Project Engineer 100% ONSITE - Westlake Village CA (This role is not eligible for work visa sponsorship) Caldera Medical's Mission - To Improve the Quality of Life for Women! Message from the Hiring Manager : The Project Engineer will lead projects and provide technical expertise to ensure the ongoing reliability, compliance, and cost-effectiveness of our existing medical device products. This role is crucial for supporting products throughout their lifecycle by resolving manufacturing issues, implementing design changes, and leading continuous improvement initiatives. The engineer will collaborate with cross-functional teams, including manufacturing, quality, supply chain, and regulatory affairs, to address challenges and maintain product quality. Duties and Responsibilities : Project Leadership : Lead small to intermediate-sized sustaining engineering projects, including product and process improvements, cost reduction initiatives, and component obsolescence management. Manufacturing Support : Act as a primary R&D resource for manufacturing and production issues. Work closely with the manufacturing engineering team to troubleshoot and perform root cause analysis on product and process failures and implement effective corrective and preventive actions (CAPAs). Design and Process Changes : Coordinate and complete the following as needed for all sustaining engineering objectives : a. Project Schedule b. Quality and Regulatory documents c. Labeling and IFU changes d. Design Requirements - Trace Matrix e. Design Specifications - Trace Matrix f. Real Time Aging retention, testing g. V&V testing, documentation h. Testing protocols and reports i. Support Engineering Evaluation of returned product when needed. j. Competitive product evaluation including standard testing k. Support change Orders, technical review, implementation when needed Required Knowledge, Skills and Abilities : Education : Bachelor's degree in Biomedical Engineering, Mechanical Engineering, Electrical Engineering, or a related field. Experience : 4+years of experience in a regulated industry, with a strong emphasis on medical device product development or sustaining engineering. Experience with Class II or Class III medical devices is preferred. Experience in medical device component and material processing, design, and manufacturing. A comprehensive understanding of ISO, GMP and FDA regulations for the development. Other Requirements : 1. Strong analytical and problem-solving skills and comprehensive understanding of design control processes, risk management, and validation of processes / designs. 2. Proven project management skills. 3. Experience with lean manufacturing and continuous improvement methodologies 4. Effective verbal, presentation and written communication skills. 5. Proficient in Microsoft Office, and MS project. 6. Working experience in Solidworks. 7. Working knowledge of medical device development, sterilization requirements and techniques, and medical device regulations. 8. Additional responsibilities may be assigned as needed to support business objectives. Travel Required
Project Engineer • Thousand Oaks, CA, United States