Principal Technical Writer - Medical Device Labeling
Are you a skilled technical writer with a passion for the medical device industry? Do you have a strong understanding of labeling requirements and regulations? If so, Boston Scientific is seeking a Principal Technical Writer for our Medical Device Labeling team.In this role, you will be responsible for creating and maintaining labeling content for our innovative medical devices. You will collaborate with cross-functional teams to ensure accuracy, compliance, and consistency across labeling materials. As a subject matter expert, you will also provide guidance and mentorship to other writers on the team.To be successful in this role, you must have a bachelor's degree in a relevant field and a minimum of 5 years of experience in technical writing, preferably in the medical device industry. You must also have a deep understanding of labeling regulations and requirements, and possess excellent communication and project management skills.If you are a detail-oriented and driven individual looking to make a meaningful impact in the medical device industry, we encourage you to apply for this exciting opportunity at Boston Scientific.
- Develop and maintain labeling content for medical devices, including instructions for use, product manuals, and packaging materials
- Collaborate with cross-functional teams to ensure accuracy, consistency, and compliance with applicable regulations and standards
- Serve as a subject matter expert on labeling requirements and regulations, providing guidance and mentorship to other writers on the team
- Conduct thorough research and analysis to stay updated on industry trends and changes in regulations
- Manage multiple projects simultaneously, adhering to project timelines and deadlines
- Communicate effectively with stakeholders and team members to gather necessary information and clarify requirements
- Review and edit labeling materials for accuracy, clarity, and consistency
- Work closely with regulatory and quality teams to ensure all labeling materials meet regulatory requirements
- Participate in product development and design reviews to identify labeling needs and requirements
- Identify and implement process improvements to enhance the efficiency and effectiveness of the labeling process
- Maintain organized and accurate records of all labeling materials and revisions
- Continuously strive to improve the quality and usability of labeling materials for end-users.
Extensive Knowledge Of Medical Device Regulations: The Ideal Candidate For This Role Should Have A Deep Understanding Of The Various Regulations And Standards Related To Medical Device Labeling, Such As Fda 21 Cfr Part 801 And Eu Mdr. This Knowledge Is Essential For Ensuring Compliance And Accuracy In Labeling Materials.
Strong Writing And Editing Skills: As A Principal Technical Writer, This Individual Will Be Responsible For Creating And Reviewing Complex Labeling Documents. They Should Possess Excellent Writing And Editing Skills, With The Ability To Communicate Technical Information Clearly And Concisely.
Experience In Medical Device Industry: Previous Experience In The Medical Device Industry Is A Must For This Role. The Candidate Should Have A Solid Understanding Of Medical Device Product Development, Manufacturing Processes, And Labeling Requirements.
Project Management Skills: This Position Will Require The Candidate To Manage Multiple Labeling Projects Simultaneously. Therefore, They Should Have Strong Project Management Skills, Including The Ability To Prioritize Tasks, Meet Deadlines, And Work Collaboratively With Cross-Functional Teams.
Attention To Detail: The Principal Technical Writer - Medical Device Labeling Will Be Responsible For Ensuring The Accuracy And Consistency Of Labeling Materials. Therefore, They Should Have Excellent Attention To Detail And Be Able To Identify And Correct Errors Or Inconsistencies In Labeling Documents.
Project Management
Editing
Technical Writing
Quality Control
Proofreading
Compliance
Documentation management
Medical Devices
Cross-Functional Collaboration
Regulatory Affairs
Fda Guidelines
Labeling Regulations
Communication
Conflict Resolution
Emotional Intelligence
Leadership
Time management
creativity
Teamwork
Active Listening
Adaptability
Problem-Solving
According to JobzMall, the average salary range for a Principal Technical Writer - Medical Device Labeling in Philadelphia, PA, USA is between $100,000 and $150,000 per year. This can vary depending on factors such as experience, qualifications, and the specific company.
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Boston Scientific Corp. engages in the development, manufacture and marketing of medical devices that are used in interventional medical specialties. Its products and technologies are used to diagnose or treat medical conditions, including heart, digestive, pulmonary, vascular, urological, women's health and chronic pain conditions.
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