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You will be updated with latest job alerts via email$ 113600 - 170400
1 Vacancy
At Medtronic you can begin a life-long career of exploration and innovation while helping champion healthcare access and equity for all. Youll lead with purpose breaking down barriers to innovation in a more connected compassionate world.
Act boldly. Compete to win. Move with speed and decisiveness. Foster belonging. Deliver resultsthe right way. Thats the Medtronic Mindset our cultural norms. Our brand is rooted in action not just words. The Medtronic Mindset defines the expectations of our culture. Every person here plays a role in bringing it to life. We recognize your extraordinary potential to ensure future generations live better healthier lives.
The Principal Compliance Audit Specialist focus will be primarily medical device software product security and risk management. We look for leaders who have a clear vision of where we are going and how to get there bold inclusive thinkers who create new ideas and bring our best solutions forward to benefit our patients business partners and customers.
Responsibilities may include the following and other duties may be assigned.
Must have experience and knowledge working with regulated medical devices and cybersecurity requirements.
Manage and oversee internal audit activities which may include conducting and/or overseeing audits investigations and/or interviews; and preparing corresponding reports and documents.
Coordinate and/or complete internal assessments and/or audits in accordance with regulatory standards which may include US and/or international regulatory agencies/authorities.
Interpret and implement applicable regulations as they apply to products processes practices and procedures.
May counsel stakeholders about these requirements as necessary.
Ensure compliance with internal and external regulatory agencies which may include investigating and resolving compliance violations questions or concerns.
Analyze audit data and present findings to management and/or regulatory bodies in support of Corrective Action Plans which may include coaching business partners on compliance gaps data and/or resulting corrective actions.
Own development of training and awareness programs for SaMD SiMD and product security designed to increase auditor awareness and knowledge of requirements.
Remain informed on Regulatory requirements for Software and Product Security to identify gaps in medical device software.
Provide detailed functional knowledge and maintain insight to current industry best practices and how they can be applied to Medtronic.
Explore new tools and techniques to recommend for other team members to audit product security.
Identify opportunities for product security enhancement.
Possess understanding of Software Bill of Material (SBOM) development and maintenance for the purposes of vulnerability monitoring.
Possess an understanding of scoring methodologies for security threats like the common vulnerability scoring (CVSS) and apply appropriately.
Document and communicate recommended security controls and deficiencies.
Provide detailed functional knowledge and maintain insight to current industry best practices and how they can be applied to Medtronic.
Contribute to company standards and policies related to product security risks.
Enable strong partnerships across the organization to drive best-in-class product security mechanisms.
Analyze complex issues and significantly improve change or adapt existing methods.
Show creativity and innovation in all aspects of your responsibilities.
Expected travel: 20-25%
Onsite
At Medtronic we bring bold ideas forward with speed and decisiveness to put patients first in everything we do. In-person exchanges are invaluable to our work. Were working a minimum of 4 days a week onsite as part of our commitment to fostering a culture of professional growth and cross-functional collaboration as we work together to engineer the extraordinary.
Must Have: Minimum Requirements
To be considered for this role please ensure the minimum requirements are evident in your applicant profile.
Bachelorsdegree with 7 years of work experience in Quality or regulated industry OR Advanced degree with 5years of work experience in Quality or regulated industry
Nice to Have
Security Certifications (i.e. CISSP CEH CISA CISM Security GSEC OSCP etc.)
Firsthand experience assessing the embedded security of regulated or safety critical devices.
Experience in Quality/Compliance and/or Audit with medical device requirements (e.g. MDSAP EU MDR ISO 13485).
Experience with cybersecurity requirements.
TUV; EU MDR / MDCG.
IMDRFs Principles and Practices for Medical Device Cybersecurity.
ENISA EU Cybersecurity Act.
European Commissions Guidance on Cybersecurity of Medical Devices (MDCG).
United States FDA Pre-Market and Post-Market Guidance.
TIR 57 and TIR 97.
ISO 80001-2 series and 14971.
Experience auditing Quality Systems to global requirements.
Quality System Lead Auditor certified.
Prior FDA or NB auditor experience.
Experience performing hardware and software penetration testing.
Understanding of the security development process and product development process.
Experience in leading small teams.
Knowledge in risk management and assessment methodologies security frameworks and relevant global regulations.
Strong capability to research and evaluate emerging technologies.
A solid familiarity of threat modeling vulnerability scanning tools and common attack routes is essential.
Demonstrated ability to be flexible and take a proactive approach to managing change.
Experience working in a regulated environment and/or a formal quality system.
Occasional after-hours availability to accommodate different regional and global partners.
A solid familiarity of threat modeling vulnerability scanning tools and common attack routes is essential.
Medical device engineering experience.
Strong technical and troubleshooting skills.
Strong capability to research and evaluate emerging technologies
Preference is given to those with relevant product security or engineering experience.
Strong in interpersonal communication and demonstrate a collaborative work style.
Comfortable working in an ambiguous environment.
Innovative thinker: ability to think outside of the current norms and processes.
Independent self-starter
Strong communication and collaboration skills.
Solid writing and presentation skills.
Interest in novel applications of technology.
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.
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 insuranceHealth Savings AccountHealthcare Flexible Spending AccountLife insurance Long-term disability leaveDependent daycare spending accountTuition assistance/reimbursement andSimple 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 matchShort-term disabilityPaid time offPaid holidaysEmployee Stock Purchase PlanEmployee Assistance ProgramNon-qualified Retirement Plan Supplement (subject to IRS earning minimums) andCapital 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
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 95000 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 findhere 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.
Required Experience:
Staff IC
Full-Time