Technical Writing Supervisor

Additional Location(s):  N/A

Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance

At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we’ll help you in advancing your skills and career. Here, you’ll be supported in progressing – whatever your ambitions.           

About the Role

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.

Work Mode:

At Boston Scientific, we value collaboration and synergy. This role follows a hybrid work model requiring employees to be in our Maple Grove, MN office three days per week.

Relocation Assistance:

Relocation assistance is available for this position at this time.

Visa Sponsorship:

Boston Scientific will not offer sponsorship or take over sponsorship of an employment visa for this position at this time.

Key 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.

Qualifications

• 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.

Preferred Qualifications

• Experience supporting peripheral or coronary medical device products.
• Experience authoring design history, risk management, and post-market surveillance documentation.

 

Requisition ID: 617807 

Minimum Salary: $ 63900 

Maximum Salary: $ 121400 

 

The anticipated compensation listed above and the value of core and optional employee benefits offered by Bost