Instrument Engineer Salary in Boulder, CO

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 Quality Engineer IICareers that Change Lives A career at Medtronic is like no other. We're purposeful. We're committed. And we're driven by our Mission to alleviate pain, restore health and extend life for millions of people worldwide. LOCATION: This position will support the Advanced Surgical Instruments Manufacturing business 5 days onsite within Medtronic's Surgical Innovations group located in Boulder, CO. A Day in the Life This role is responsible for ensuring all aspects of the manufacturing process produce products to the highest possible reliability and quality. Some responsibilities include investigating and evaluating nonconforming devices and process identified during the manufacturing process as well as determining and implementing robust corrective actions to address the issues. Additionally, this role is responsible for identifying and validating improvements to reduce cycle time and improve overall production cell reliability. Monitoring and evaluation of complaints on devices used during surgical procedures is also required. Responsibilities may include the following and other duties may be assigned. 5 day on site support of daily manufacturing operations including troubleshooting of equipment, investigation of defects, and validation of equipment/processes. Develops, modifies, applies and maintains quality standards and protocol for processing materials into partially finished or finished materials product. Collaborates with engineering and manufacturing functions to ensure quality standards are in place. Devises and implements methods and procedures for inspecting, testing and evaluating the precision and accuracy of products and production equipment. Designs or specifies inspection and testing mechanisms and equipment; conducts quality assurance tests; and performs statistical analysis to assess the cost of and determine the responsibility for products or materials that do not meet required standards and specifications. Ensures that corrective measures meet acceptable reliability standards and that documentation is compliant with requirements. May specialize in the areas of design, incoming material, production control, product evaluation and reliability, inventory control and/or research and development as they apply to product or process quality. Qualifications - External Must Have: Minimum Requirements Bachelors degree required 2 years of quality experience required Nice to Have Experience working in a fast paced Manufacturing environment Medical Device experience Experience in quality engineering Physical Job RequirementsThe 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.Benefits & CompensationMedtronic offers a competitive Salary and flexible Benefits PackageA 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.Salary ranges for U.S (excl. PR) locations (USD):The base salary range is applicable across the United States, excluding Puerto Rico and specific locations in California. The offered rate complies with federal and local regulations and may vary based on factors such as experience, certification/education, market conditions, and location. Compensation and benefits information pertains solely to candidates hired within the United States (local market compensation and benefits will apply for others).Medtronic benefits and compensation plans About MedtronicWe 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 90,000+ 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 law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.At Medtronic, most positions are posted on our career site for 3-7 days.

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 LifeThe Senior Regulatory Affairs Specialist (Sr. RAS) is responsible for collaborating, planning and executing regulatory activities related to the Basic Energy and Access and Instrument product portfolio modifications. Activities include submissions ( e.g., 510(k), CE technical file), regulatory compliance assessments, compile international submissions and supporting EU MDR implementation. The Sr. RAS MDR role translates regulatory requirements into project/product requirements and collaborates cross-functionally, while ensuring timely and high-quality execution of assigned regulatory deliverables. This position is most suited for individuals with a broad background covering the total regulatory life cycle of medical devices and strong working knowledge and experience with reviewing advertising and promotional materials for medical devices. The initial project scope for this employee will be related to regulatory sustaining activities. NPD activities may be tied into the role later on.Location: Strong preference to have candidates work hybrid from Boulder, CO. Remote within the U.S. may be considered for the right candidate.Responsibilities may include the following and other duties may be assigned.Provide strategic input and technical guidance on regulatory requirements for new technologies and product modifications, considering both domestic and international regulationsPrepare 510(k) submissions and technical documents to support CE mark and other international submissionsParticipate in negotiations and interactions with regulatory authorities during the development and review processProvide business and product information to the international regulatory affairs team to enable development and strategies and requirements and communicate that information to the business teamSupport international product registrations as neededManage multiple projects and prioritize tasks on day by day basis to meet project schedulesInterface with engineering, quality, clinical, marketing, and other functions as needed to fulfill responsibilitiesReview promotional and advertising materialMaintain current regulatory knowledge of domestic and international regulations, guidelines, and standardsCreate or revise departmental procedures to improve operations or to reflect changing regulatory requirementsParticipate in internal and external audits as neededMaintain Regulatory affairs documentation to support compliance with applicable regulatory requirementsDirects or performs coordination and preparation of document packages for regulatory submissions from all areas of company, internal audits and inspections.Leads or compiles all materials required in submissions, license renewal and annual registrations.Keeps abreast of regulatory procedures and changes.May direct interaction with regulatory agencies on defined matters.Perform other duties as assigned or requiredRequired Knowledge and Experience: Bachelors degree with 4+ years of regulatory affairs experience in the medical device, biotech or pharmaceutical industryORAn advanced degree with 2+ years of regulatory affairs experience in the medical device, biotech or pharmaceutical industryNice to HaveKnowledge of FDA and EU MDR requirementsExperience of working with all classification of product in the U.S and/or EU.Design Dossier and/or Technical Documentation experienceTechnical WritingInternational medical device regulatory submission/approval experience, to include FDA and EU (specifically EU MDR)Product Labeling requirements and standardsMay have practical knowledge of project managementSystems Knowledge such as RA systems, Agile, SharePoint, or Quality Management SystemsPhysical Job RequirementsThe 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.Benefits & CompensationMedtronic offers a competitive Salary and flexible Benefits PackageA 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.Salary ranges for U.S (excl. PR) locations (USD):$88,800.00 - $133,200.00This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).The base salary range is applicable across the United States, excluding Puerto Rico and specific locations in California. The offered rate complies with federal and local regulations and may vary based on factors such as experience, certification/education, market conditions, and location. Compensation and benefits information pertains solely to candidates hired within the United States (local market compensation and benefits will apply for others).Medtronic benefits and compensation plans About MedtronicWe 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 90,000+ 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 law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.At Medtronic, most positions are posted on our career site for 3-7 days.

