Life Science Jobs at Medtronic in Istanbul, Türkiye
If you are searching for impactful life science jobs that combine quality, innovation, and global healthcare impact, this Quality Systems Specialist role at Medtronic in Istanbul, Türkiye offers a powerful career opportunity. Designed for professionals and Jobs for Life Science Graduates, this position supports patient safety, regulatory excellence, and global quality systems.
About the Company
Medtronic is a global healthcare technology leader with more than 95,000 employees worldwide. Driven by its mission to alleviate pain, restore health, and extend life, Medtronic careers span R&D, manufacturing, quality systems, and regulatory innovation—making it a top destination for life science jobs globally.
Job Details
- Job Title: Quality Systems Specialist
- Job Requisition ID: R53941
- Location: Istanbul, Türkiye
- Work Arrangement: Flexible / Hybrid (Onsite minimum 3 days per week)
- Employment Type: Full-time
Role Overview
Medtronic is seeking a Regional Field Corrective Action (FCA) Coordinator to join the Center-Led Post-Market Vigilance team. This role is responsible for the planning, coordination, and execution of Field Corrective Actions (FCAs) within the assigned region, ensuring compliance with regulatory and quality system requirements.
You will serve as the primary liaison between regional field teams, Quality Assurance, Regulatory Affairs, Enterprise Core Quality Services (CQS), and global Operating Unit (OU) Quality leadership—playing a critical role in protecting patient safety and ensuring regulatory compliance.
Key Responsibilities
Field Corrective Action Coordination
- Plan and coordinate regional FCA deployment in alignment with Medtronic procedures and work instructions
- Communicate FCA requirements with regional and local QARA teams, field representatives, and sales and marketing leadership
Documentation & Compliance
- Ensure FCA documentation (Global FCA Plan, Field Safety Notices, Customer Acknowledgement forms) is complete, accurate, and compliant
- Maintain adherence to regulatory, quality, and internal documentation standards
Training & Support
- Provide training and guidance to field staff on FCA procedures and best practices
Audit & Regulatory Support
- Support the Operating Unit and local audit programs
- Provide FCA planning evidence and coordinate competent authority or notified body notifications when required
Continuous Improvement
- Identify process improvement opportunities within FCA workflows
- Collaborate cross-functionally to implement enhancements
Required Qualifications for Life Science Jobs
- Bachelor’s degree in Life Sciences or a related field
Experience
- Minimum 2 years in quality systems or regulatory affairs
- Minimum 2 years of project management experience in a regulated environment
- Experience supporting quality system audits (preferred)
Skills & Competencies
- Fluency in English (written and spoken)
- Strong project management and organizational skills
- Excellent written and verbal communication abilities
- Strong critical thinking and analytical skills
- Ability to work onsite at least three days per week
Benefits & Compensation of Life Science Jobs
- Competitive salary
- Flexible benefits package
- Short-term incentive eligibility under the Medtronic Incentive Plan (MIP)
- Comprehensive resources supporting professional growth and work-life balance
Why Medtronic?
At Medtronic, innovation is driven by purpose. From research labs to manufacturing floors, our teams engineer solutions that improve lives. We value diversity, collaboration, and bold thinking—and we empower our people to make a meaningful impact on global health.
