Changing lives. Building Careers.
Joining us is a chance for you to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us, change equals opportunity. Every day, more than 4,000 of us are challenging what’s possible and making headway to help improve outcomes.
The Staff Manufacturing Engineer, Life Cycle Management (LCM) will work within the Integra Lifesciences CSS Engineering organization to support the manufacturing, launch readiness and production stability requirements of existing products. This position will provide technical expertise and project management in the areas of medical device DFM, supplier selection, supplier management, COGs management, process development and validation and production stability.
ESSENTIAL DUTIES AND RESPONSIBILITIES:
- Work in cross-functional Life Cycle Management project teams including R&D, Quality Assurance, Supplier Quality, Planning, Purchasing, Regulatory, and Manufacturing to develop and improve surgical products for the neurosurgical medical device industry.
- Recognized manufacturing process technical expert who can provide engineering knowledge and oversight to develop manufacturing processes and resolve manufacturing- and quality-related problems with existing products.
- Responsible for leading cross functional LCM projects, including developing and executing project plans, including stretch goals; controlling / adjusting project plans; developing alternate pathways or options; identifying and mitigating technical and project risks; presenting project status to management.
- Responsible for reviewing and updating applicable product specifications and drawings for legacy products. Responsible for identifying acceptance criteria for product specifications.
- Responsible for partnering with suppliers and internal manufacturing engineering teams to develop new processes and to review details of current manufacturing processes, review output of those processes, and make corrections where needed to improve robustness of output. Review may include activities such as process mapping, sampling, controlled design of experiments and component inspections.
- Provide leadership on critical supplier related programs, to ensure stable supply and to support the overall supplier relationship.
- Responsible for managing corrective actions and the implementation of all corrective actions to ensure improvements are attained.
- Responsible for designing and implementing control plans and monitoring processes at internal and external manufacturing sites to ensure processes are controlled and stable.
- Utilizes time management techniques (e.g., prioritization, goal setting, scheduling, etc.) to better balance workload; identifies ways to enhance the way work is done to save time and enhance efficiency.
- Proactively manages priorities based on changing needs; adjusts priorities to minimize impact to other business needs; communicates priorities as appropriate.
QUALIFICATIONS:
Education:
- Minimum of a bachelor’s degree in mechanical, Manufacturing, Materials or Biomedical Engineering or equivalent is required. Master’s degree preferred.
Experience:
- A minimum of 7-9 years applied experience with a B.S. and 5-7 years with a M.S. is required.
- Experience in the medical device industry is preferred.
- Minimum of 5 years of Project Management experience is required, PMP certified preferred.
- A keen insight of supply chain processes and ability to drive supply initiatives is required.
- A broad knowledge of manufacturing processes applicable to medical device manufacturing is required.
- Demonstration of an in-depth knowledge of relevant products & surgical techniques is preferred.
- Design experience and knowledge of the full product life cycle is required.
- Advanced knowledge in the application and selection of medical grade materials and the ability to match manufacturing processes with specific technologies is strongly preferred.
- Proficient knowledge of Process Excellence / Six Sigma statistical analysis techniques and its application in manufacturing processes is strongly preferred.
- Knowledge of GD&T standards is strongly preferred.
- Knowledge of how to execute GMPs, ISO 13485 Design Control, and manufacturing process IQ, OQ, PQ qualifications as related to medical devices is required.
- Strong technical communication skills and demonstrated ability to work independently with external suppliers is required.
- This position will require up to 15% travel.
Job Type: Full-time
Benefits:
- 401(k)
- 401(k) matching
- Dental insurance
- Health insurance
- Health savings account
- Paid time off
- Referral program
- Vision insurance
Experience level:
Schedule:
Work setting:
Work Location: One location