Who We Are: As a recognized leader in space science research and spacecraft instrumentation, avionics, and electronics, we work to reveal the secrets of our solar system and the universe. Objectives of this Role: This position will participate in the research and development of experimental, laser-based, spaceflight instrumentation enabling in-situ geochronology investigations across the Solar System.Work in multidisciplinary laboratory environment to design, build, and optimize novel spacecraft instrumentation for scientific missions to the moon and beyond.Contribute to the design, development, and hands-on fabrication, assembly, integration, and test of instrumentation systems from concept to flight instrument delivery.Support senior R&D personnel in cutting edge research involving pulsed lasers, mass spectrometry and high-speed data acquisition systems.Daily and Monthly Responsibilities: Work with scientific personnel to design, build, and test laser-based instrumentation capable of in-situ isotopic geochronology.Hands-on work with of Class IIIb/Class IV pulsed and CW lasers, ultra-high vacuum systems, pressurized gases, cryogens and high-voltage systems.Typical duties will involve the formulation and implementation of approaches to solving a wide array of experimental flight hardware problems - focused on the design, assembly and control of mechanical and electrical systems for data collection.Collaborate in the design, fabrication and performance validation of various optomechanical systems and interfacing with external vendors to procure instrumentation hardware, system sub-components and laboratory test equipment.Experimental data collection in an optical laboratory environment, LabView data acquisition and control system development, and CAD modeling of new hardware assemblies.Requirements: Requires a Bachelors or a Masters or a PhD in Aerospace Engineering, Systems Engineering, Electrical Engineering, Computer Engineering, Optical Engineering, Engineering Physics, Applied Physics or a related engineering field.1 year: Those with a PhD: experience with optomechanics, lasers, and high vacuum systems. Academic or professional experience working in a laboratory environment.1-3 years: Those with a BS or MS: experience with optomechanics, lasers, and high vacuum systems. Academic or professional experience working in a laboratory environment.1 year: Demonstrated experience in building experimental systems, scientific instruments or engineering test beds.A valid/clear driver's license is required. Special Requirements: Work assignment is in Boulder, Colorado. Must be a U.S. person (i.e., U.S. citizen, non-U.S. citizen national, lawful permanent resident, asylee, or refugee) due to ITAR work in section. Job Locations: Boulder, Colorado Salary Range: $64,459.00 - $131,061.00 For more information about this division, visit the Solar System Science & Exploration home page. For benefits information at our San Antonio location, click here. For benefits information at all other locations, click here. An Equal Employment Opportunity/Affirmative Action Employer Race/Color/Religion/Sex/Sexual Orientation/Gender Identity/National Origin/Disabled/Veteran Committed to Diversity in the Workplace