Senior Regulatory Compliance Specialist Medical Device
$70.6k - $141.2kOracle
Job Description
Oracle Health is a comprehensive suite of healthcare technology solutions designed to help organizations advance patient care, improve operational efficiency, and enhance caregiver experiences. Building on Oracle’s global expertise in cloud technology, data management, and analytics, Oracle Health delivers integrated electronic health records (EHR), population health tools, and data-driven insights for hospitals, clinics, and health systems. By connecting data and workflows across the continuum of care, Oracle Health empowers providers to make informed decisions, streamline processes, and drive better health outcomes.
The Senior Compliance Specialist provides guidance to cross-functional teams on medical device quality system compliance, with a focus on quality system support for CE marking processes and requirements under the EU Medical Device Regulation (EU MDR).
Responsibilities
The Senior Compliance Specialist will provide quality system support through conformity assessment procedures, technical documentation preparation, medical device file development and maintenance, risk management, and post-market surveillance for medical device market access. The Senior Compliance Manager coordinates and assist with both internal and external audits, including Notified Body audits related to CE marking, and helps manage corrective and preventive actions (CAPA). They assist with monitor compliance with changing European regulatory requirements and act as a subject matter expert on EU market authorization.
The incumbent maintains up-to-date knowledge relevant regulations, works collaboratively with cross-functional teams to meet quality objectives, analyses HQMS data and metrics for management reporting, and supports supplier quality management activities.
Key Skills and Requirements
5 plus years of relevant experience
BA/BS or advanced degree preferred
Have an understanding of quality management system standards and risk management.
Excellent written and verbal communication skills.
Project Management Skills
Ability to adjust and adapt to changing priorities in a dynamic environment.
#LI-SP1
Disclaimer:
Certain U.S. based or U.S. customer or client-facing roles may be required to comply with applicable requirements, such as immunization/occupational health mandates, and/or drug testing requirements.
Range and benefit information provided in this posting are specific to the stated locations only
US: Hiring Range in USD from: $70,600 to $141,200 per annum. May be eligible for bonus and equity.
Oracle maintains broad salary ranges for its roles in order to account for variations in knowledge, skills, experience, market conditions and locations, as well as reflect Oracle's differing products, industries and lines of business.
Candidates are typically placed into the range based on the preceding factors as well as internal peer equity.
Oracle US offers a comprehensive benefits package which includes the following:
Medical, dental, and vision insurance, including expert medical opinion
Short term disability and long term disability
Life insurance and AD&D
Supplemental life insurance (Employee/Spouse/Child)
Health care and dependent care Flexible Spending Accounts
Pre-tax commuter and parking benefits
401(k) Savings and Investment Plan with company match
Paid time off: Flexible Vacation is provided to all eligible employees assigned to a salaried (non-overtime eligible) position. Accrued Vacation is provided to all other employees eligible for vacation benefits. For employees working at least 35 hours per week, the vacation accrual rate is 13 days annually for the first three years of employment and 18 days annually for subsequent years of employment. Vacation accrual is prorated for employees working between 20 and 34 hours per week. Employees working fewer than 20 hours per week are not eligible for vacation.
11 paid holidays
Paid sick leave: 72 hours of paid sick leave upon date of hire. Refreshes each calendar year. Unused balance will carry over each year up to a maximum cap of 112 hours.
Paid parental leave
Adoption assistance
Employee Stock Purchase Plan
Financial planning and group legal
Voluntary benefits including auto, homeowner and pet insurance
The role will generally accept applications for at least three calendar days from the posting date or as long as the job remains posted.
Career Level - IC3
About Us
Only Oracle brings together the data, infrastructure, applications, and expertise to power everything from industry innovations to life-saving care. And with AI embedded across our products and services, we help customers turn that promise into a better future for all. Discover your potential at a company leading the way in AI and cloud solutions that impact billions of lives.
True innovation starts when everyone is empowered to contribute. That’s why we’re committed to growing a workforce that promotes opportunities for all with competitive benefits that support our people with flexible medical, life insurance, and retirement options. We also encourage employees to give back to their communities through our volunteer programs.
We’re committed to including people with disabilities at all stages of the employment process. If you require accessibility assistance or accommodation for a disability at any point, let us know by emailing View email address on click.appcast.io or by calling View phone number on click.appcast.io in the United States.
