Patient Relations Decedent Affairs Specialist - San Francisco

The Regulatory Affairs Specialist will support regulatory compliance activities by preparing and executing submissions to FDA and other global regulatory agencies. · ...

+This isn't your typical regulatory affairs position. You'll be teaching AI systems how to think like a regulatory professional. · ...

We're transforming how regulatory documents get written in pharma biotech and medtech through fundamental AI research. · The Role · You'll be teaching AI systems how to think like a regulatory professional evaluating AI-generated content identifying gaps in logic or compliance de ...

Job Summary: · A regulatory representative acts on core product development teams communicating regulatory requirements and impact of regulations to project teams. They provide input related to FDA and international product registrations and licensing requirements. · Maintains an ...

Ensures regulatory compliance by completing thorough assessments and completing the appropriate submissions pertaining to product clearances/approvals by FDA, Notified Bodies, and other regulatory bodies. · ...

Ensures regulatory compliance by completing thorough assessments · and completing the appropriate submissions pertaining to product clearances/approvals by FDA, · Notified Bodies, and other regulatory bodies. ...

+Job Summary · Involves providing a bridge between medical centers and patients / families.++4 years of relevant experience in the fields of Patient Relations and/or Decedent Affairs, or adjacent · Thorough knowledge of Patient Relations techniques and procedures. · ...

Involves providing a bridge between medical centers and patients / families. · Coordinates review of, and response to, complaints and grievances under strict timeframes. · Serves as a liaison between patients/families and medical staff. · ...

We are looking for a Regulatory Affairs Specialist to join our team.The Regulatory Specialist supports the preparation, organization, · and maintenance of regulatory documentation required for the development, · manufacturing, and licensure of vaccines. · Assist in compiling, · f ...

Vaxart is a clinical-stage biotechnology company developing oral recombinant vaccines based on its proprietary delivery platform. · Assist in compiling regulatory submissions. · Maintain document control and archive management. · ...

+Vaxart es una empresa de biotecnología que desarrolla vacunas orales. · Se busca un especialista en asuntos regulatorios para apoyar la preparación y organización de documentación regulatoria para el desarrollo, · fabricación y registro de vacunas. · +Asistir a la compilación, · ...

We're a global healthcare leader that helps people live more fully at all stages of life. · This Senior Regulatory Affairs Specialist will work out of our Alameda, CA location in the Diabetes Care Division. · ...

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 ...

We are seeking a Regulatory Affairs Specialist for a 6-month temporary contract to support regulatory activities for medical devices. · Contribute to the preparation and support of regulatory submissions and filings for U.S. FDA and other global regulatory bodies. · Assess and do ...

This Senior Regulatory Affairs Specialist will work out of our Alameda, CA location in the Diabetes Care Division. · We're focused on helping people with diabetes manage their health with life-changing products that provide accurate data to drive better-informed decisions. · Revi ...

+Job summary · The Regulatory Affairs Specialist supports global regulatory activities for a diagnostic product portfolio under the guidance of senior regulatory staff. · +Foundational understanding of regulatory requirements for medical devices or diagnostics. · Familiarity with ...

+ Work as Senior Specialist Regulatory Affairs at Abbott in Alameda US for $90k - $180k per year. · Abbott is a global healthcare leader helping people live more fully at all stages of life. · This role provides regulatory input on design and development activities for cross-func ...

As a Regulatory Affairs Specialist at Sugar Bowl Bakery (SBB), you oversee regulatory compliance for all products in accordance with local national and international regulations and customer requirements. · ...

The Regulatory Affairs Specialist supports global regulatory activities for a diagnostic product portfolio under the guidance of senior regulatory staff. · This role assists with preparing and maintaining regulatory documentation, · supporting product registrations and post‑marke ...

Job summary · As a Regulatory Affairs Specialist at Sugar Bowl Bakery (SBB), you oversee regulatory compliance for all products in accordance with local, national and international regulations. ResponsibilitiesEnsure compliance with FDA regulationsReview and approve product label ...