Job Location : Ormond Beach,FL, USA
Company Description
Command Medical products, LLC is entering a new chapter, building on almost 40 years of successful medical device contract manufacturing. We are looking for someone with the technical skills that fits our culture and core values.
We exist to enhance, sustain and save lives.
If like working hard with a great team, while having fun, CMP, LLC may be a good fit for you.
Role Description
This is a full-time on-site role for an Engineering Manager at Command Medical Products, LLC located in Ormond Beach, FL. The Engineering Manager will be responsible for team leadership, project management, and integration.
Lead & Develop - Oversee daily engineering operations, mentor your team, and build a high-performing culture.
Drive New Product Launches - Collaborate with customers and cross-functional teams to ensure products are designed for manufacturability (DFM) and assembly (DFA).
Optimize Processes - Lead process development, validation (IQ, OQ, PQ), and continuous improvement initiatives.
Risk Management - Apply FMEA and other tools to identify and mitigate manufacturing risks.
Continuous Improvement - Implement Lean Manufacturing principles to enhance efficiency, quality, and cost savings.
Standardization - Establish best practices, standardized workflows, and technical documentation.
Performance Metrics - Improve key KPIs, including cost reduction, cycle time, and product quality.
Collaborate Cross-Functionally - Work closely with Sales, Quality, Operations, and Supply Chain teams to ensure engineering goals align with company objectives.
Manage Budgets - Oversee departmental budgets and allocate resources efficiently.
Stakeholder Communication - Represent engineering in internal meetings, task force groups, and customer engagements.
Qualifications
Education: Bachelor's in Engineering (Mechanical, Biomedical, or related field). Master's preferred.
Experience: 7+ years in medical device manufacturing, with 3+ years in leadership.
Regulatory Knowledge: Strong understanding of ISO 13485, FDA 21 CFR Part 820, and process validation.
Technical Expertise: Hands-on experience with Lean Manufacturing, process validation, automation technologies, and capital/expense budgeting.
Industry Experience: Preferred background in extrusion, RF welding, and injection molding.
Software Proficiency: CAD tools (SolidWorks, AutoCAD), statistical analysis (Minitab), and project management tools (Microsoft Project preferred).
Leadership & Communication: Proven ability to build teams, manage projects, and effectively communicate technical concepts.
Project Management: Demonstrated experience in delivering results within tight deadlines and budgets.