Regulatory Affairs Specialist - Santa Clara

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 ...

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 ...

+ 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 ...

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 ...

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

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... · ...

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. · ...

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 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 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. · ...

Regulatory Affairs Specialist at IQVIA prepares regulatory submissions documents to support clinical trial and marketing authorization activities. · ...

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. · ...

+ Job Overview · 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. · +Bachelor's Degree in Lifescience or related discipline. · At least ...

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... · ...

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 ...