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Sr. Mechanical Engineering Manager
Ommo is the pioneer of permanent magnet-based 3D tracking technology, providing ultra-precise 6DOF tracking for tiny sensors in real-time, at up to 1,000 times per second. We track the position and orientation of tiny sensors that are less than 1mm in size, with up to 0.1mm precision. Serving as a localized GPS for surgical navigation systems, our technology will eventually be used for a variety of digital transformation use cases, including virtual training, robotics, and human-machine interfaces.
We are seeking an experienced and driven Sr. Mechanical Engineering Manager to lead our mechanical product development team. In this role, you will lead a team of engineers and oversee the entire lifecycle of mechanical product design, from concept through mass production, ensuring high standards of quality, functionality, and manufacturability.
Roles & Responsibilities
Product Development Leadership
Oversee the entire mechanical product development lifecycle from concept through to mass production, ensuring high standards of quality and innovation.
Lead the design and prototyping of test fixtures and equipment for R&D and production, ensuring product reliability and manufacturability.
Technical Excellence
Create and review engineering drawings with a focus on GD&T best practices, ensuring compliance with standards and optimizing for manufacturing processes.
Perform engineering calculations (e.g., forces, stress, deflection, wear) and develop FEA models/simulations to validate designs.
3D CAD design for various manufacturing methods, including milling, turning, and injection molding.
Conduct and manage design reviews and releases in alignment with project schedules.
Team Management and Leadership
Lead, mentor, and manage a team of mechanical engineers, fostering technical growth and supporting project success.
Drive team performance by setting clear objectives, managing workloads, and providing regular feedback.
Cultivate a collaborative and innovative team culture, promoting continuous improvement and knowledge sharing.
Documentation and Compliance
Develop and manage product/project documentation throughout the product life cycle in line with the company’s ISO13485 Quality Management System (QMS).
Manage the creation and review of documentation such as Product Development Plans (PDP), Design Inputs/Outputs, and Verification & Validation Plans.
Oversee the creation and review of Failure Mode and Effects Analysis (FMEA), as well as Engineering Change Requests (ECRs).
Quality and Process Management
Analyze manufacturing data to ensure compliance with requirements and quality standards.
Plan and coordinate manufacturing process and material research and development activities.
Approve engineering documentation, drawings, and ECRs as required.
Qualifications
3-5 years of Senior Level Mechanical Engineering Experience; or related discipline
3-5 years of Engineering Management Experience
3+ years of relevant experience in medical device design/manufacturing or similar fields
Bachelor’s degree in Mechanical Engineering or related fields
Experience and skills in conflict resolution & people management.
Lead engineer or manager for product(s) that made it to series production
Proficiency in 3D CAD design, FEA, and 2D drafting/ drawings
Experience with medical device design & manufacturing documentation throughout the product development process
Experience with ISO13485 quality system
Self motivated and capable of driving and leading projects
Good planning and time management skills
Comfortable with and capable of solving very complex and ambiguous problems and managing multiple projects simultaneously
Nice to Have
Siemens NX Experience
CAM & CNC experience
Location
This position is an in-office role at our Headquarters in Carrollton, TX
Salary & Benefits
$120,000 - $140,000
PTO
Equity
Medical, Dental & Vision
401K & 401K Matching