Production Worker Salary in Boulder, CO

Careers that Change LivesThe role of Product Consultant for the next-gen monitor and analytics is a crucial position within the Acute Care Monitoring business. Reporting to the Director of Marketing for the HealthCast portfolio, this role carries the responsibility of identifying customer needs and aligning them with broader business objectives.You will play a key role in defining the success criteria for the product and inspiring a team to transform that vision into a reality. Your primary focus will involve developing and effectively communicating the roadmap to both internal and external stakeholders. Collaborating closely with the engineering team, you will jointly create a world-class solution.Specifically, this position will oversee the HealthCast Hub Monitor roadmap, value proposition, and business cases, with a strong emphasis on analytics. Successful execution will require cross-functional collaboration with the software-focused product manager, identifying strategic partnerships, and making independent prioritization decisions while keeping patient and customer outcomes at the forefront.To excel in this role, strong business acumen is essential, along with the ability to work across teams to execute the roadmap, effectively communicate at all levels of the organization, prioritize development efforts, exert influence without formal authority, and successfully chart a direction for the organization Acute Care Monitoring is part of the Surgical Portfolio.This position is based in Boulder, CO and is open to remote within the United States, for well qualified candidates.A Day in the LifeProduct Management: Develop, align, and implement a product vision, strategy, and roadmap across HealthCast' businesses and global regions. Align with your portfolio leader and senior leadership on product priorities. Effectively and efficiently deliver results by working with various product groups (COTs), strategy team, hardware and software development teams. Drive global demand forecasting while partnering with operations to maximize supply and marketing teams to increase utilization. Determine customer needs, assess potential solutions, develop business case for investments and plan initial marketing messages. Translate data and analytics into product roadmap strategies and track the performance of the product and make informed decisions about future product development. Own competitive intelligence for your products, understand near and long-term implications for your product, and develop product strategies and tactics to defend against or overcome competitive actions. Manage technical debt reducing existing debt, considering implications of new features and requests. Continuous technical scanning to anticipate and plan for developments and technological changes across global regions. Drive launch planning for upcoming releases. Capture voice of customer and translate to features and enhancements for the platforms as well as prioritization decisions. Travel approximately 40% Must Have: Minimum Requirements Bachelors degree required 10+ years' experience in a product marketing/management, technical, clinical, or commercial role in a regulated industry is required, 8 years with and Advanced degree Nice to Have MBA or other Master's Product management experience in a regulated industry Experience in working with global teams from different cultures Experience in patient monitors in hospitals and analytics Experience in understanding and creating improved and new clinical workflows and analytics to enable the delivery of improved patient care Acute understanding of patient monitoring and workflow in hospitals, especially in OR, ICU, PACU, and stepdown Acute understanding of the hospital IT environment and how patient monitor data integrates with EMR systems Previous experience driving voice of stakeholder activities, product definition, program scope Experienced in business and financial modeling About MedtronicTogether, we can change healthcare worldwide. At Medtronic, we push the limits of what technology, therapies and services 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 exciting and rewarding place to be.We want to accelerate and advance our ability to create meaningful innovations - but we will only succeed with the right people on our team. Let's work together to address universal healthcare needs and improve patients' lives. Help us shape the future.Physical Job RequirementsThe 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, recruiter or local HR to understand the Work Conditions and Physical requirements that may be specific to each role. (ADA-United States of America)Medtronic Benefits and CompensationA 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. Learn more about our benefits here .This position is eligible for a short-term incentive plan. Learn more about Annual Salary and Medtronic Incentive Plan (MIP) on Page 6 here .The provided base salary range is used nationally in the United States (except in Puerto Rico and certain CA locations).The rate offered is compliant with federal/local regulations and may vary by location.

