Sr. Regulatory Affairs Specialist EMEA (Registration & Sustaining activity)

Intuitive; Madrid; Sur place; EUR 90 000 - 130 000; Plein temps

Résumé du poste

Intuitive is seeking a Sr. Regulatory Affairs Specialist EMEA to lead regulatory strategy across Europe, the Middle East, and Africa. You will steer registrations, sustain activities, and collaborate with cross‑functional partners to align regulatory requirements with business goals.

The role demands deep knowledge of global medical device regulations and strong project management expertise to support product launches and ongoing compliance in a fast‑paced environment.

Qualifications

• Bachelor’s or Master’s degree in Engineering, Medical Technology, or related field preferred or considered with relevant experience.
• Proficiency in English with minimum C1 level in writing and speaking.
• 8+ years of regulatory affairs experience in the medical device industry, including EU MDR/ISO 13485 familiarity.

Responsabilités

• Lead regulatory strategy for new markets and product expansions in EMEA.
• Manage registration dossiers, renewals, amendments, and change notifications.
• Provide direction on regulatory requirements and coordinate cross‑functional teams.

Connaissances

Regulatory affairs

English (C1)

Formation

Bachelor’s or Master’s in Engineering/Medical Technology or related field

Description du poste

Sr. Regulatory Affairs Specialist EMEA (Registration & Sustaining activity)

• Full-time
• Shift: Day
• Ways of Working: Set Schedule - This job will be onsite weekly, the percentage of onsite work will be defined by the leader.
• Employee Type: Employee
• Global Job Level (HCM): Professional 4 (11)

At Intuitive, we are united behind our mission: we believe that minimally invasive care is life-enhancing care. Through ingenuity and intelligent technology, we expand the potential of physicians to heal without constraints.

As a pioneer and leading company in the field of robotic-assisted surgery, we strive to foster an inclusive and diverse team, committed to making a difference. For more than 25 years, we have worked with hospitals and care teams around the world to help solve some of healthcare’s hardest challenges and advance what is possible.

Intuitive has been built by the efforts of great people from diverse backgrounds. We believe great ideas can come from anywhere—we strive to foster an inclusive culture built around diversity of thought and mutual respect. We lead with inclusion and empower our team members to do their best work as their most authentic selves.

Passionate people who want to make a difference drive our culture—our team members are grounded in integrity, have a strong capacity to learn, the energy to get things done, and bring diverse, real-world experiences to help us think in new ways. We actively invest in our team members to support their long-term growth so they can continue to advance our mission and achieve their highest potential.

Join a team committed to taking big leaps forward for a global community of healthcare professionals and their patients. Together, let’s advance the world of minimally invasive care.

Primary Function of Position:

The Sr. Regulatory Affairs Specialist EMEA plays an important role within the Regulatory Affairs Department, focusing on providing in-depth regulatory expertise for New Product Development (NPD), market expansion and sustaining operations across Intuitive’s product portfolio. This position requires in-depth understanding of global medical device regulations, enabling strategic project management and execution for EMEA regulatory submissions and compliance activities. The Sr. Regulatory Affairs Specialist EMEA leads projects with cross-functional teams, provides direction on regulatory matters, while contributing to the success of product launches and ongoing operations.

Roles and Responsibilities:

• Lead registration strategy with cross-functional partners for implementation of new markets, product expansion in existing markets, and new product introduction within EMEA (EU/EEA, Middle East, Africa) ensuring compliance with local regulations.
• Assess regulatory impact and develop proactive solutions to mitigate anticipated risks/obstacles for market access and distribution.
• Identify regulatory pathways for products under development or design changes, and work with cross-functional teams to align regulatory requirements with business strategy.
• Manage the preparation, submission, and maintenance of EMEA medical device registration dossiers, ensuring compliance with local regulations, timely regulatory approvals, up-to-date records and strategic grouping of countries when possible.
• Prepare and review regulatory correspondence, Letters of Notification, declarations, certificates, and supporting technical documentation.
• Monitor and perform sustaining activities including renewals, amendments, and change notifications for assigned markets.
• Perform regulatory impact assessments and changes throughout the product lifecycle such as design modifications, labeling updates, software releases, etc.
• Develop and manage comprehensive dashboards and effectively integrate team registration trackers, regulatory databases, and product registration records within software applications.
• Proactively monitor and evaluate changes in medical device regulations and standards for global markets, updating departmental procedures and tools as necessary to maintain compliance.
• Support development of country profiles, process maps, and training material.
• Independently manage responses to regulatory authority inquiries and requests for additional information relevant to team activities.
• Support audits, inspections, and compliance activities (including CAPAs, non-conformances) as needed.
• Provide direction to cross-functional teams, interpreting and translating complex regulatory requirements into effective and actionable strategies.
• Perform other regulatory tasks and projects as assigned, ensuring regulatory compliance across regional markets.

Required Knowledge, Skills, and Experience:

• Bachelor's or Master's degree in Engineering, Medical Technology, or a related field is highly preferred, though practical experience in a similar role will be considered.
• Proficiency in English, with a minimum of C1 level proficiency in both written and spoken forms.
• 8+ years of experience in regulatory affairs within the medical device industry, with experience or exposure in the following areas:
  • Medical device registration lifecycle management, including new registrations, renewals, amendments and change management.
  • Regulatory impact assessments and change notification strategies.
  • Advanced understanding of Global regulatory requirements and standards for Medical Devices relevant to product compliance (e.g., EU MDR 2017/745, ISO 13485, RoHS, etc.).

Intuitive is an Equal Employment Opportunity Employer. We provide equal employment opportunities to all qualified applicants and employees, and prohibit discrimination and harassment of any type, without regard to race, sex, pregnancy, sexual orientation, gender identity, national origin, color, age, religion, protected veteran or disability status, genetic information or any other status protected under federal, state, or local applicable laws.

We will consider for employment qualified applicants with arrest and conviction records in accordance with fair chance laws.

U.S. Export Controls Disclaimer:In accordance with the U.S. Export Administration Regulations (15 CFR §743.13(b)), some roles at Intuitive Surgical may be subject to U.S. export controls for prospective employeeswho are nationals from countries currently on embargo or sanctions status.

Certain information you provide as part of the application will be used for purposes of determining whether Intuitive Surgical will need to (i) obtain an export license from the U.S. Government on your behalf (note: the government’s licensing process can take 3 to 6+ months) or (ii) implement a Technology Control Plan (“TCP”) (note: typically adds 2 weeks to the hiring process).

For any Intuitive role subject to export controls, final offers are contingent upon obtaining an approved export license and/or an executed TCP prior to the prospective employee’sstart date, which may or may not be flexible, and within a timeframe that does not unreasonably impede the hiring need. If applicable, candidates will be notified and instructed on any requirements for these purposes.

This position may be filled at a different job level than listed here depending
business need and/or on the selected candidate’s experience, knowledge and skills.
Compensation will be based primarily on the job level at which the role is filled and the
candidate’s qualifications, consistent with applicable law.