Senior Medical Device Technical Writer Onsite MN

Sedaa Corporation; Saint Paul (MN); Presencial; USD 70 000 - 75 000; Tempo integral

Resumo da oferta

Sedaa Corporation in Saint Paul, MN, is seeking a Technical Writer IV to create and maintain high-quality medical/biotech documentation. This onsite role collaborates with engineering, marketing, regulatory, and clinical teams to produce clinician and patient manuals.

The ideal candidate has a Bachelor's in a relevant field and 2–6 years of end-user technical writing experience in a medical device or pharma setting, with strong attention to detail and proficiency in content management and

Qualificações

• Bachelor's degree in a relevant technical discipline, communications, science or English.
• Minimum 2–6 years of progressively more responsible experience as a technical writer in a medical or high-technology environment.
• Experience working in a content management system required.
• Must have current or recent medical device or pharma industry experience.

Responsabilidades

• Research, write, edit technical documentation to support new and sustaining product development projects.
• Collaborate with development engineering, marketing, regulatory affairs, and clinical, among others, to gather inputs for IFUs.
• Follow internal processes and procedures.
• Understand and comply to medical device regulatory requirements related to labeling.
• Technical aptitude for learning new tools and systems.
• Ability to work in a fast-paced and changing environment.
• Experience / familiarity releasing documentation in Document Control system.
• Very high-level attention to detail.

Conhecimentos

Attention to detail

Self-starter

Project management

Multi-project handling

Formação académica

Bachelor's Degree in a technical discipline, communications, science or English

Ferramentas

Document Control System

Content Management System

Descrição da oferta de emprego

Sedaa Corporation in Saint Paul, MN, is seeking a Technical Writer IV to create and maintain high-quality medical/biotech documentation. This onsite role collaborates with engineering, marketing, regulatory, and clinical teams to produce clinician and patient manuals.

The ideal candidate has a Bachelor's in a relevant field and 2–6 years of end-user technical writing experience in a medical device or pharma setting, with strong attention to detail and proficiency in content management and