CX - Senior Manufacturing Engineer Job at Coghlin Companies Inc in West Boylston

Responsibilities:Under the direction of the Manager of Engineering, the Senior Manufacturing Engineer will:Provide engineering, operational, Lean manufacturing, Six Sigma leadership and mentoring.Lead by example and promote the criticality of strict compliance adherence at Cogmedix.Lead in the training of personnel, including customers and suppliers on workmanship and quality standards.Compliantly implement and maintain Cogmedix procedures. Collaborate with Program Managers, Manufacturing Engineers and other departments to analyze customer ECO's and ensure effective implementation to the production floor through proper use of the Cogmedix ECO process.As part of the ECO Process and new proposal review, oversee the management of the customer BOM structure, creation of part numbers and structuring of Supplier Relationships and costs.Define PP/PA/Phantom, Commodity codes, documentation packages commodity and Work Instruction evaluation.As part of the ECO Process, oversee the generation and updating of DMR Indexes to ensure accuracy.As part of the ECO Process, provide ECO final approval for release.Oversee ECO implementation performance metrics.Effectively interact with customers and internal departments to create value-add propositions.Working with all internal groups, identify trends and process gaps and suggest and assist in the implementation of corrective actions and process improvements.Collaborate with internal groups and customers to help determine root cause of customer issues, Complaints, and CAPAs. Oversee and ensure prompt ME responses to manufacturing floor quality issues, taking appropriate action within the Cogmedix Quality System and continually building strong rapport with customers and suppliers.Oversee the development and approvals of optimal work order routings and Device History Records.Review redlined documentation and review prior to sign off.Lead and oversee complex troubleshooting efforts. Lead Manufacturing Engineers in the generation of Rework Instructions and review and approve prior to implementation. Generate the more complex Rework Instructions and assist when needed. Lead and oversee the development and deployment of Lean Manufacturing Cells.Working with the Quality Department, support the review of quality and inspection plans.Oversee regular audits of calibrated tools, tools requiring Preventive Maintenance and perishable floor stock items.Oversee the training of Assembly Technicians, Test Technicians on procedures as needed. ME oversight, management and scope of work for Scaled Product Launch/transitions. Oversee and review the generation of process validation/qualification documentation (e.g., validation protocols, IQ/OQ/PQ) and lead the implementation of protocols and completion of reports.Lead and oversee the preparation of Process Flows, PFMEA's, Time Studies and Value Stream Mapping.Evaluate Product Performance Data and Internal Metrics for stability and continuous improvements, utilizing Six Sigma practices where appropriate, including SPC (statistical process control).Generate Manufacturing Engineering Bulletins to communicate Continuous Improvement Opportunities to customers.Contribute in DFcx exercises.Oversee and approve Risk analysis, Risk management and Risk reports.Oversee Customer Specific Daily Team Meetings.Oversee new customer documentation package review.Lead and oversee co-build activities.Assist in the containment of nonconforming product.Approve rework instructions and non-conformances.Review and approve Equipment enrollment forms.Train Manufacturing Engineers and Engineering Document Control Specialists.Support DFcx Engineering programs. Perform other activities as directed.Essential Requirements:Positive attitude, self-motivator, and tenacious follow up required.Superior customer service attitude.Excellent teamwork, communication, interpersonal and leadership skills.Exceptional attention to detail.Strong electro-mechanical and opto-mechanical orientation.Experience in ISO 13485 certified and cGMP organizations preferred.Proven problem solver with multitasking skills and the ability to prioritize tasks to align with the goals of the department and organization as a whole.Knowledge of IPC 610 and 620 standards beneficial.Advanced ability to read, interpret and understand engineering documentation including assembly drawings, detailed component drawings, optical schematics, electrical schematics, pneumatic schematics, and wire run lists.Must be able to climb stairs and lift up to 30 lbs.Bachelor's degree in science, engineering, or manufacturing discipline.Eight or more years of related manufacturing experience and technical document control may be considered in lieu of certain educational requirements.10+ year's professional experience in medical subassembly and finished device manufacturing preferred.Advanced Level Skills in MS Word, Excel and PowerPoint such as keyboard short cuts, creating forms, table techniques, working with images, text, and pivot tables preferred.Advanced Level Skills in MS Visio such as creating Visio diagrams, creating custom styles and templates, cross functional flow charts, linking drawings to other MS applications, working with data, custom reports, and exporting is valuable.SolidWorks and PDM experience is preferred.Advanced working knowledge of Lean concepts and Six Sigma Black Belt training is preferred.Note:The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification.They are not intended to be construed as an exhaustive list of all responsibilities, duties and/or skills required of all personnel so classified.Cogmedix is an Equal Opportunity Employer. Cogmedix does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, non-disqualifying physical or mental disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need.