Technical Writing Supervisor
About The Position
At Boston Scientific, we advance science for life by transforming lives through innovative medical solutions that improve the health of patients around the world. Within our Vascular and Coronary Therapies division, we are dedicated to developing technologies that diagnose and treat cardiovascular disease with precision, safety, and clinical excellence. Our teams collaborate globally, working at the intersection of science, technology, and compassion to bring life-saving therapies to patients who need them most. As the Technical Writing Supervisor, you will play a dual role as both a leader and an individual contributor providing direction, mentorship, and oversight for a group of technical writers while also engaging directly in the development and review of complex technical documentation for Boston Scientific's cardiology products. This role is ideal for a leader who thrives on balancing strategic management with hands-on involvement, ensuring that every deliverable meets internal quality system requirements and complies with all applicable regulations.
Requirements
- Bachelor's degree in Technical Communication, Engineering, Life Sciences, or a related field.
- 5+ years of experience in technical writing within the medical device, pharmaceutical, or another regulated industry.
- 2+ years of experience in a leadership or supervisory role.
- Strong understanding of regulatory and quality system documentation (FDA 21 CFR 820, ISO 13485, ISO 14971, MDR).
- Excellent written and verbal communication skills.
- Proficiency with document management systems (e.g., Windchill, Agile PLM) and Microsoft Office authoring tools.
- Exceptional attention to detail and project management skills.
Nice To Haves
- Experience supporting peripheral or coronary medical device products.
- Experience authoring design history, risk management, and post-market surveillance documentation.
Responsibilities
- Lead, mentor, and develop a team of technical writers by investing in their growth, creating clear development paths, and cultivating a supportive, collaborative environment where individuals can thrive and advance their careers.
- Contribute to the development and cohesion of the broader Technical Writing organization at the Arbor Lakes site, helping to align best practices, share knowledge, and strengthen engagement.
- Oversee the creation and maintenance of product technical documentation, including design history files (DHF), risk management deliverables, and post-market surveillance deliverables.
- Collaborate with R&D, Quality, Regulatory Affairs, and Marketing teams to gather technical content and ensure alignment across functions.
- Manage high-impact documentation projects in a fast-paced environment, including recall- or field action-related deliverables.
- Support regulatory submissions and audits by providing compliant and accurate documentation.
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Industry
Merchant Wholesalers, Durable Goods
Number of Employees
5,001-10,000 employees
