Regulatory Affairs Specialist
$74.4k - $111.6kMedtronic
We anticipate the application window for this opening will close on - 17 Aug 2026
Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first - developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact.
A Day in the Life
Medtronic's Access and Instruments Operating Unit develops technologies that support surgical access and enable precise, efficient procedures across a range of care settings. The portfolio includes products and solutions designed to help clinicians access the surgical site, perform procedures with greater control, and support workflow in the operating room. As part of Medtronic's broader mission, this team is focused on advancing innovative tools that help improve procedural outcomes and support high-quality patient care.
As a Regulatory Affairs Specialist in the Access and Instruments Operating Unit, you will play an important role in supporting innovative medical technologies throughout the product lifecycle. You will partner with cross-functional teams to prepare regulatory documentation, assess the impact of product changes, maintain regulatory systems, and help ensure compliance with global requirements.
This role is ideal for someone who thrives in a collaborative environment, enjoys navigating complex regulatory requirements, and is energized by the opportunity to support technologies that improve patient care.
In this role, you will:
Partner with multidisciplinary teams to communicate regulatory requirements and support regulatory strategy.
Provide regulatory input to product development, lifecycle planning, and change control activities.
Assess the regulatory impact of proposed design, labeling, manufacturing, and process changes.
Prepare, review, and coordinate documentation for regulatory submissions, renewals, registrations, and related filings.
Support audits, inspections, and regulatory authority interactions as needed.
Participate in risk management activities and help ensure regulatory considerations are addressed appropriately.
Monitor and support tracking systems used to manage regulatory deliverables and documentation.
Stay current on applicable regulations, standards, and guidance documents relevant to assigned products and markets.
Collaborate with internal stakeholders to help resolve issues, manage priorities, and keep regulatory activities on track.
Contribute to process improvements and help strengthen regulatory practices across the organization.
To be considered for this role, you must have:
Bachelor's degree required
Minimum of 2 years of relevant experience, or advanced degree with a minimum of 0 years of relevant experience.
Preferred qualifications include:
Experience with U.S. FDA and international regulatory requirements for medical devices
Familiarity with EU MDR, MDD, ISO 13485, ISO 14971, and related standards
Experience supporting regulatory submissions, audits, or inspections
Strong written and verbal communication skills
Strong organizational skills with the ability to manage multiple priorities
Experience collaborating in a cross-functional, fast-paced environment
Familiarity with medical device product development or lifecycle management
RAC certification or progress toward certification
Experience working with Notified Bodies or global regulatory agencies
For Baccalaureate degrees earned outside of the United States, a degree that satisfies the requirements of 8 C.F.R. § 214.2(h)(4)(iii)(A) is required.
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.
U.S. Work Authorization & Sponsorship
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.
?
Recruitment Fraud Alert
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 View email address on click.appcast.io .
?
Benefits & Compensation
Medtronic offers a competitive Salary and flexible Benefits Package
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.
Salary ranges for U.S (excl. PR) locations (USD):$74,400.00 - $111,600.00
This 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).
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.
We 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 95,000+ 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.
We change lives . Each team member, each day, helps to improve and redefine how the world treats the most pressing health conditions, from heart disease to diabetes. Our industry leadership comes from the passion and ingenuity of our people. That's who we are. Working alongside one another, we use science, medicine, and a profound understanding of the human body to build extraordinary technologies that can transform lives.
We build extraordinary solutions as one team . With one Medtronic Mindset defining how we work. Speed and decisiveness run through our DNA. Diverse perspectives inspire our bold answers to any challenge that comes our way. And we deliver results the right way, breakthrough after patient breakthrough.
This life-changing career is yours to engineer . By bringing your ambitious ideas, unique perspective and contributions, you will...
Build a better future, amplifying your impact on the causes that matter to you and the world
Grow a career reflective of your passion and abilities
Connect to a dynamic and inclusive culture that welcomes the challenge of life-long learning
These commitments set our team apart from the rest:
Experiences that put people first . Respect for people is the hallmark of our humanity. It fuels our team to positively impact even a single life. And it means we put our people first at Medtronic as well, creating a culture of belonging and always pushing to get you the career-building resources you need.
Life-transforming technologies . No matter your role, you contribute to technologies that transform lives. What we build empowers patients to live life on their terms.
Better outcomes for our world . Here, it's about more than the bottom line. Our Mission to improve human welfare drives us. We advance healthcare, society, and equity with every design, inside and outside our walls.
Insight-driven care . Fresh viewpoints. Cutting-edge AI, data, and automation. You're shaping the future of healthcare technology and defining the next generation of breakthroughs in care
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.
