A Day in the Life As a Lead Engineer of the MEIC, you will collaborate with the sustenance and engineering teams globally. You will enable Product Development, Medical Devices Design Controls, and Medical Device Regulation activities in close conjunction with the global teams.
Medtronic is a world leader in providing health care products that benefit individuals well-being. Our organization contributes directly to this mission. Our business is growing significantly as the market demands reliable medical devices which look and feel more like consumer devices. As a result, we need a Lead Engineer who will ensure we deliver the best on-time with high quality for our products. Be a part of the Medtronic Engineering and Innovation Center (MEIC) in Hyderabad by applying your skills to the growth, development, and sustaining efforts of Medical Devices products within the center. We value what makes you unique. Be a part of a company that thinks differently to solve problems, make progress, and deliver meaningful innovations.
Responsibilities may include the following and other duties may be assigned:
- Demonstrate strong expertise in Medical Device Regulations, including experience in gap assessments and remediation activities.
- Interact with cross-functional teams to achieve project objectives and contribute positively to the engineering community.
- Own & Lead Standards Assessment Process from start to finish and assess project deliverables and critical milestones, working in collaboration with multi-disciplinary functions.
- Drive the implementation of new standards across all product families, ensuring consistency and compliance.
- Provides problem solving/trouble shooting support to internal MEIC team and improve efficiency and reduce cost.
- Develop and implement automation solutions for manual processes using Python, VB, or other relevant tools.
- Work independently with minimal supervision, taking initiative to determine and develop effective solutions.
- Provide mentorship and guidance to junior team members; review their work and support their professional growth. May also lead projects or manage specific processes.
- Apply project management skills to plan, schedule, and monitor project activities efficiently.
- Possess comprehensive knowledge of product development and its cross-functional aspects.
- Support the Product Development Team by applying relevant medical device standards and regulations to new products under development.
Required knowledge and experience:
- Bachelor s or Master degree in Mechanical / Production / Bio Medical Engineering with 8 to 12 years of relevant experience.
- Strong knowledge of medical device regulations such as IEC 60601, ISO 22442, and FDA guidelines.
- Hands-on experience in automating manual processes using Python, VB, or similar tools.
- Excellent verbal communication skills for effective collaboration with global teams.
Medtronic offers a competitive Salary and flexible Benefits Package
This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).