Senior Medical Safety Lead, Diabetes Devices

Minimed

Oregon

Ibrido

USD 87.000 - 149.000

Tempo pieno

8 giorni fa

Una candidatura completa in un minuto

Curriculum e lettera di presentazione personalizzati, pronti da inviare.

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Vantaggi offerti da questo lavoro

Health insurance
Dental & vision
401(k) with match
Paid time off
Wellness programs

Descrizione del lavoro

MiniMed is seeking a Senior Medical Safety Specialist to provide medical safety input across the product life cycle, collaborating with R&D, Quality, Regulatory, and Clinical teams. You will evaluate events, author safety assessments, and help translate findings into regulatory submissions and post-market actions.

The role requires licensed healthcare experience and strong clinical knowledge in diabetes-related safety matters, with a focus on patient safety and data-driven decision making.

Competenze

  • Licensed healthcare professional with clinical knowledge and patient care experience.
  • Strong understanding of medical safety concepts and product life cycle.
  • Ability to synthesize medical information for internal stakeholders.
  • Experience communicating safety information effectively.

Mansioni

  • Evaluate events and safety signals from quality, clinical and regulatory sources.
  • Author safety assessments using literature, registries and data sources.
  • Elevate safety issues for investigation and action with cross-functional partners.
  • Obtain input from external experts on safety matters as needed.
  • Provide medical input for regulatory reports and post-market activities.

Conoscenze

Medical safety input
Safety assessments
Safety inquiries
Medical communication

Formazione

Bachelor's degree with 4+ years clinical experience
Licensed healthcare professional (RN/MD/PA/NP)

Strumenti

Microsoft Word
Microsoft Excel

Descrizione del lavoro

MiniMed is seeking a Senior Medical Safety Specialist to provide medical safety input across the product life cycle, collaborating with R&D, Quality, Regulatory, and Clinical teams. You will evaluate events, author safety assessments, and help translate findings into regulatory submissions and post-market actions.

The role requires licensed healthcare experience and strong clinical knowledge in diabetes-related safety matters, with a focus on patient safety and data-driven decision making.

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