Oracle is an Equal Employment Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability and protected veterans’ status, or any other characteristic protected by law. Oracle will consider for employment qualified applicants with arrest and conviction records pursuant to applicable law.
- The Senior Regulatory Affairs Specialist provides hands‑on regulatory affairs support for new product marketing... ...for scientific validity and compliance to regulatory standards and provide... ...Affairs, preferably in the medical device industry. FDA, EU, Health Canada,...SeniorMedical device
- ...supports the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges. With a global... ...regulations and guidance as they pertain to compliance; maintains knowledge relating to...SeniorMedical deviceRemote jobWorldwide
- NCBiotech is seeking a Senior Regulatory Affairs Specialist to provide hands-on support for marketing approvals and renewals. The role involves authoring regulatory submissions, maintaining compliance documents, and representing Regulatory during audits. The ideal candidate...SeniorMedical device
$44 - $60 per hour
Job Title: Consultant, Regulatory Affairs Specialist, Medical Device Duration: This will be a 6‑month contract to hire opportunity, with an onsite requirement... ...Affairs team, you will support both regulatory compliance and submission activities, contributing across a...Medical deviceContract workWorldwideRelocation$61.81k - $84.99k
..., reporting, recordkeeping, audits, and internal compliance processes related to DEA and other regulatory agency requirements. The position partners cross-... ...tracking distribution of prescription drugs and medical devices. Conduct periodic audits on facilities and customer...Medical deviceWork experience placementWork at officeLocal areaWorldwideFlexible hours$117.77k - $161.93k
...Management Quality Professional to effectively manage supplier compliance. This role involves implementing supplier requirements,... ...Sciences or a technical discipline with 5-7 years' experience in medical devices or related industries. Benefits include medical, dental,...SeniorMedical device- ...A leading medical technology firm is seeking a Senior Advisor, Regulatory and Clinical Affairs to oversee regulatory strategies and support FDA submissions for innovative medical devices. The ideal candidate holds a Master's degree with a strong clinical foundation and...SeniorMedical deviceRemote work
- ...anticipation of future opportunities within our Regulatory team. Candidates may be considered for... ...globally. As a Regulatory Intelligence Senior Consultant, you will serve as a key... ...development decisions and sustained regulatory compliance. In this consultative role, you will...SeniorLocal areaImmediate startRemote work
$35.98k - $50k
Food Regulatory Specialist I Agency: N.C. Department of Agriculture and Consumer Services Division: Food & Drug Protection Division - Agriculture... ...that foods, drugs, livestock feeds, fertilizers, and medical devices are wholesome and properly labeled through thorough...Medical deviceCasual workRelocationNight shift- ...countries and regions. Summary Plasma Regulatory Affairs oversees the licensing,... ...licensure and registration (biologics (BLA), medical device), Health Canada licensing, Clinical... ...administrative activities for existing licenses in compliance with US FDA, CLIA, PPTA and COLA...Medical deviceWork at office
$111k - $165k
Overview The Senior AML/CFT Compliance Officer is a senior individual contributor role responsible for ensuring the effectiveness and continuous... ...the risk of cryptocurrency banking that align with regulatory requirements and industry best practices. Responsibilities...SeniorRemote job- A leading medical device company in Raleigh is seeking a Sr. Quality Systems Engineer - CAPA. This role involves managing the CAPA process to ensure compliance with regulatory requirements and enhance product quality. The ideal candidate will have at least 8 years of experience...SeniorMedical device
$183k - $228.8k
...across Industrial Quality & Research, Medical Technology, Consumer Markets and Semiconductor... ...role. Role What\'s the role? The Senior Advisor, Regulatory and Clinical Affairs, US is... ...approvals (PMAs) and investigational device exemptions (IDEs). In addition, they are...SeniorMedical deviceLocal areaRemote work- ...as we continue to #discoverbetter. What is the role? The Senior Manager, Regulatory Affairs will develop and execute submission delivery... ...years in Regulatory Affairs within pharma, biotech, or medical devices. Strong project management skills with the ability to manage...SeniorMedical deviceWork at office3 days per week
- ...capabilities built in such as security, compliance controls, and observability. For more information, visit EDB is seeking a Senior Partner Account Executive for our USA... ...Understanding how these technologies apply to medical devices, health records, and utility...SeniorMedical deviceRemote work
