Senior Technical Writer, Medical Devices & Regulatory

Medtronic plc; Mounds View, Lafayette, North Haven (MN, CO, CT); On-site; USD 85,000 - 127,000; Full time

Benefits offered by this job

Health, dental, and vision insurance

401(k) with employer match

Tuition assistance/reimbursement

Paid time off

Job summary

Medtronic is seeking a Senior Technical Writer to develop complex medical device documentation for Neuromodulation products. The role involves planning and producing manuals, IFUs, and web-based materials for global markets, ensuring compliance with quality and regulatory standards.

You will interview users and engineers, translate technical data into clear content, and coordinate translations across languages while maintaining high-quality documentation under tight timelines.

Qualifications

• Bachelor’s degree required.
• 4+ years of technical writing experience preferred.
• Experience writing medical/technical documentation for clinicians and patients is desirable.
• Familiarity with medical terminology and regulatory requirements is a plus.

Responsibilities

• Plan, write, and coordinate the timely development of product documentation (instructions for use, user manuals, etc.) for global markets.
• Produce instructions for use, manuals, and other product documentation that meet quality standards.
• Collaborate with international teams to satisfy legal and regulatory requirements.

Skills

Technical writing

Medical terminology

Strong communication

Editing & proofreading

Education

Bachelor’s degree in a relevant field

Tools

MS Word

FrameMaker

Adobe Acrobat

Single-source publishing

Job description

Medtronic is seeking a Senior Technical Writer to develop complex medical device documentation for Neuromodulation products. The role involves planning and producing manuals, IFUs, and web-based materials for global markets, ensuring compliance with quality and regulatory standards.

You will interview users and engineers, translate technical data into clear content, and coordinate translations across languages while maintaining high-quality documentation under tight timelines.