Manufacturing Engineer I Warsaw, IN
Warsaw, IN - USA
Job Summary
At Medtronic you can begin a life-long career of exploration and innovation while helping champion healthcare access and equity for all. Youll lead with purpose breaking down barriers to innovation in a more connected compassionate world.
A Day in the Life
The Manufacturing Engineer I will be based at Medtronics Warsaw Indiana site part of a long standing manufacturing hub often referred to as the Orthopedic Capital of the World. The Warsaw campus is a cornerstone of Medtronics orthopedic and cranial/spinal technologies manufacturing producing highly regulated life changing medical devices in a fast paced production this role you will partner closely with production quality and operations teams to support daily manufacturing activities drive process improvements and ensure products are manufactured safely efficiently and in compliance with Medtronic and regulatory standards.This is an excellent opportunity for an early career engineer to build a strong foundation in medical device manufacturing within a collaborative engineering driven site. The Manufacturing Engineer I will be supported by experienced engineers and leaders gaining hands on exposure to continuous improvement process optimization and cross functional problem solving. Your work will directly contribute to products that alleviate pain restore health and improve patient outcomes around the world.
At Medtronic we bring bold ideas forward with speed and decisiveness to put patients first in everything we -person exchanges are invaluable to our work. Were working a minimum of 5 days a week onsite as part of our commitment to fostering a culture of professional growth and cross-functional collaboration as we work together to engineer the extraordinary.
Responsibilities may include the following and other duties may be assigned.
- Provides on-going shop floor support for all machining metal finishing and assembly methods for assigned product lines.
- Partner with Project Engineer and determine Make vs. Buy decisions.
- Participate in print review partner with Quality Engineering on determining gages and measurement procedures.
- May determine appropriate machine platform for product and review any necessary capital equipment requirements.
- Creates conceptual designs for fixtures gages and special cutting tools. May conduct tool design reviews with Tooling Team personnel purchasing personnel and outside tool suppliers. May determine outsourcing decisions as appropriate.
- Completes activities of the change control policy and Corrective and Preventive Action (CAPA) system in accordance with Medtronic Corporate CAPA system.
- Completes activities of Lean Sigma projects and process improvements.
- May represent Warsaw on new product launch activities and transfer of product.
- Initiates drawing changes with the product design engineer to improve manufacturing quality and reduce costs.
- May provide tooling selection input in partnership with the CNC Programmer to ensure existing tool maps. Troubleshoots CNC programming problems on the production floor. Coordinates necessary program changes with the appropriate CNC Programmer.
- Provides technical support to purchasing personnel and suppliers by interpreting product drawings initiating the development of manufacturing drawings and resolving technical production problems.
- Proactively execute and support development of validation/qualifications studies. Determine strategy with appropriate teams and ensure that groups are involved early on in the needs of the engineering group.
- Responsible for the investigation of change requests received in the Manufacturing Engineering department their rejection or approval development and implementation of any process changes and proper documentation of any such changes.
- Working with the appropriate groups; maintains manufacturing process sheets for all machining assembly and finishing operations.
- Makes appropriate changes in manufacturing methods processes and Manufacturing Process Planning documentation when dictated by engineering drawing changes. Documents all changes through the appropriate change control system.
- Resolves technical production problems on assigned product lines in machining metal finishing and assembly operations working with shop employees and quality personnel.
- Coordinates entry of all master data for assigned product lines. This may include Purchase Requests Capital Appropriation Request Inventory Approval Forms Material Masters Bills of Material routings production versions work centers and document information records.
- Coordinates update of production order data as needed
- Initiates improvements in current manufacturing methods and processes to improve part quality schedule performance and to reduce manufacturing costs.
- Trains shop employees on improvements to manufacturing methods products and new production equipment.
- Travel as required for company business transactions.
- May partner with Quality in risk management activities (i.e.: PFMEA)
- Provide periodic updates of assigned projects to senior management maintain project documentation project plans action item registers and actively manage risks related to cost quality and schedule.
