Bd

Medical Technology

AssociateDirector,SeniorTechnicalWriter

$170–280k San Diego, California, United States; Irvine, California, United States; Franklin Lakes, New Jersey, United States FULL TIME Remote Friendly
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Director candidates.

The Brief

“Associate Director, Senior Technical Writer at Bd. Skills: Technical writing, People leadership, Documentation strategy. Lead technical writers. Develop technical writers”

Industry & Context.

Medical Technology
Problems you'll solve

Problem-solving skills

What They're Looking For.

Must Have

Bachelor’s degree in Technical Communication, Engineering, or related field, 7+ years technical writing experience, 5+ years regulated industry experience, 3+ years people leadership experience

Nice to Have

Master's degree, Leadership of technical writing teams, Medical device organization experience, Deep regulatory compliance knowledge, Manage cross-functional documentation programs, Manage multiple complex projects, Work independently with minimal supervision, Familiarity with electro-mechanical systems, Familiarity with software applications, Experience with device labeling, Experience with packaging content, Knowledge of engineering change control, Knowledge of Agile methodologies, Experience with ERP systems, Proficiency with version control systems, Skilled in technical editing tools, Proficiency with DTP tools

What You'll Do.

Lead technical writers

Develop technical writers

Mentor technical writers

Provide performance feedback

Provide career development

Build documentation function

Establish clear expectations

Foster quality culture

Foster accountability culture

Foster continuous improvement culture

Oversee resource planning

Oversee workload balancing

Oversee vendor management

Oversee contractor management

Represent documentation function

Influence leadership decisions

Own documentation lifecycle

Embed regulatory requirements

Embed quality requirements

Establish documentation standards

Maintain documentation standards

Enforce documentation standards

Establish best practices

Maintain best practices

Enforce best practices

Establish style guides

Maintain style guides

Drive documentation quality

Conduct editorial review

Improve content clarity

Improve content structure

Improve content usability

Partner with engineering

Partner with quality assurance

Partner with regulatory affairs

Partner with clinical affairs

Partner with medical affairs

Partner with marketing

Partner with customer support

Partner with global business units

Collaborate on IFU specifications

Collaborate on quality documentation

Ensure clinical accuracy

Ensure regulatory accuracy

Serve as documentation authority

Influence project scope

Influence project timelines

Influence risk mitigation strategies

Communicate with stakeholders

Communicate with international partners

Ensure timely delivery

Create technical documents

Edit technical documents

Develop visual content

Develop illustrations

Advise on data visualization

Advise on content usability

Stay current on industry trends

Stay current on regulatory developments

Stay current on communication tools

Stay current on communication methodologies

Manage documentation schedules

Manage documentation dependencies

Manage documentation resource requirements

Manage documentation deliverables

Drive process improvements

Enhance documentation quality

Oversee version control

Oversee change management

Oversee documentation integration

How You'll Work.

Team & Collaboration

Cross-functional teams; Leadership forums; Cross-functional meetings

Communication Scope

Excellent communication; Effective communication; Senior-level communication

Process & Methodology

Program management, Project management, Agile methodologies

Full Job Description

## **We are the people who give possibilities purpose** BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it’s no small feat. It takes the imagination and passion of all of us—from design and engineering to the manufacturing and marketing of our billions of MedTech products per year—to look at the impossible and find transformative solutions that turn dreams into possibilities. # Job Description **Associate Director, Senior Technical Writer** **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. This role combines deep expertise in technical writing with strong people leadership, cross‑functional influence, and operational excellence. The ideal candidate brings extensive regulatory experience, excellent communication skills, and the ability to lead a high‑performing team while collaborating across diverse business functions. Key Responsibilities: **Leadership & Team Management** * Lead, develop, and mentor a team of technical writers, illustrators, and/or documentation specialists; provide coaching, performance feedback, and career development. * Build a high‑performing documentation function by establishing clear expectations, aligning team goals to organizational priorities, and fostering a culture of quality, accountability, and continuous improvement. * Oversee resource planning, workload balancing, and vendor/contractor management as needed. * Represent the documentation function in leadership forums and influence decisions affecting product development, quality, labeling, and regulatory deliverables. **Documentation Strategy & Oversight** * Own the end‑to‑end documentation lifecycle for customer-facing and internal technical content including user manuals, IFUs, installation guides, troubleshooting guides, upgrade/downgr

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