WHK Manufacturing Engineer

The TSE Family of Companies•Clearwater, FL

94d•Onsite

About The Position

Manage and improve all processes within the WHK medical device manufacturing department. Work with Quality to ensure all systems are in compliance with ISO 13485. Implement new processes and assist with onboarding of all new business. Set-up and manage all BOM’s and Routings in ERP system for new part introduction and for any process changes. Promote safety, housekeeping, and area improvement initiatives.

Requirements

College degree (BS) required in an Engineering discipline.
Minimum of 3-5 years manufacturing experience in an ISO 13485 regulated environment.
Experience working in a Clean Room environment.
Prior hands-on experience with injection molding and extrusion machinery required.
MS Office experience required – Outlook, Excel, and PowerPoint.
Ability to express thoughts clearly, both verbally and in written context.
Ability to write reports and business correspondence.
Ability to communicate effectively.
Strong knowledge in working with the MS Office Suite.
Understanding of all basic mathematical skills.
Understanding of trigonometry and angular relationships is necessary in order to understand and interpret blueprints.
Familiarity with the different processes required to process materials through a manufacturing environment.
Ability to use hands, fingers, and arms.
Ability to talk and/or hear.
Ability to lift and/or move up to 50 lbs.
Specific vision abilities required include close vision, depth perception, and ability to adjust focus.

Nice To Haves

Lean 6 Sigma training and certification highly desired.

Responsibilities

Work with Quality to ensure that all processes are in compliance with ISO 13485 requirements.
Write IQ/OQ/PQ validation protocols, execute validation protocols for new equipment and process changes, and write summary reports for management review and approval of all validations.
Lead, participate, and assist in root cause analysis of customer complaints and process waste issues with accountability for corrective action implementation.
Assist with developing machine specifications for new equipment and develop and modify equipment layout to generate process flow.
Identify potential equipment upgrades and/or new equipment requirements and complete cost analysis and justification for any capital request.
Guide Kaizen events and improvement efforts using Continuous Improvement tools and Lean 6 Sigma concepts.
Manage projects and multitask effectively, with attention to meeting deadlines and customer commitments.
Interact with customers concerning inquiries.
Take new products from inception to prototype and into production.
Work within a Clean Room environment and manage change in such an environment.
Create part drawings, tool drawings, and 3D models of new parts and assemblies.
Develop, monitor, and report key production KPI’s during daily production meetings.
Create work instructions, batch sheets, and process standard work for existing and new operations.
Assist with coordination of equipment calibration program as well as management of equipment Preventive and Predictive maintenance programs.
Revisit established production methods to seek out opportunities for improvement in safety, quality, and productivity.
Assist with special projects as needed.