Clinical Lab Clinical Research Specialist (Clinical Research)In this exciting role as a Clinical Research Specialist, you will have primary responsibility to manage day-to-day operations of clinical studies within the Medtronic physiology lab. This role reports to the Clinical Lab Manager. The Clinical Research Specialist will independently develop and maintain study documentation, including protocols and supporting documents. The Clinical Research Specialist will manage clinical study databases and assist with the drafting, distribution and tracking of study paperwork; case report forms, and informed consents and assist in the laboratory and clinical study operations through maintenance of procedures in one or more of the following areas: production, research and development, quality control/assurance, and/or compliance/environmental safety.Location: Boulder / Denver, CO - Travel up to 15% (primarily domestic and occasionally international).Operating UnitAcute Care & Monitoring Operating Unit - Medtronic is working together with the global healthcare community to solve clinically meaningful problems, with technologies and solutions for blood oxygen management, respiratory compromise, and perioperative complications.We're committed to applying clinical and economic evidence and integrated technologies to our unmatched portfolio of therapies to develop healthcare solutions that increase patient access, improve the efficiency of procedures and deliver successful patient outcomes.We look for leaders who have a clear vision of where we are going and how to get there, bold inclusive thinkers who create new ideas and bring our best solutions forward to benefit our patients, business partners, and customers. To learn more about Inclusion & Diversity at Medtronic Click HereCareers That Change LivesOur space, the medical device and healthcare industry, is rapidly changing. It always has been that way. With remote monitoring, wearables, robotics, AR/VR, telemedicine, and much more, agility and responsiveness are key to our success. Experience what it's like to work at a company with an exciting product pipeline full of patented inventions driving innovation in the healthcare space.A Day in the LifeResponsibilities may include the following and other duties may be assigned. Oversees, designs, plans, and develops clinical evaluation research studies. Prepares and authors protocols and patient record forms. Conducts registered and non-registered clinical studies of products that have been determined to satisfy a medical need and/or offer a commercial potential. Oversees and interpret results of clinical investigations in preparation for new drug device or consumer application. Oversees and resolves operational aspects of clinical trials in conjunction with project teams and in accordance with standard operating procedures (SOP), good clinical practice (GCP) and specific country regulations, and may prepare clinical trial budgets. May be responsible for clinical supply operations, site and vendor selection. People working within region/country may also have the responsibilities that include: Represents Medtronic from a clinical research respective within the country / region and also collects feedback from local customers and authorities. Builds and maitains optimal relationships and effective collaborations with various internal and external parties. Drives local evidence dissemination & awareness. Must Have: Minimum Requirements Bachelor's degree with 2 years of clinical trials/clinical research/lab experience OR An advanced degree with 0 years of clinical trials/clinical research/lab experience Nice to Have Experience with clinical research at Medtronic Experience in pre-market/ investigational and post market studies Experience with database management, subject recruitment and consenting, data collection, and clinical reporting. Knowledge and familiarity with the operations of a medical research laboratory Ability to follow established guidelines/procedures for the preparation of various administrative forms, as well as learn new tasks independently. Able to read and interpret technical procedures and regulatory requirements. Experience in medical device clinical product trials and governing regulations. Expertise with Good Clinical Practice (GCPs) and regulatory and compliance guidelines for clinical trial. Proficient knowledge of clinical research study processes and study design. Knowledge of data analysis techniques, including basic statistical methods Leadership skills include strong communication, sense of urgency, high accountability, problem solving, quality focus, business integration acumen, and change management. Demonstrated ability to work effectively on cross-functional teams. Experience in a high-demand and fast-paced environment. Strong problem-solving skills. About MedtronicTogether, we can change healthcare worldwide. At Medtronic, we push the limits of what technology, therapies and services 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 exciting and rewarding place to be.We want to accelerate and advance our ability to create meaningful innovations - but we will only succeed with the right people on our team. Let's work together to address universal healthcare needs and improve patients' lives. Help us shape the future.Physical Job RequirementsThe 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, recruiter or local HR to understand the Work Conditions and Physical requirements that may be specific to each role. (ADA-United States of America)CompensationA 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. Learn more about our benefits here .This position is eligible for a short-term incentive plan. Learn more about Medtronic Incentive Plan (MIP) on page 6 here .The provided base salary range is used nationally (except in certain CA locations).The rate offered is compliant with federal/local regulations and may vary by experience,certification/education, market conditions, location, etc.At Medtronic, most positions are posted on our career site for at least 3-7 days.

Are you ready to elevate your career and be a part of creating the world's best desserts? Our client partners with some of North America's most iconic chains to bring people together to celebrate life's sweetest moments!We are looking for a QA Supervisor (3rd Shift) to join our team based in Colorado. This individual will be responsible for the supervision of all daily production floor activities as it relates to quality. This position will coordinate quality activities and provide leadership to ensure an effective food safety and quality management system is maintained. Provide technical support with an emphasis on customer expectations, continuous improvement opportunities, and productivity requirements. This position is responsible for the supervision of all daily production floor activities as it relates to quality and QA technicians. This position is also responsible for understanding related Quality Management Systems including SQF, HACCP, and GMP to ensure safety and quality of products.Key Responsibilities:Supervises daily activities of QA Technicians to ensure all QA tasks are carried as desiredProvides guidance regarding quality and food safety issues to ops and QA teamsCoach, train, and support the QA team to support business growthCommunicates daily with FSQA Techs regarding production schedule and QA issuesTrains FSQA Techs and performs new employee orientationsMaintain inventory of QC/lab supplies and coordinate training from suppliers or new equipment purchasedWorks with QA Manager to discipline workers as appropriateReviews and organizes operational paperwork on a daily basisSupport the execution of internal and third-party audits (e.g., customer, regulatory, GFSI, etc.) and participate in inspections; analyzing the results and deficiencies foundSupports production managers, supervisors and leads during formula changes and/or product issuesAssist with the activities of the company hold, trace, & recall program. Responsible for summarizing Hold reportsAssists in familiarizing employees with plant operations as part of company safety programsAssumes some responsibilities of the QA Manager in his/her absenceServe as backup to the Quality ManagerPerforms assignments in accordance with established Good Manufacturing Practices (GMPs), policies and proceduresSupport ops and other support teams in reducing foreign object contaminationOversee product releasesDisplays appropriate work ethics in the workplace and group setting which provides a positive influence on the production floorPerforms daily product review and customer complaint reviewsIf you'd like to hear more about this opportunity and others we are currently working on, please contact Jeff Fee at [email protected]: 135.24JFTechnical Qualifications:BS degree or equivalent experience in a food manufacturing environmentPrevious knowledge working in food production Quality Assurance department2+ years of supervisory experienceMust have a flexible schedule including working weekends, as necessaryExcellent verbal and written communication skillsIntermediate to advanced proficiency using Microsoft OfficeMust have reliable transportationAbility to work in a team environmentMaintains good housekeeping and clean work areas in assigned spaceIf you'd like to hear more about this opportunity and others we are currently working on, please contact Jeff Fee at [email protected]: 135.24JF