Technical Writer

Sedaa Corporation; Saint Paul (MN); Vor Ort; USD 70.000 - 75.000; Vollzeit

Zusammenfassung

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

Qualifikationen

• 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.

Aufgaben

• 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.

Kenntnisse

Attention to detail

Self-starter

Project management

Multi-project handling

Ausbildung

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

Tools

Document Control System

Content Management System

Jobbeschreibung

****ONLY FOR CANDIDATES LOCAL TO Greenwood Boulevard Minnesota : St. Paul , Also willing to relocate ***

JOB ID: Sedaa48856

Title: Technical Writer IV

Location: 100 percent onsite- United States : Minnesota : St. Paul : Lillehei : One Lillehei Plaza

Pay Range - 70k to 75k annually

Days/Hours: Mon - Friday Daytime hours

Selected Candidate will start ASAP after screenings have cleared.

Job Description

• 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.
• Requires a Bachelor's Degree in a relevant technical discipline, Communications, Science, English or equivalent.
• Must have a minimum of two to six plus years of progressively more responsible experience as a technical writer in a medical or high-technology (preferably biotechnology) environment.
• Experience working in a content management system required.
• Must have current or recent medical device or pharma industry experience.
• Must have 2-6 years of experience in the medical device industry.
• Must have end-user technical writing experience; that is, direct experience writing clinician and/or patient manuals.

Top qualities:

• Attention to detail
• Self-starter, manage own projects, no handholding
• Learns tools quickly; content management a plus
• Able to juggle multiple projects at once
• Working with project teams