Regulatory Affairs Specialist - San Jose

The Regulatory Affairs Specialist is a key partner to R&D, Quality, Manufacturing, and Marketing teams, · responsible for driving regulatory strategy and ensuring compliance with global medical device regulations. · Develop regulatory strategies for new product introductions and ...

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

The Regulatory Affairs Specialist is a key partner to R&D, Quality, Manufacturing, and Marketing teams, responsible for driving regulatory strategy and ensuring compliance with global medical device regulations. · ...

The Regulatory Affairs Specialist prepares and documents regulatory submissions to government agencies. They work on problems of diverse scope where analysis of situations or data requires a review of identifiable factors. · ...

Under general supervision Prepares and/or reviews regulatory submissions documents to support clinical trial and marketing authorization activities for either internal and/or external clients Provides regulatory support for assigned projects. · ...

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. · ...

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 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. ...

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 ...

+ 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 plays a key part in bringing life-changing medical technologies to patients worldwide by ensuring global product registrations move efficiently and compliantly. · Bachelor's degree in Engineering, Science, or related field. · 0+ years of experience in regulatory affairs ...

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 ...

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... · ...

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

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

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. · ...

This Senior Regulatory Affairs Specialist position is an on-site opportunity working out of our Santa Clara, or Temecula, CA locations in the Abbott Vascular Division.Bachelor's Degree in a related field OR an equivalent combination of education and work experience3-4 years of ex ...

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 ...

We are seeking a Principal Regulatory Affairs Specialist to join Abbott's Vascular Division on-site in Santa Clara, CA. As an individual contributor, the Principal Regulatory Affairs Specialist is responsible for providing regulatory guidance to cross-functional partners... · ...