|
Systems Engineer, Manufacturing Engineering - Los Angeles California
Company: ResMed Inc Location: Los Angeles, California
Posted On: 01/29/2025
Systems Engineer, Manufacturing EngineeringPosition OverviewThe Systems Engineer, Manufacturing Engineering will play a key role in the implementation and optimization of systems and processes for the manufacturing of injection-molded CPAP masks. This is an exciting opportunity to work on challenging projects, collaborate with cross-functional teams, and gain exposure to advanced manufacturing techniques in a regulated, high-precision industry. Main responsibilities include implementation of manufacturing processes, equipment, facilities and documents, to meet the current and future production volume, quality, OHS and cost requirements. Key deliverables include conducting prototyping and verification activities to determine the feasibility/suitability of a design. Assists in the development, execution, and testing of new and existing products.You will work closely with experts in design, production, and quality assurance, ensuring that all processes meet industry standards while driving innovation and efficiency. This position is ideal for a recent graduate eager to apply their engineering knowledge and build a rewarding career in medical device manufacturing.Key Responsibilities - Process Design & Optimization:
- Work with Product Development to develop and maintain a complete, concise validated manufacturing system design that satisfies the product requirements with seamless integration of systems and subsystems.
- Implement continuous improvement initiatives using lean manufacturing and Six Sigma principles.
- Conduct process risk analysis to identify all reasonable risks and appropriate mitigations.
- Production Support:
- Analyze production data to identify trends, troubleshoot issues, and recommend corrective actions.
- Work with the operations team to resolve technical challenges, minimizing downtime and ensuring smooth production flow.
- Equipment & Tooling:
- Assist in the design, procurement, and validation of manufacturing equipment and injection molds.
- Conduct tooling trials and support the qualification of new tools for production.
- Validation & Compliance:
- Perform process validations (IQ, OQ, PQ) and maintain documentation to meet regulatory and quality requirements.
- Ensure all manufacturing processes comply with ISO 13485 and other applicable medical device standards.
- Collaboration & Communication:
- Collaborate with R&D, Quality, and Production teams to implement new product designs into manufacturing processes.
- Communicate technical concepts and progress effectively to both technical and non-technical stakeholders.
- Data Analysis & Reporting:
- Utilize data analysis tools to monitor key performance indicators (KPIs) and support decision-making.
- Prepare detailed reports and presentations on process performance and improvement initiatives.Qualifications
- Bachelor's degree in Systems Engineering, Mechanical Engineering, Manufacturing Engineering, or a related field.
- Strong foundational knowledge of injection molding processes, materials (e.g., thermoplastics, silicones), tooling and related automation (minimum 2-5 years of experience).
- Proficiency in CAD software (e.g., SolidWorks, AutoCAD) and familiarity with simulation tools (e.g., Moldflow) is preferred.
- Excellent problem-solving skills, with the ability to analyze and interpret complex data.
- Familiarity with regulatory requirements in medical device manufacturing is a plus (e.g., FDA, ISO 13485).Preferred Skills & Attributes
|
|