Senior Supplier Quality Engineer Grand Rapids, MI
Job Location:
Grand Rapids, MI - USA
Yearly Salary:
Posted:
Application Deadline:
Vacancies:
Job Summary
Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain restore health and extend life. Our 95000 employees work across more than 150 countries to put patients first developing innovative medical technologies that improve the lives of 72 million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose growth and impact.
The Grand Rapids Michigan manufacturing site produces approximately 600 finished products including cannulae and beating heart products used across Medtronics cardiovascular portfolio. The Supplier Quality Engineering function partners closely with suppliers and cross-functional teams to ensure purchased materials components and finished devices meet quality regulatory and operational requirements throughout the product lifecycle.
This position is based in Grand Rapids MI and requires onsite work five (5) days per week to support supplier quality activities manufacturing operations and cross-functional collaboration. This role has minimal travel.
As a Senior Supplier Quality Engineer you will support supplier quality management activities for purchased materials and components used in manufacturing. This role is responsible for supplier performance oversight investigation of supplier-related quality issues implementation of supplier controls and support of product and process changes to ensure compliance with quality system and regulatory requirements.
Primary Responsibilities:
Manage supplier quality performance and monitor supplier compliance with quality requirements for materials components and services.
Lead investigations related to supplier quality issues nonconforming materials Supplier Corrective and Preventive Actions (CAPAs) Material Review Board activities and inspection findings.
Coordinate supplier onboarding activities including Approved Supplier List (ASL) additions and supplier setup across applicable quality and business systems.
Partner with engineering and cross-functional teams to develop product acceptance strategies supplier control plans and quality requirements for new products and processes.
Define receiving inspection requirements and support validation of internal test methods associated with supplied products.
Evaluate supplier change notifications and assess potential impacts to manufacturing operations inventory acceptance activities and product configurations.
Apply statistical quality techniques to analyze supplier performance identify trends and implement corrective actions.
Drive continuous improvement initiatives using Lean Six Sigma Kaizen and other quality improvement methodologies.
Required Qualifications:
Requires a Bachelors Degree in Engineering Science or technical field with 4 years of work experience in Engineering and/or Quality OR Advanced Degree in Engineering Science or technical field with 2 years of work experience in Engineering and/or Quality OR PhD with 0 years relevant experience.
Preferred Qualifications:
Experience investigating quality issues nonconforming products corrective actions or supplier-related quality concerns.
Knowledge of quality systems regulated manufacturing environments or supplier quality processes.
Ability to analyze data and apply problem-solving methodologies to support quality and process improvements.
Experience in supplier quality engineering within the medical device industry or another regulated manufacturing environment.
Working knowledge of Quality System Regulation (21 CFR Part 820) ISO 13485 statistical quality control methods and Six Sigma principles.
Experience with supplier controls process validation auditing failure investigations nonconforming product management and protocol or report development.
ASQ Certified Quality Auditor or ASQ Lead Auditor certification.
Proficiency with Microsoft Office applications including Word Excel PowerPoint and Project.
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.
Recruitment Fraud Alert
We are aware of phishing scams targeting job seekers. Please keep the following in mind:
Apply only through official Medtronic channels. All legitimate Medtronic recruiting communications come from approved Medtronic platforms and official @ email addresses.
Medtronic will never ask for payment or sensitive personal information (such as bank account or Social Security details) during early stages of the hiring process. Any such requests are not legitimate.
If you receive a suspicious message claiming to be from Medtronic do not respond click links or open attachments.
If you have any questions concerns regarding the authenticity of a communication alleged to have been made by or on behalf of Medtronic please contact us immediately at .
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
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:
Senior 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