- Performs other duties as assigned.
Minimum Requirements
- Requires a Bachelors degreewith 0 years relevant experience.
Nice To Have
- Basic working knowledge of applicable industry standards and regulatory requirements (e.g. ISO 13485 ISO 14971 MDD 93/42/EEC PAL CMDR and 21 CFR Part 820) and an understanding of how compliance impacts daytoday manufacturing and engineering activities
- Awareness of quality and regulatory expectations within a medical device manufacturing environment including when and how to leverage available resources to assess compliance impact and ensure adherence to established procedures
- Strong communication skills both oral and written
- Good interpersonal skills
- Ability to work in a fast paced environment
- Ability to work well under pressure and maintain positive enthusiastic attitude
- Eagerness to learn and expand responsibilities
- Ability to work effectively in a team environment and build strong working relationships.
- Willingness to participate in continuous improvement activities
For Baccalaureate degrees earned outside of the United States a degree that satisfies the requirements of 8 C.F.R. 214.2(h)(4)(iii)(A) is required.
Physical Job Requirements
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position but they are not an exhaustive list of all the required responsibilities and skills of this position.
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.
U.S. Work Authorization & Sponsorship
At Medtronic we are committed to fostering an environment where employees can thrive and make a meaningful alignment with our enterprise-wide workforce planning approach U.S. work authorization sponsorship (H-1B TN J etc.) is offered exclusively for Principal-level roles and above where specialized expertise aligns with long-term business needs. Roles below the Principal level require candidates to possess unrestricted U.S. work authorization at the time of hire and for the duration of employment.
Join us in our mission to alleviate pain restore health and extend lifewhere your unique background and perspective are valued.
Benefits & Compensation
Medtronic offers a competitive Salary and flexible Benefits Package
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits resources and competitive compensation plans designed to support you at every career and life stage.
The following benefits and additional compensation are available to those regular employees who work 20 hours per week: Health Dental and vision insuranceHealth Savings AccountHealthcare Flexible Spending AccountLife insurance Long-term disability leaveDependent daycare spending accountTuition assistance/reimbursement andSimple Steps (global well-being program).
The following benefits and additional compensation are available to all regular employees:Incentive plans 401(k) plan plus employer contribution and matchShort-term disabilityPaid time offPaid holidaysEmployee Stock Purchase PlanEmployee Assistance ProgramNon-qualified Retirement Plan Supplement (subject to IRS earning minimums) andCapital Accumulation Plan (available to Vice Presidents and above or subject to IRS earning minimums).
Regular employees are those who are not temporary such as interns. Temporary employees are eligible for paid sick time as required under applicable state law and the Employee Stock Purchase Plan. Please note some of the above benefits may not apply to workers in Puerto Rico.
Further details are available at the link below:
Medtronic benefits and compensation plans
About Medtronic
We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.
Our Mission to alleviate pain restore health and extend life unites a global team of 95000 passionate people.
We are engineers at heart putting ambitious ideas to work to generate real solutions for real people. From the R&D lab to the factory floor to the conference room every one of us experiments creates builds improves and solves. We have the talent diverse perspectives and guts to engineer the extraordinary.
Learn more about our business mission and our commitment to diversity here.
It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age color national origin citizenship status physical or mental disability race religion creed gender sex sexual orientation gender identity and/or expression genetic information marital status status with regard to public assistance veteran status or any other characteristic protected by federal state or local addition Medtronic will provide reasonable accommodations for qualified individuals with disabilities.
If you are applying to perform work for Medtronic Inc. (Medtronic) in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County you can findhere a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. Medtronic will consider for employment qualified job applicants with arrest or conviction records in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.
Required Experience:
IC
About Company
About Medtronic Together, we can change healthcare worldwide. At Medtronic, we push the limits of what technology 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 excit ... View more