For sales reps and other patient facing field employees, going into a healthcare setting?is considered an essential function of the job and we expect our employees to comply with all credentialing requirements at the hospitals or clinics they support.
This employer participates in the federal E-Verify program to confirm the identity and employment authorization of all newly hired employees. For further information about the E-Verify program, please click here ( .
For updates on job applications, please go to the candidate login page and sign in to check your application status.
If you need assistance completing your application please email View email address on click.appcast.io
To request removal of your personal information from our systems please email View email address on click.appcast.io
- ...Job Title: Regulatory Affairs Specialist III Location: Maplewood, MN Duration: 18 Months+ Pay: $50/hr. on W2 Description : When you're part of ***, you'll do challenging work while collaborating with a team that values performance, quality, innovation,...SuggestedMonday to FridayFlexible hours
$50 per hour
...Regulatory Affairs Specialist III Our client, a leading organization in the life sciences and healthcare industry, is seeking a Regulatory Affairs Specialist III to join their team. As a Regulatory Affairs Specialist III, you will be part of the Regulatory Affairs &...SuggestedWeekly payTemporary workFlexible hours- .... • Conduct evaluations of chemical formulations to support regulatory compliance determinations. • Administer regulatory label and... ...Required Skills & Experience • 4+ years of Regulatory Affairs experience in a corporate environment • Bachelor's degree with...Suggested
- ...Position Summary This role is ideal for a regulatory professional with strong experience in FDA, Health Canada, and EU medical device requirements. The Regulatory Affairs Specialist will maintain global registrations and technical documentation, support audits, manage...SuggestedWork at office
$45 - $55 per hour
...Regulatory Affairs & Product Stewardship Specialist Adecco Healthcare & Life Sciences Opportunity Location: Maplewood, MN Type: 6-Month Contract-to-Hire Opportunity Pay Rate: $45-$55/hour (based on experience) Schedule: Monday-Friday | 8:00 AM-5:00 PM...SuggestedHourly payContract workTemporary workLocal areaMonday to FridayFlexible hours$74.4k - $111.6k
...Regulatory Affairs Specialist Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first...H1bWork at officeLocal areaImmediate startFlexible hours$60k - $120k
...Regulatory Operations Specialist I Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical...For contractorsWork experience placementWorldwideShift work$80.9k - $127.05k
What Regulatory Affairs contributes to Cardinal Health Regulatory provides regulatory affairs and product development consulting services to... .... Job Summary The Principal Regulatory Affairs Specialist will support the Medical Solutions Regulatory affairs team....Temporary workWork experience placementLocal areaRemote workFlexible hours$142.8k - $196.35k
...Principal Regulatory Affairs Specialist – Solventum Impact You’ll Make in this Role Serve as regulatory affairs lead on cross‑functional teams, owning product‑line regulatory submissions and registrations for the Dental Solutions business in global markets. Drive regulatory...Remote workWork visaFlexible hours$50 - $53 per hour
...Job Title: Senior Regulatory Affairs Specialist Location: 1225 Old Highway 8 NW, Saint Paul, MN 55112 Duration: 6 Months Work Arrangement: 100% Onsite Pay Range: $50 - $53 per hour (W2) We are seeking a Senior Regulatory Affairs Specialist to join one of our leading healthcare...Hourly payWork at office- ...Principal Regulatory Affairs Specialist The Principal Regulatory Affairs Specialist is responsible for developing and implementing regulatory strategies across projects, processes, and/or products. This individual partners with internal stakeholders and external consultants...Worldwide
$92k - $138k
...Senior Regulatory Affairs Specialist The Interventional Cardiology Therapies (ICT) portfolio provides innovative, minimally invasive cardiovascular technologies designed to help physicians diagnose and treat complex heart and vascular conditions, improve patient outcomes...Temporary workH1bWork at officeLocal areaImmediate startFlexible hours- Job Description: Highly experienced Principal Regulatory Affairs Specialist to lead and support global post-market regulatory compliance activities within the Interventional Cardiology and Vascular Therapies Division. This role is responsible for ensuring compliance with...
