Associate Director, Labeling & Technical Writer

BD

San Diego, CA, USA
Base: $137,100.00 - $226,300.00 usd annual; bonus/...
Fully remote
Technical writing for medical devices
Regulatory compliance documentation
People leadership and team management
The Associate Director, Senior Technical Writer is a strategic documentation leader responsible for driving the development, quality, and evolution of technical documentation for Class II medical devices

Job Summary

  • The Associate Director, Senior Technical Writer is a strategic documentation leader responsible for driving the development, quality, and evolution of technical documentation for Class II medical devices.
  • At BD, you’ll discover a culture in which you can learn, grow, and thrive and find satisfaction in doing your part to make the world a better place.
  • BD is one of the largest global medical technology companies in the world, advancing the world of health™ by fostering creativity, innovation, and effective problem-solving.

Matching Summary

The Associate Director, Senior Technical Writer is a strategic documentation leader responsible for driving the development, quality, and evolution of technical documentation for Class II medical devices.

Salary

Base: $137,100.00 - $226,300.00 USD Annual; Bonus/Equity: Not specified; Benefits: Competitive compensation and benefits programs

Skills & Requirements

Must-have

  • Technical writing for medical devices
  • Regulatory compliance documentation
  • People leadership and team management
  • Cross-functional collaboration
  • Documentation lifecycle management
  • Version control and change management
  • Experience with DTP and editing tools

Nice-to-have

  • Knowledge of Agile methodologies
  • Experience with global regulatory submissions
  • Photography and image editing skills
  • Strong communication and problem-solving
  • Familiarity with ERP systems
  • Ability to influence senior stakeholders
  • Culture of continuous improvement

Key Requirements

  • Bachelor’s degree in Technical Communication or related field
  • 7+ years technical writing experience
  • 5+ years in regulated industry experience
  • 3+ years people leadership experience
  • Extensive regulatory compliance knowledge
  • Experience with medical device labeling and packaging
  • Proficiency with version control systems

Work Rights

Not specified

Tailored Resume

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