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Careers That Change Lives

A career at Medtronic is like no other. We're purposeful. We're committed. We're driven by our Mission to alleviate pain, restore health, and extend life for millions of people worldwide. We believe career growth and development is about learning and stretching yourself to grow your expertise and navigate your career. We offer award-winning programs to accelerate your development and growth, and our size, scope, and market leadership help you explore career opportunities and grow as we grow.  Medtronic walks the walk, creating an inclusive culture where you can thrive. We believe that when people from different cultures, genders, and points of view come together— everyone wins.

We are seeking a Senior Medical Safety Specialist (Diabetes) for a fully remote opportunity providing medical expertise and assessment to support patient safety throughout the product lifecycle as both an advocate for patient safety and in support of safe and effective use of Diabetes products and therapies. The Diabetes product portfolio includes insulin pumps, continuous glucose monitors, insulin pens, consumables, and multiple applications. The Senior Medical Safety Specialist provides technical and clinical information regarding product usage and performance -- specifically as it relates to patient safety -- on a range of medical safety activities of varying complexity in collaboration with Medical Safety team members and other functions, including Regulatory, Quality/Post-Market vigilance, Risk Management, Complaint Handling, Product Development, and Medical Affairs. They primarily interact with medical safety team members (and other functions as needed) to share information or gain input to support decision-making. They may occasionally interact in a supportive role with external physicians.

A Day in the Life

You will apply your medical knowledge, clinical expertise, and product knowledge to support patient safety to support the following:

• Leverage medical knowledge and advocate for patient safety by providing medical safety input to internal functions and business processes across the product life cycle.

• Evaluate events and potential safety signals identified through Quality, Clinical, and Regulatory related business unit processes.

• Author high-quality and accurate safety assessments per business unit processes, leveraging complaint data, literature, registries, or other data sources as appropriate.

• Critically assess and escalate newly identified safety issues (suspected increase in severity and/or frequency of known events or new events with a causal relationship to the device) per business unit processes for investigation assessment and action.

• Assist with obtaining input from external medical and subject matter experts on safety matters.

• Complete qualitative and quantitative assessments of post-market adverse events, medical significance, and recommendations for inclusion in regulatory annual reports.

• Provide evidence-based medical safety input, education and/or response to safety inquiries from internal or external stakeholders (e.g., external medical personnel or other third parties, including regulatory agencies or health care organizations).

• Acquire and maintain proficient knowledge of assigned products and therapies, such as device design and function, product labeling, indications, mechanism of action, care pathways, and overall safety profile (i.e., hazards and harms).

• Actively acquire and maintain knowledge of relevant scientific literature associated with assigned devices/therapies.

• Acquire and maintain advanced knowledge of applicable business unit policies/procedures, and relevant regulatory requirements and guidelines (e.g., ISO 14971, Application of Risk Management, ISO 13485, Quality Management Systems).

• Maintain an advanced understanding of key business processes involving Medical Safety (e.g., risk management, post-market vigilance).

• Work effectively across the matrix.

• Develop solutions and lead opportunities to advance and improve safety practices.

• May lead other projects that span outside of Medical Safety, as assigned in part or in entirety.

• Lead and influence evidence-based medical decision-making across the matrix organization.

• Provide strategic input and influence business strategies to optimize Medical Safety value.

• Interpret, analyze, and effectively communicate medical assessment across a variety of levels and audiences.

• Adapt verbal and written communication style to situational context.

• Adapt to changing priorities and work demands.

• Travel is required. Less than 10%.

Must Have: Minimum Requirements

• Bachelor's degree in Nursing required.

• Licensed healthcare professional or certified personnel with clinical knowledge and relevant patient care experience (e.g., RN, MD, PA, NP) including a minimum of four years of clinical experience in Diabetes care, or if an advanced degree (Master’s or above), a minimum of two years of clinical experience in Diabetes.

• At least four years of experience with insulin pump therapy and continuous glucose monitoring.

Nice to Have

• Ability to perform patient assessments.

• 3+ years experience in the medical device industry preferred.

• Basic ability to understand and apply practical medical and product knowledge in a competent manner for Medical Safety activities.

• Able to make competent, risk-based, and timely medical safety decisions based on insightful analysis of critical information; able to balance analysis with decisiveness.

• Able to understand scientific/technical concepts and function of medical devices.

• Excellent verbal and written communication skills to effectively convey messages and influence diverse stakeholders.

• Solid medical background with the ability to apply complex disease states and different treatment outcomes and complications specific to the cardiac dysrhythmia population.

• Versatile learner, able to quickly and effectively integrate new information and skills.

• Divergent thinker with solid critical thinking and problem-solving skills. Must be able to reach determined goals by prioritizing workload effectively and independently.

• High attention to detail and accuracy; able to work independently with minimal supervision; accountable for outcomes.

• Able to develop trusted relationships and collaborate with peers, co-workers, and key functional partners.

• Good understanding of regulatory guidance from European Medicines Evaluation Agency (EMEA), Food and Drug Administration (FDA).

• Proficient in Microsoft Office applications including Microsoft Word and Excel and ability to learn new document systems/solutions.

About Medtronic

Together, 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 Requirements

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. 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.

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. Learn more about our benefits here (http://benefits.medtronic.com/) .

This position is eligible for a short-term incentive plan. Learn more about Medtronic Incentive Plan (MIP) 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 experience, certification/education, market conditions, location, etc.

Min Salary

103200

Max Salary

154800

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.