Senior Incoming Inspection Supervisor
Boulder, CO - USA
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.
Senior Incoming Inspection Supervisor is a key Quality Assurance leader responsible for leading the Boulder Incoming Inspection team and driving risk-based prioritization across the QA organization. This role provides strategic and operational leadership for incoming inspection activities ensuring effective risk burndown regulatory compliance and alignment with business and quality objectives.
Responsibilities may include the following and other duties may be assigned.
Leads team in predetermined methods operations setups and prescribed specifications to inspect visually in-process and completed products such as electronic units and subsystems precision electromechanical assemblies or mechanical units subassemblies structural flaws internal defects and missing welds.
Uses various measuring devices and testing equipment.
Accepts rejects or reworks defective or malfunctioning units or systems.
Works from blueprints diagrams dial indicators preset micrometers scales fixtures customer specifications drawing or inspection instructions and checklists.
May monitor and verify quality in accordance with statistical process or other control procedures.
Performs line clearances after each lot to ensure all materials from the previous lot have been removed.
Assures smooth operating of the inspection unit maintaining daily records and reports.
Prioritizes schedules based on product introduction and manufacturing schedules maintaining a minimum turnaround time.
Makes recommendations for capital expenditures and manpower for inspection area.
Selects develops and evaluates personnel to ensure the efficient operation of the function.
Recommends new or enhanced methods procedures and standards.
Drives risk burndown activities by identifying quality risks recurring defects inspection escapes and process gaps and implementing actions to reduce risk to product quality compliance and supply continuity.
Leads and supports Quality Management System improvements related to inspection procedures documentation training effectiveness compliance and standard work.
Leads efficiency projects focused on improving inspection throughput reducing turnaround time eliminating non-value-added activities and optimizing use of people equipment and resources.
Maintains audit readiness for the inspection area by ensuring procedures records training and practices are compliant and inspection-ready for internal external customer and regulatory audits.
Supports audit activities and inspection responses including preparation participation gap identification and timely closure of actions.
Oversees MRB activities and NCMR product management to ensure nonconforming product is properly identified segregated reviewed dispositioned and closed in compliance with applicable procedures and quality requirements.
Partners cross-functionally with Manufacturing Quality Engineering Supply Chain and Operations to drive timely disposition of nonconforming material and reduce repeat issues.
Monitors trends in defects MRB NCMR rework and inspection performance to drive continuous improvement and sustainable corrective actions.
Supports CAPA NCR and broader quality improvement efforts through data analysis problem solving and implementation of corrective and preventive actions.
Required Knowledge and Experience:Understands basic management approaches such as work scheduling prioritizing coaching and process execution.
Requires advanced knowledge of job area typically obtained through advanced education combined with experience.
Requires 3 years of experience with a high school diploma or equivalent.
Preferred Skills (Nice to Have):
Experience in a regulated medical device or FDA / ISO 13485 manufacturing environment.
Working knowledge of MRB NCMR CAPA and nonconforming product disposition processes.
Experience supporting internal external customer or regulatory audits and driving audit readiness activities.
Lean Sigma continuous improvement or process optimization experience with demonstrated efficiency gains.
Experience with electronic quality systems and data-driven decision making using quality or inspection metrics.
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:
Manager
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