Regional Regulatory Strategy Lead ACEE/TURMECA

Medtronic; Turkey; Hybrid; TRY 2,017,000 - 3,025,000; Full time

Benefits offered by this job

Medtronic Incentive Plan (MIP)

Job summary

Medtronic is seeking a Strategy and Planning Regulatory Affairs professional to drive pre-market submissions across ACEE & TURMECA regions, including Turkey. The role requires coordinating with regional and global RA teams to ensure compliant timelines and quality documentation.

The ideal candidate will have a scientific/engineering background, 2–3 years in medical device regulatory affairs, knowledge of EU MDRs, and strong project management and communication skills. Some travel may be required.

Qualifications

• Experience in regulatory affairs for medical devices and knowledge of regional submissions.
• Familiar with EU MDRs or global regulatory requirements and documentation.
• Strong communication, collaboration, and ability to adapt to priorities.

Responsibilities

• Coordinate regional submission plans for ACEE & TURMECA along with strategic market teams.
• Collaborate with global RA units to manage prioritization and documentation challenges.
• Represent ACEE & TURMECA in pre-market submission harmonization and process improvements.
• Identify opportunities for cross-regional document sharing and ensure timely deliverables.
• Track milestones, identify risks, and report progress to stakeholders.
• Stay updated on regulatory changes and maintain guidance documents.

Skills

Regulatory affairs

EU MDR regulations

Project management

English communication

Adaptability

Education

Bachelor’s Degree in scientific/ engineering discipline

Tools

Copilot AI features

Job description

Medtronic is seeking a Strategy and Planning Regulatory Affairs professional to drive pre-market submissions across ACEE & TURMECA regions, including Turkey. The role requires coordinating with regional and global RA teams to ensure compliant timelines and quality documentation.

The ideal candidate will have a scientific/engineering background, 2–3 years in medical device regulatory affairs, knowledge of EU MDRs, and strong project management and communication skills. Some travel may be required.