16h ago
New
$175,200.00 - $262,800.00/yr

Senior Software Manager - CRDN

United StatesUnited States·Minneapolissenior
Other
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Quick Summary

Key Responsibilities

Lead a team of software engineers for capital equipment ((RF Generator) and accessory software, this encompasses development and support of firmware,

Technical Tools
Other
We anticipate the application window for this opening will close on - 3 Nov 2026

What We Offer

~2 min read

The Senior Software Engineering Manager will have full life cycle responsibility for a software product in the ICT portfolio and oversight of a team of software engineers who develop and support firmware, embedded, GUI and application software for stand-alone medical device and accessory digital solutions. You will be responsible for department processes, talent recruitment, performance and development, resource planning and prioritizing and directing the responsibilities of your team.


The Senior Software Manager partners closely with Product Teams leadership across entire software development lifecycle (SDLC) of products. In general, the following responsibilities apply for the Senior Software Manager role. This includes, but is not limited to the following:


✓Lead a team of software engineers for capital equipment ((RF Generator) and accessory software, this encompasses development and support of firmware, embedded software and GUI for medical device; along with Windows applications and Cloud services.
✓Lead the Scrum Team through the SDLC for medical devices following IEC 62304/82304.
✓Work with different stakeholders and Cross-functional team to prioritize team work according to business needs.
✓Collaborate with stakeholders to gather input, provide updates, and align product strategies with their needs and expectations.
✓Decompose and elaborate on feature requirements and management of team backlog
✓Guide SW development scrum team in sprint and increment planning, championing and supervising value-focused capabilities.
✓Participate in Risk Assessment and requirements development.
✓Participate in the documentation of the software including architecture and design detail, unit testing, defect tracking and reports.
✓Accountable for the quality, robustness, predictability, and completeness of the team’s output, including tracking and reporting software quality metrics.
✓Accountable for your team’s compliance with internal design controls and medical device regulations and standards
✓Prepare team members for certification and regulatory audits. May represent the team’s work in audits.
✓Drive departmental excellence, proficiency, best practice, and consistency across project teams.
✓Anticipate the need for new development tools, methods, technologies, and processes.
✓Represent your team to the wider organization.
✓Mentor and coach your team members.

  • Experience building medical device software
  • Experience building Windows based applications and Cloud services
  • Experience leading agile software development teams

Requirements

~1 min read

 

MUST HAVE - MINIMUM REQUIREMENTS:

 

 

  • Bachelor’s degree in computer engineering, software engineering, computer science, electrical engineering, or a related technical discipline and minimum of 7 years of work technical experience OR advanced degree in computer engineering, software engineering, computer science, electrical engineering, or a related technical discipline with 5 years of technical work experience, and 5 years of managerial experience

 

 

Nice to Have

~1 min read
  • Familiarity with FDA submissions, design history files (DHF), and technical documentation
  • Experience in software architecture design, writing design documents, creating flowcharts, layouts, diagrams, charts.
  • Agile SAFe training/experience
  • Excellent collaboration skills across engineering, quality, and regulatory teams
  • Pragmatic decision‑making that balances compliance, security, and delivery velocity

 

Responsibilities

~1 min read

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.

At Medtronic, we are committed to fostering an environment where employees can thrive and make a meaningful impact. In alignment with our enterprise-wide workforce planning approach, U.S. work authorization sponsorship (H-1B, TN, J, etc.) is offered exclusively for Principal-level roles and above, where specialized expertise aligns with long-term business needs. Roles below the Principal level require candidates to possess unrestricted U.S. work authorization at the time of hire and for the duration of employment.

‌

We are aware of phishing scams targeting job seekers. Please keep the following in mind: 


Apply only through official Medtronic channels. All legitimate Medtronic recruiting communications come from approved Medtronic platforms and official @medtronic.com email addresses. 


Medtronic will never ask for payment or sensitive personal information (such as bank account or Social Security details) during early stages of the hiring process. Any such requests are not legitimate. 


If you receive a suspicious message claiming to be from Medtronic, do not respond, click links, or open attachments. 


If you have any questions, concerns regarding the authenticity of a communication alleged to have been made by or on behalf of Medtronic, please contact us immediately at AskHR@medtronic.com. 

‌

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).

The following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance, Health Savings Account, Healthcare Flexible Spending Account, Life insurance, Long-term disability leave, Dependent daycare spending account, Tuition assistance/reimbursement, and Simple Steps (global well-being program).

 

The following benefits and additional compensation are available to all regular employees: Incentive plans, 401(k) plan plus employer contribution and match, Short-term disability, Paid time off, Paid holidays, Employee Stock Purchase Plan, Employee Assistance Program, Non-qualified Retirement Plan Supplement (subject to IRS earning minimums), and Capital Accumulation Plan (available to Vice Presidents and above, or subject to IRS earning minimums).

 

Regular employees are those who are not temporary, such as interns.  Temporary employees are eligible for paid sick time, as required under applicable state law, and the Employee Stock Purchase Plan. Please note some of the above benefits may not apply to workers in Puerto Rico.

 

Further details are available at the link below:

Medtronic benefits and compensation plans

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.


If you are applying to perform work for Medtronic, Inc. (“Medtronic”) in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. Medtronic will consider for employment qualified job applicants with arrest or conviction records in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.

Location & Eligibility

Where is the job
Minneapolis, United States
On-site at the office
Who can apply
US

About this job

Pay per year
$175,200–$262,800 a year
221% above the $68,120 median for Other jobs on Jobera (125,697 salaries).
Who can apply
United States
Posted
Today
Employer
has 2,154 open jobs on Jobera in 58 countries.

Listing Details

Posted
October 27, 2026
First seen
October 27, 2026
Last seen
October 27, 2026

Posting Health

Days active
0
Repost count
0
Trust Level
68%
Scored at
October 27, 2026

Signal breakdown

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Employees
10,001+
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Senior Software Manager - CRDN$175,200.00 - $262,800.00