Medical Device Regulatory Affairs Development - Santa Clara

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medic ...

Gilead ofrece un programa de aprendizaje y desarrollo para internos que contribuirán a proyectos significativos. · ...

+We're creating a healthier world for all people. For more than 35 years, we've tackled diseases such as HIV, viral hepatitis and cancer – working relentlessly to develop therapies that help improve lives. · +Create custom innovation solutions using different artificial intellige ...

As a Gilead intern you will contribute to high-impact meaningful projects that will not only further advance our company's mission but will allow you to gain real world experience at one of the most innovative organizations in the world. · ...

· Senior/Executive Medical Director, Medical Affairs and Clinical Development– Allergy/Gastroenterology · Allakos Inc. is a clinical-stage company developing therapeutic antibodies for inhibitory receptors on the surface of immune effector cells involved in allergic, inflammator ...

The Quality Engineer IV will provide compliance and quality system support to the Regulatory Affairs organization.This role focuses on audit preparedness, quality system integration, KPI reporting, and driving continuous improvement initiatives to ensure regulatory compliance acr ...

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 ...

+Job Summary · Fueled by innovation at the intersection of biology and technology, we're developing the next generation of smarter, less invasive, more personalized treatments.Are you passionate about improving and expanding the possibilities of surgery? Ready to join a team that ...

This role will provide compliance support to the Regulatory Affairs organization by driving preparation of KPI dashboards and maintaining a pulse on formal RA management review and internal metricsSupporting quality system integration for acquisitions and new product introduction ...

This role involves building and leading corporate communications for Coherent globally.Primary point of contact for corporate communications. · Create and manage communication strategies for the company. · ...

This is a new role that will build and lead corporate communications for Coherent globally. · The VP, Corporate Communications will work closely with and report to the Chief Legal and Global Affairs Officer to devise and execute communication strategies and manage issues,over ti ...

The Regulatory Affairs Manager is responsible for monitoring regulatory requirements that impact HVAC products within the West Coast region. · ...

· 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 ...

· 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 ...

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 ...

Job Description · We are seeking an experienced Regulatory Affairs leader to oversee regulatory planning and operations for Diagnostics Regulatory Affairs (DRA). This role is ideal for someone highly organized and strategically minded who can drive departmental efficiency and ens ...

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... · ...

Abbott is a global healthcare leader that helps people live more fully at all stages of life. · ...

This Regulatory Affairs Manager position is an on-site opportunity working out of our Santa Clara, CA location in the Abbott Vascular Division. · ...

We operate with a purpose-driven, agile, and collaborative culture, where every team member contributes to advancing solutions that improve patient outcomes. · As the Director of Clinical Affairs at VahatiCor, you will be at the forefront of driving and managing the execution of ...