Senior Manufacturing Engineer
Medivators
(Conroe, Texas)Medivators, a wholly owned subsidiary of Cantel Medical Corp. (NYSE:CMN), is a leading provider of infection control products and services that ensure the safe and proper disinfection of endoscopes and other devices.
The primary responsibilities include; leading and developing our current and future manufacturing processes by coordinating the engineering activities in support of the organizations manufacturing engineering needs.
- Provide senior-level technical support, training and guidance for all assigned engineering projects
- Support and provide expert guidance and training for fellow engineers and peers
- Provide technical support to all manufacturing departments and assigned new-product development projects
- Write, and or, update work instructions/part specifications, validation protocols, test reports, routine engineering reports, proof read and update technical documents (ECOs, MPs, QCs, rework instruction and cost)
- Interface with Internal and external resources in the review of the design changes and product line enhancements
- Engineering Project Management: develop/plan, manage and lead assigned engineering projects (cost savings/Six Sigma improvement projects)
- Perform detailed engineering assessments including, Process Capability (CPK), line layouts and line rebalancing initiatives, flow optimization and automation projects
- Support the organization growth initiatives and actively participate in the new product line introductions
- Actively participate in the organizations Operational Excellence program and provide the training and guidance required to support our associate’s growth in the understanding and application of Lean improvement process
- Analyze and review current requirements, workflow, design layout of equipment, and workspace for maximum efficiency
- Share in the coordination of the development and control of the company capital expense budgets
- Bachelor of Science in Electrical and/or Mechanical Engineering, Master’s degree is preferred
- A minimum of 5 years medical device manufacturing required (class II/III) and a minimum of 8 of engineering experience
- Strong understanding of Six Sigma and Process Excellence tools/methodologies
- Knowledge of electronic equipment troubleshooting and PCBA design
- Production equipment troubleshooting/adjustment knowledge (Ultrasonic welding, packaging-Tyvek/paper, Injection molding)
- Solid Process Validation Experience (IQ/OQ & PQs)
- Demonstrated organizational skills, ability to handle and prioritize multiple projects simultaneously
- Strong interpersonal skills, with the ability to relate and work in a fast paced manufacturing work environment
- Assembly Fixture Design Experience and PLC Programming
- Advanced Engineering Project Management Experience
- Capital Budgeting Experience
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