Principal Quality Systems Specialist
Job Description
At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.
A Day in the Life
At Medtronic, we’re driven by our Mission to alleviate pain, restore health, and extend life. As a Principal Quality Systems Specialist, you’ll play a key role in ensuring the integrity of our quality systems, supporting regulatory compliance, and helping us deliver innovative medical technologies that transform lives.
In this role, you will provide leadership and subject matter expertise in the development, implementation, and continuous improvement of our Quality Systems. You will work cross-functionally to ensure compliance with internal policies and procedures as well as global regulatory requirements. This position offers the opportunity to influence and shape quality culture while supporting strategic and operational initiatives.
Key Responsibilities:
- Provide oversight for the development and maintenance of quality systems, programs, processes, and procedures to ensure ongoing compliance with Medtronic policies and global regulatory requirements.
- Interpret and apply regulatory, governmental, and internal policies to ensure adherence and guide others in compliance efforts.
- Partner with operational teams to assess processes, identify areas for improvement, and implement corrective actions to meet quality and regulatory standards.
- Lead preparation for audits and inspections, including strategy development, readiness activities, hosting, and follow-up, ensuring timely resolution of findings.
- Coordinate documentation and reporting activities such as Corrective and Preventive Actions (CAPAs), audit responses, and quality system metrics.
- Support legal and regulatory requests in response to government investigations or litigation as needed.
- Drive consistency and excellence by facilitating global standards and sharing best practices across sites and teams.
- Champion a culture of quality, continuous improvement, and proactive compliance across the organization.
Must Have: Minimum Requirements
- Bachelor’s degree with a minimum of 7 years of relevant experience OR Advanced degree with 5 years or relevant experience
Nice to Have: Preferred Qualifications
- Experience in a regulated industry (e.g., medical device, pharmaceutical, or life sciences).
- Demonstrated knowledge of global regulatory standards (e.g., FDA QSR, ISO 13485, MDR).
- Experience leading audits or inspections and working with regulatory bodies.
- Strong project management and cross-functional collaboration skills.
- Excellent verbal and written communication skills.
- Ability to influence without authority and drive alignment across teams.
- Experience working in a global matrix organization.
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.
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.
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
About Medtronic
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.
Learn more about our business, mission, and our commitment to diversity here.
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.
Company Information
Location: Dublin, Ireland
Type: Hybrid