International Regulatory Affairs Specialist - San Jose, CA

In this role, you will be part of the regulatory team responsible for proper oversight of medical device development and market introduction. · You will work closely with Quality, Engineering, Product Management, Marketing, and Sales teams to perform regulatory pre- and post-mark ...

Join a pioneering MedTech company that's transforming cardiac care with innovative solutions. · ...

Join a pioneering MedTech company that's transforming cardiac care with innovative solutions. · ...

Responsible for supporting regulatory compliance activities by preparing, assessing, and executing regulatory submissions to FDA, Notified Bodies, and other global regulatory agencies. · ...

The Regulatory Affairs Specialist supports global regulatory strategy and execution for medical device products ensuring compliance with FDA and international regulations throughout the product lifecycle. · This role partners closely with R&D Quality Manufacturing and Clinical te ...

We are united behind our mission: we believe that minimally invasive care is life-enhancing care. · ...

The Regulatory Affairs Specialist supports global regulatory strategy and execution for medical device products ensuring compliance with FDA and international regulations throughout the product lifecycle. · ...

We are hiring for a Regulatory Affairs Specialist to work on-site at our Santa Clara location.This new team member will combine knowledge of scientific regulatory business issues to enable products including combination products that are developed manufactured or distributed to m ...

We are presently hiring for a Regulatory Affairs Specialist to work on-site at our Santa Clara CA location. Prepares robust regulatory applications to achieve departmental and organizational objectives. ...

+ Work that matters · Grow and learn · Care for yourself and your family · Be your true self+Career development with an international company where you can grow the career you dream of. · Excellent retirement savings plan with high employer contribution. · Tuition reimbursement · ...

This role provides compliance support to the Regulatory Affairs organization by driving preparation of KPI dashboards,promoting quality system integration for acquisitions,new product introductions. · Driving preparation of KPI dashboards,maintaining formal RA management review m ...

Ensures regulatory compliance by completing thorough assessments and submitting appropriate documents to the FDA and other regulatory bodies. · ...

We are searching for an experienced regulatory professional to work within the Companion Diagnostics (CDx) team. · ...

We are searching for an experienced regulatory professional to work within the Companion Diagnostics (CDx) team of Dako North America. · Provide expertise in regulatory affairs leading to the successful regulatory registrations and approvals of Companion Diagnostic products in gl ...

We are hiring for a Regulatory Affairs Specialist to work on-site at our Santa Clara, CA location.As an individual contributor, this new team member will combine knowledge of scientific, regulatory and business issues to enable products... · ...

The Regulatory Affairs Senior Specialist is responsible for serving as the RA lead on product lifecycle management project teams.This is a remote position. · ...

Job summary · Regulatory Affairs Specialist – Vascular at Abbott: Enable products that meet required legislation by combining knowledge of scientific, regulatory and business issues. · ...

The Regulatory Affairs Specialist drives regulatory strategy and ensures compliance with global medical device regulations. · ...

The Regulatory Affairs Senior Specialist is responsible for serving as the RA lead on product lifecycle management project teams. · This role includes completing regulatory reporting assessments for anticipated manufacturing, · facility,product,and packaging changes to global reg ...

We are hiring for a Regulatory Affairs Specialist to work on-site at our Santa Clara, CA location. As an individual contributor, this new team member will combine knowledge of scientific, regulatory and business issues to enable products. · ...