Medtronic seeks a Quality Systems Specialist to oversee quality programs, processes, and regulatory compliance at its Buenos Aires facility.
The role involves managing audits, inspections, and documentation while ensuring adherence to internal and external healthcare standards.
Responsibilities
Oversee development and maintenance of quality programs, systems, and procedures ensuring regulatory compliance
Provide expertise on regulatory policies, governmental requirements, and internal regulations for compliance
Supervise continuous process analyses with operational entities to enforce requirements and meet regulations
Lead audit and inspection preparation, findings resolution, and liaison with auditors and inspectors
Prepare reports and documentation including corrective and preventive actions for stakeholders
Requirements
University degree in pharmaceutical chemistry, bioengineering, or biomedical engineering




Minimum two years experience in internal, external, and regulatory audits with preparation and findings closure
Professional experience in medical device companies
Knowledge of Argentine health sector regulations, particularly ANMAT requirements
Familiarity with ISO *****, GDP, or other applicable quality management systems
Advanced English proficiency for integral team interaction
Distribution, warehouse, logistics, or supply chain quality process experience preferred
Join our Research & Development (R&D;) team and contribute to Physical AI, AIoT, IoT, AI/ML, intelligent sensing, Edge AI, connected
systems,
and emerging technologies through research, experiments, prototypes, and proof-of-concept development.
Research Areas
IoT & ...
#J-*****-Ljbffr

📌 Quality Systems Specialist / Argentina (Buenos Aires)
🏢 Medtronic
📍 Buenos Aires