- ...A leading healthcare company is seeking a Senior Product Manager to manage the Interventional GI & Accessories team. This role involves... ...candidate will have over 10 years in marketing and strong medical device experience. The position offers an opportunity for innovation...SeniorMedical deviceRemote work
- ...A leading medical device firm is seeking a Senior Product Manager/Product Manager to enhance patient care through innovative medical technology. The role involves strategic management of products, conducting market research, and collaborating with cross-functional teams...SeniorMedical deviceRemote work
$99.3k - $198.7k
...Candidates should have a Bachelor's degree and 3-5 years of experience in enterprise account sales, preferably in the Diagnostics or Medical Device industry. This remote position requires up to 70% travel, with a competitive salary range of $99,300 to $198,700 depending on...SeniorMedical deviceRemote job$126k - $178k
...lasting relationships with medical professionals and... ...transform patient care with devices supported by clinical... ...objective of the Senior Product Manager, Field... ...clinical evidence, FDA regulatory approvals, and market... ...digital platforms; ensure compliance, documentation, and...SeniorMedical deviceWork experience placementWork at officeNight shift$110.2k - $151.5k
A leading medical device company in the United States is seeking a Senior Customs Specialist. This role involves executing customs operations and ensuring compliance with regulations in a highly regulated environment. Candidates should have over 7 years of experience in...SeniorMedical deviceFull time- A leading medical device company in Raleigh is looking for an Embedded Qt Studio Software Architect to enhance their infusion pump platform. This role involves innovative software design, cross-functional team collaboration, and mentorship of junior engineers. The candidate...SeniorMedical device
- ...The Senior Market and Business Development Manager (MBD) will support the Directors of Business Development in selling Cytel's clinical... ...connections at director levels and above in biopharmaceutical/medical device industries a plus. Experience creating positive meeting...SeniorMedical device
- ...Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in Laboratory, Compliance, Computer, Engineering, Project Management, Validation... ...ethics standards for the following position: Sr. Regulatory Affairs Manager Summary: The Sr. Regulatory Affairs...SeniorMedical device
$128k - $176k
...across digital applications. The ideal candidate will have extensive experience in product management, especially within regulated medical device environments, and strong collaboration skills. Competitive compensation and benefits are offered, including a salary range of $...SeniorMedical device$126k - $178k
A leading medical device company is seeking a Senior Product Manager in Raleigh, North Carolina, to lead hospital optimization initiatives for Transcatheter Heart Valve programs. This role involves program leadership, stakeholder engagement, and strategic planning with...SeniorMedical device- ...save for a better today and tomorrow. Job Summary : Performs compliance testing, document support and government forms preparation for... ...including pregnancy, childbirth, breastfeeding and/or related medical conditions), gender, gender identity, gender expression,...SeniorLocal areaRemote work
- ...available in the US and around the world. Regulatory Affairs Consultant, In Silico Modeling... ...highly desirable. Combination Drug and Device regulatory submission experience is a plus... ...of launching a drug, biologic or medical device into multiple markets. The first...Medical deviceLocal areaRemote work10 hours per week
- ...IU- Senior Territory Manager-Raleigh Date: Apr 30, 2026 Location... ...and clinically effective devices that address unmet needs in... ...healthcare providers an array of medical technology solutions that... ...regulations, including strict compliance with applicable policies and...SeniorMedical deviceWork experience placementWork at officeNight shift
- ...managing ongoing projects, fostering Agile practices, and ensuring compliance with regulatory standards. Ideal candidates should have over 10 years of experience in software development for medical devices, along with a relevant degree. Baxter offers support for flexible...SeniorMedical deviceRelocation packageFlexible hours
- ...automotive systems company is seeking a Customs Operations Senior Specialist based in Mount Pleasant, Pennsylvania. The role involves... ...operations related to inbound shipments, ensuring compliance with regulatory requirements. Candidates should have over 10 years of experience...Senior
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Senior Regulatory Compliance Specialist Medical Device. Be the first to apply!
- information security compliance analyst Raleigh, NC
- senior compliance officer Raleigh, NC
- compliance associate Raleigh, NC
- senior regulatory affairs specialist Raleigh, NC
- senior compliance analyst Raleigh, NC
- compliance analyst Raleigh, NC
- cybersecurity policy and compliance analyst Raleigh, NC
- regulatory officer Raleigh, NC
- coding compliance specialist Raleigh, NC
- compliance consultant Raleigh, NC

