Boston Scientific
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
Hybrid work model: employees are required 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. Salary
Minimum Salary: $63,900 – Maximum Salary: $121,400. Compensation will vary based on location, experience, and other factors. EEO Statement
Boston Scientific Corporation has been and will continue to be an equal opportunity employer. To ensure full implementation of its equal employment policy, the Company will continue to take steps to assure that recruitment, hiring, assignment, promotion, compensation, and all other personnel decisions are made and administered without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, gender expression, veteran status, age, mental or physical disability, genetic information or any other protected class. COVID‑19 Vaccination Requirement
Certain US‑based positions require proof of COVID‑19 vaccination status. Candidates will be notified during the interview and selection process if the role requires proof of vaccination as a condition of employment. Prohibited Substance Test
This role is safety‑sensitive and candidates will be subject to a prohibited substance test as a requirement. The goal of the prohibited substance testing is to increase workplace safety in compliance with the applicable law.
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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
Hybrid work model: employees are required 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. Salary
Minimum Salary: $63,900 – Maximum Salary: $121,400. Compensation will vary based on location, experience, and other factors. EEO Statement
Boston Scientific Corporation has been and will continue to be an equal opportunity employer. To ensure full implementation of its equal employment policy, the Company will continue to take steps to assure that recruitment, hiring, assignment, promotion, compensation, and all other personnel decisions are made and administered without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, gender expression, veteran status, age, mental or physical disability, genetic information or any other protected class. COVID‑19 Vaccination Requirement
Certain US‑based positions require proof of COVID‑19 vaccination status. Candidates will be notified during the interview and selection process if the role requires proof of vaccination as a condition of employment. Prohibited Substance Test
This role is safety‑sensitive and candidates will be subject to a prohibited substance test as a requirement. The goal of the prohibited substance testing is to increase workplace safety in compliance with the applicable law.
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