Job Description
Careers that Change Lives A Day in the Life Responsibilities may include the following and other duties may be assigned.
- Provides technical and sustaining engineering support in a manufacturing area.
- Recommends and implements equipment and process modifications to meet quality standards and improve production efficiencies, manufacturing techniques as well as production yields for existing products.
- Integrates equipment and material capabilities to meet process module target specifications and technology target specifications.
- Reviews product development requirements for compatibility with processing methods to determine costs and schedules.
- Interacts with product design and development personnel to ensure that processes and designs are compatible.
- May develop and conduct statistical analysis or recommend additions to document work.
- Leads the innovation, development and/or optimization of new manufacturing concepts, processes and procedures for transfer to manufacturing operations.
- This can include scouting and feasibility work, material selection, process and equipment selection, tooling / fixture and equipment installation and assessment of inputs, outputs and alignment to requirements.
- Develops manufacturing processes that are applicable to statistical process control and may develop those techniques including the measurement systems.
- Ensures processes and procedures are in compliance with regulations.
Must Have: Minimum Requirements - Bachelors degree required
- Minimum of 4 years of relevant experience, or advanced degree with a minimum of 2 years relevant experience
Nice to Have Nice to Have
- B.S. in Mechanical Engineering
- Experience in a Medical device manufacturing environment and regulated Industries.
- Experience on change control management processes.
Core technical requirements:
- Hands-on experience developing tools prototype (in term of form, materials and functions) until get them implemented as part of process improvement projects/ activities.
- Specific expertise by using programs/Software such as: SolidWorks, AutoCAD, ProE.
Additional requirements:
- Knowledgeable on the process for factory acceptance tests (FAT) and site acceptance tests (SAT) activities; including User and Design Requirements Documents.
- Knowledgeable on the process to write and execute validation protocols and reports:
- Equipment IQ
- Computer System Validations
- Process Characterizations
- Process OQ/PQ
- Methods Validations
- Knowledgeable on the process to draft and implement Calibration and Preventive Maintenance (PM) procedures; including critical spare parts identifications.
About Medtronic
Together, we can change healthcare worldwide. At Medtronic, we push the limits of what technology, therapies and services can do to help alleviate pain, restore health and extend life. We challenge ourselves and each other to make tomorrow better than yesterday. It is what makes this an exciting and rewarding place to be.
We want to accelerate and advance our ability to create meaningful innovations - but we will only succeed with the right people on our team. Let’s work together to address universal healthcare needs and improve patients’ lives. Help us shape the future.
Physical Job Requirements
The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions and Physical requirements that may be specific to each role. (ADA-United States of America) Additional Information
- Posting Date: Feb 28, 2022
- Travel: Yes, < 25 % of the Time