Technical Writer - IV

Techlink Systems Inc.; Saint Paul (MN); On-site; USD 70,000 - 100,000; Full time

Job summary

Techlink Systems Inc. is seeking a Technical Writer for on-site in St. Paul, MN.

The role focuses on researching, writing, and editing technical documentation for new and sustaining products, while collaborating with cross-functional teams to collect inputs for IFUs and ensuring compliance with regulatory labeling requirements. The ideal candidate has 2–6 years of end-user technical writing experience in the medical device or high-tech space, plus experience with content management systems and

Qualifications

• Bachelor's degree in a relevant technical discipline (e.g., engineering, sciences, English) or equivalent.
• 2–6+ years as a technical writer in medical device/high-tech environments.

Responsibilities

• Research, write, edit technical documentation for new and sustaining product development projects.
• Collaborate with engineering, marketing, regulatory, and clinical teams to gather inputs for IFUs.
• Follow internal processes and procedures.
• Understand and comply with medical device regulatory requirements related to labeling.
• Experience releasing documentation in a Document Control system.

Skills

Attention to detail

Self-starter

Content management

Project coordination

Team collaboration

Education

Bachelor’s Degree

Tools

Document Control System

Content Management System

Job description

Job Title: Technical Writer - IV
Location (On-site, Remote, or Hybrid?): St. Paul, MN (onsite)
Contract Duration: Contract until 05/28/2027
Work Hours: TBD Daytime Hours=40 per week

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