Inspector I- 2nd Shift

We anticipate the application window for this opening will close on - 27 Apr 2026 At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world. A Day in the Life At Medtronic, we act boldly, compete to win, move with speed, foster belonging, and deliver results—the right way. This is the Medtronic Mindset, defining how we work and what we value. Our brand is rooted in action, and every team member plays a vital role in bringing our culture to life. We recognize your extraordinary potential to help ensure future generations live better, healthier lives. A career at Medtronic is purposeful, mission-driven, and unlike any other. We are committed to alleviating pain, restoring health, and extending life for millions worldwide. At Medtronic, we bring bold ideas forward with speed and decisiveness to put patients first in everything we do. In-person exchanges are invaluable to our work. We’re 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. Inspect and/or test parts, finished goods or re-worked items according to established specification and testing methods; provide training and work coaching as necessary. Document results; approve/reject items according to established standards. Assure record accuracy for traceability according to established practices. Responsible for maintaining training records including a review of the QA Inspector Training Matrix for accuracy and appropriateness at least annually. Monitor various manufacturing/ quality processes to assure component/product control, SOP and GMP control.  Initiate corrections/ improvements when necessary. Perform data collection; interpret and analyze information to provide recommendations for solution. Perform in process, pre-sterilization and post-sterilization testing; release conforming lots and document non-conforming lots. Work within multi-functional teams, QA or cellular production and demonstrate a service attitude throughout the organization. Initiate specification change orders for process and/ or quality related improvements. Records coordinator duties as required. Perform production related computer transactions. Required Knowledge and Experience: No prior experience required; comprehensive training will be provided. Ability to read and write in English in order to understand work instructions, safety protocols, and communicate effectively within the team. Nice to Have: Previous experience in material handling, warehouse, or inventory management Experience in a manufacturing or clean room environment 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 requireme ... (truncated, view full listing at source)