$90k - $121.3k
...Advisory Services Officer who will serve as the primary Compliance Department point of contact for assigned lines of business and/or regulatory topics. This individual is responsible for pro-actively advising on all applicable federal and state regulatory compliance...Work experience placementWork at office- ...Regulatory Affairs Specialist III – Maplewood, MN (Hybrid) Contract Duration: 18 months (possible extension). Pay Rate Range: $45.00/hr – $55.00/hr on W2. Work Authorization: Only U.S. Citizen or Green Card holder. About VARITE VARITE is an American‑headquartered life...Contract work
- ...Regulatory Affairs Consultant (Contract-to-Hire) We are seeking a Regulatory Affairs Consultant for a 6-month contract-to-hire opportunity supporting Class II medical devices, with a strong focus on SaMD. 6-month contract-to-hire 40 hours per week Hybrid: 2–3 days onsite...Contract work
- ...The Regulatory Affairs Specialist will play a key role in supporting regulatory strategy and compliance throughout the product lifecycle. Reporting to the Global Product Director, this individual will partner closely with Engineering, Quality, Operations, Manufacturing...InternshipWork at office
- ...Our client, a leader in the healthcare industry, is seeking a Regulatory Affairs Specialist to join their team. As a Regulatory Affairs Specialist, you will be part of the Regulatory Affairs Department supporting global post-market compliance activities. The ideal candidate...Weekly payTemporary workFlexible hours
- ...Regulatory Affairs Specialist II - (RAS2.1) Company Description Stereotaxis is the global leader in innovative robotic technologies designed to enhance the treatment of arrhythmias and perform endovascular procedures. Its mission is the discovery, development and delivery...Work at office
$71k - $112k
...The Regulatory Affairs Specialist I supports regulatory activities to help ensure Philips Image Guided Therapy Devices are safe, effective, and compliant with applicable global regulatory requirements. This role also provides an excellent opportunity to develop expertise...Full timeWork at officeLocal areaWork visaRelocation package3 days per week- U.S. Bank in Minnesota seeks a contract-driven compliance professional for a structured finance environment. You will interpret legal agreements, monitor compliance, and ensure systems reflect contractual obligations while resolving issues independently. This role suits...Contract work
$20 - $30 per hour
## ML Title 31 Compliance Specialist FT/DA $20 to $30Applylocations: Grand Casino Mille Lacstime type: Full timeposted on: Posted Yesterdayjob... ..., complete, and readily available for potential audits or regulatory examinations.* Ensure that all necessary forms, such as CTRs...Work at office$60k - $90k
Job Description At Norton Rose Fulbright, people thrive because of a shared commitment to quality, unity and integrity. The highly regarded law firm consistently receives recognition from Great Place to Work and Top Workplaces, two companies that specialize in assessing...Full timeFor contractorsWork at officeRemote workWorldwideFlexible hours$120k - $180k
...performance, foster an environment of belonging, and collaborate to inspire as we engineer the extraordinary. The Principal Regulatory Affairs Specialist will play a key role in launching new products and sustaining the Pain Interventions product portfolio. As a core member...Full timeH1bWork at officeLocal areaImmediate startWorldwideFlexible hours$92k - $138k
...back active lives through the restorative therapies that we provide. Therefore, we are looking for a passionate Senior Regulatory Affairs Specialist who has direct experience submitting regulatory submissions for both the Americas and the EU. Role OverviewThe Senior Regulatory...Full timeH1bLocal areaImmediate startWorldwideFlexible hours- Our client, a leading organization in the safety and regulatory compliance industry, is seeking a SAF Regulatory/Environmental Analyst... ...Regulatory/Environmental Analyst, you will be part of the Regulatory Affairs department supporting certification and compliance efforts...Weekly payTemporary workLocal areaFlexible hours
- ...caps, captive carrier limitations, or opaque lead structures? We are expanding our network of established financial protection specialists. This 1099 entrepreneurial partnership is tailored for self-starting professionals who want to maximize their earning potential...Contract workWork at officeImmediate startRemote work
$44.8k
Maximus is searching for an IT Auditor role supporting upcoming federal OPTN work, contingent upon contract award. In this role, you will help safeguard the integrity, reliability, and security of critical technology systems by planning and executing audits across information...Contract work- ...Senior Regulatory Affairs Specialist – Medical Devices About the Role We are seeking a Senior Regulatory Affairs Specialist to support global regulatory activities for medical devices. This role partners with cross‑functional teams to develop regulatory strategies, prepare...
- IT Compliance Analyst Little Canada MN 12+ months contract to hire Pay range: $36 - $38/hr on W2 Our Fortune 500 client (One of the world's largest Medical Device companies) in Little Canada MN is looking for hardworking, motivated talent...Contract work
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Regulatory Affairs Specialist. Be the first to apply!
- compliance analyst Saint Paul, MN
- regulatory compliance analyst Saint Paul, MN
- coding compliance specialist Saint Paul, MN
- compliance associate Saint Paul, MN
- regulatory compliance specialist Saint Paul, MN
- regulatory affairs specialist Saint Paul, MN
- compliance consultant Saint Paul, MN
- healthcare compliance officer Saint Paul, MN
- medicare compliance specialist Saint Paul, MN
- cybersecurity policy and compliance analyst Saint Paul, MN

