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2000060G Requisition #
Thanks for your interest in the Medical Writing Program Manager position. Unfortunately this position has been closed but you can search our 398 open jobs by clicking here.
Must Have (Minimum Requirements):

To be considered for this role, the minimum requirements must be evident on your resume.


Bachelor’s degree required and a minimum of 5 years of experience in scientific/medical writing (e.g., clinical research/regulatory affairs/medical affairs) 


advanced degree with a minimum of 3 years of experience in scientific/medical writing (e.g., clinical research/regulatory affairs/medical affairs) 


Nice to Have (Preferred Qualifications):

  • Masters or PhD degree(s) in biomedical sciences or technical disciplines.
  • Direct expertise leading and managing a team of professionals, and experience hiring, coaching and development team members. 
  • Specific experience with clinical research and publications in cardiovascular disease and treatment. 
  • Internal to Medtronic strongly preferred. Medtronic or Medical device industry experience or related industry experience that demonstrates mastery and in-depth knowledge of medical device and/or combination product trials and regulations. Advanced experience in medical writing and publication development for medical device regulatory approval.
  • Direct experience demonstrating knowledge of medical and/or scientific writing within a medical device or related industry, preferably with writing of Clinical Evaluation Reports (CER)
    • Broad expertise in collaborating on clinical and regulatory documents as well as a solid understanding of EU guidance and regulations. 
    • Strong knowledge of regulatory guidance relative to Clinical Evaluation Reports, and the essential requirements for safety and performance of Medical Devices as defined in Annex I of the Medical Device Directive 93/42/EEC and Annex I of the Active Implantable Medical Device (AIMD) Directive 90/385/EEC,(Annex  I Section 6a and Annex X (MDD) / Annex 1 Section 5a and Annex 7 AIMD), the MEDDEV and EN ISO 14155 and EU Medical Device Regulation.
    • Strong knowledge of medical terminology and scientific literature searches.
  • Strong complex project leadership skills and excellent interpersonal communication skills; experience driving outcomes and balancing competing priorities.
  • Demonstrated ability to successfully interact with a variety of functions and levels within an organization. 
  • Experience with Project Management principles, concepts, practices and standards, as well as process improvement and/or system harmonization initiatives
  • Experience working in matrixed teams responsible for influencing and communicating at all levels within the organization
  • Experience implementing initiatives through effective influence management skills at multiple levels in the organization
  • Clear track record of demonstrated ability to develop solutions to complex problems that require regular use of ingenuity and creativity and ensures that solutions are consistent with organization objectives and goals.

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 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. (ADA-United States of America)


Travel is required up to 25%, may be domestic and/or international travel.

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Change Begins With You

We look for bold ideas and fresh insights - that's what drives innovation. Come drive the future of healthcare with us.


The opportunity to invent. The benefit of joining a leader. The power to improve lives. You’ll find all that and more here.

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Bring life-changing solutions to those who need them. Be rewarded for rewarding work.

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Join us in our challenge to make global healthcare more affordable and accessible. Your insight and oversight will help us create solutions that change the world.

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Medtronic Mission.

Our mission “to alleviate pain, restore health, and extend life” is more than a statement. It’s a belief that our employees live every day.

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Alyse is an Engineering Program Manager for Neuromodulation in Minneapolis, Minnesota.

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Our employees come from varied backgrounds with a common goal—changing lives.

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The mission to improve access to healthcare globally is something we are all very proud to work hard toward achieving. Great people, fun atmosphere, big city salaries. The CEO is fantastic - he is a very clear communicator of the mission and is truly dedicating his life to achieving it.
Smart and committed coworkers. Mission driven. Good benefits. Good long term career opportunities. Company is large enough that you can always find interesting projects to work on.
Knowing that everyday your work helps to save lives makes it great place to work. Training on lean practices, quality and other. Excellent peers.


Be part of one of the world’s leading medical technologies and solutions companies.