Regulatory Specialist - Santa Clara

Picarro Inc has an opportunity for CEMS Regulatory Specialist that will assist Environmental Solutions team with continuous emissions monitoring systems regulatory reporting daily quality assurance review. · ...

· Title: Regulatory Specialist · Job Location: Remote · Job Term: Full-time · Travel: < 10% · The Opportunity: · Picarro, Inc. has an opportunity for a CEMS Regulatory Specialist to assist the Industrial Solutions team with regulatory reporting for continuous emissions monitor ...

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 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 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 ...

· Company Description · Pharmaceutical / Biotech · Job Description · SR. REGULATORY AFFAIRS SPECIALIST  · California Santa Clara · EXP 7-10 yrs · DEG Bach · RELO · BONUS · Job Description. · We are searching for an experienced regulatory professional to work within the Companion ...

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

Title: Senior Regulatory Affairs Specialist · Location: Santa Clara, CA · Duration: 9+ Months · Responsibilities · Must have 3-5 years of experiences in Medical Device Regulatory Affairs · Needs to have experience in Regulatory Change Assessment for Class III medical devices and ...

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... · ...

· Company Description · Pharmaceutical / Biotech · Job Description · SR. REGULATORY AFFAIRS SPECIALIST  · Santa Clara, CA  · Pharmaceutical / Biotech · EXP 7-10 yrs · DEG Bach · Relo · Bonus · Job Description · We are searching for an experienced regulatory professional to work ...

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. · ...

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