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. · ...

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 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 · ...

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... · ...

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

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. · ...

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. · Develop regulatory strategies for new product introductions and ...

+ 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 ...

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. · ...

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 united behind our mission: we believe that minimally invasive care is life-enhancing care. Through ingenuity and intelligent technology, we expand the potential of physicians to heal without constraints. · ...

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

This role provides compliance and quality system support to the Regulatory Affairs organization. · Drive preparation and maintenance of key performance indicator dashboards · Support audit preparedness initiatives through risk identification, mitigation planning, and preventive a ...