ESSENTIAL FUNCTIONS: Participate in Design for Assembly (DFA) / Design for Manufacturing (DFM) activities to verify manufacturability of Product Designs. Actively participate in PFMEA, DFMEA, Process Mapping, and Critical to Quality (CTQ) reviews assuring specifications are well defined and documented. Create and review process flow charts, assembly tooling strategies, assembly line layouts, balance tables, assembly capacity analysis, and EHS project plans. Participate in the development of capital expense requests, project schedules, make-buy analysis and other financial documents. Provide input for all assembly tooling required to support new product development activity Create, assemble, detail and review tooling and fixturing utilizing Creo and Solidworks software. Develop and review defining documents , RFQ packages, interact with suppliers during the quoting process, ensure supplier adherence to tooling specifications, oversee manufacture and qualification of assembly tooling. Develop Protocols and execute Factory Acceptance Testing (FAT) on all purchased tooling, systems and fixtures. Manage and support line validation / qualification activities for including IQ, OQ , MSA and PQ. Write testing protocols for product evaluations; oversee and analyze product evaluation requests. Create process documentation including SWI, Control Plans and job safety analysis sheets. Actively participate in Lean initiatives to stabilize production lines and reduce the time to transfer to Plant. DEPARTMENT SPECIFIC / NON-ESSENTIAL FUNCTIONS: Travel to supplier sites as required. International travel required. Mentor and guide less experienced employees for professional development and advancement. Continue to enhance engineering and leadership skills through additional training, development projects, and education. Follow established guidelines and management direction with regard to engineering decisions and departmental / company policy. Minimum Experience 3 Years Applicable Experience for mid-Level 7 years Applicable Experience for Senior level Skills / Qualifications Experience in CREO to review custom tooling, fixtures, gages, and components Review modification and development of Machine Specifications for manual, semi-automated and fully automated machines Basic understanding of Industrial Engineering principles including balance tables, process flow diagrams, line lay-outs, ergonomic designs, etc. Experience in assembly equipment technologies Experience with equipment and line process validations (IQ / OQ / PQ / MSAs) Working knowledge of Lean Principles and/or 6 Sigma Methodology Working knowledge of GD&T Working knowledge of FMEA Working knowledge of DFA and DFM principles Familiarity with statistical analysis including capability, process control, DOEs, control charts, etc. Minitab experience preferred, but not mandatory Experience or working knowledge of control systems, PLC logic, and vision systems Competencies Exemplify team-work approach Dynamic, positive attitude Strong interpersonal, communication, project management and presentation skills Strong design, trouble-shooting, assembly tooling, and manufacturing process skills Strong computer skills (Microsoft Office, Project, Mini-Tab) Ability to mentor and provide guidance to associate team members Ability to work with fellow employees and suppliers on an international level. Questions to be asked to candidate :- 1. If I worked with Automated equipment Assembly Equipment In Manufacturing 2. If aware of the Vision System 3. If have Experience with equipment and line process validations (IQ / OQ / PQ / MSAs) 4. Have you Participated in Design for Assembly (DFA) / Design for Manufacturing (DFM) 5. I have experience in statistical analysis including capability, process control, DOEs, control charts, etc. Minitab experience 6. If I have experience of Create and review process flow charts, assembly tooling strategies, assembly line layouts, balance tables, assembly capacity analysis, and EHS project plans 7. If having experience of PFMEA, DFMEA, Process Mapping, and Critical to Quality (CTQ) reviews 8. Do you have experience of creating process flow charts, assembly tooling strategies, assembly line layouts, balance tables, assembly capacity analysis, and EHS project plans -- Regards Nirbhay Singh Appian Infotech Inc Contact No- 276 910 0146 Ext. 128 Email- nirbhay.s @appianinfotech.com LinkedIn:- https://www.linkedin.com/in/n-k-singh-430076245/ Keywords: Connecticut Requirements for :: Manufacturing Engineer with Creo Experience :: Medical Device Domain [email protected] |
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| Tue Apr 02 02:21:00 UTC 2024 |