QMS Technical Writer - Medical Devices

Philips Corporation

IN Full–time
Posted on: March 06, 2026
Role Overview: As a QMS Technical Writer in the Medical Devices field at our company, you will support in creating and reviewing user documentation in accordance with defined processes and quality standards. Your responsibilities will vary depending on the project, involving tasks such as developing technical documentation, collaborating with stakeholders, and ensuring documentation meets organizational standards. Your role also includes representing the user documentation discipline in the project and coordinating documentation planning to align with project requirements and deadlines. Key Responsibilities: - Develop, write, and edit technical documentation such as user manuals, accessory inserts, and customer release notes. - Collaborate with stakeholders to understand product and regulatory requirements, gathering necessary information. - Create and maintain documentation that adheres to organizational standards. - Review and update existing documentation to ensure accuracy, clarity, and consistency. - Organize and present technical information in a user-friendly manner. - Work with cross-functional teams to ensure timely delivery of documentation projects. Qualifications Required: - Bachelor's/Master's degree with at least 5+ years of experience in technical writing. - Experience in the Medical Devices industry is preferred. - Knowledge of the Document development life cycle. - Excellent writing, editing, grammar, and verbal communication skills with proficiency in English. - Familiarity with technical writing tools and Content Management Systems like DITA, Adobe Acrobat, and SnagIT. - Knowledge of SAP/Windchill/Configuration management systems is a plus. - Strong team player with the ability to plan, schedule, and be flexible in meeting tight deadlines. - Strong time management skills and the ability to prioritize multiple tasks. Additional Company Details: About Philips: Philips is a health technology company dedicated to ensuring that every human matters and has access to quality healthcare. Our commitment is to improve lives globally through innovative healthcare solutions. Join us in doing meaningful work that impacts the lives of others. If you are interested in this role and possess most, if not all, of the required experiences, we encourage you to apply. Your skills and passion may make you the right candidate for this opportunity at Philips. Learn more about our dedication to diversity and inclusion on our website. Role Overview: As a QMS Technical Writer in the Medical Devices field at our company, you will support in creating and reviewing user documentation in accordance with defined processes and quality standards. Your responsibilities will vary depending on the project, involving tasks such as developing technical documentation, collaborating with stakeholders, and ensuring documentation meets organizational standards. Your role also includes representing the user documentation discipline in the project and coordinating documentation planning to align with project requirements and deadlines. Key Responsibilities: - Develop, write, and edit technical documentation such as user manuals, accessory inserts, and customer release notes. - Collaborate with stakeholders to understand product and regulatory requirements, gathering necessary information. - Create and maintain documentation that adheres to organizational standards. - Review and update existing documentation to ensure accuracy, clarity, and consistency. - Organize and present technical information in a user-friendly manner. - Work with cross-functional teams to ensure timely delivery of documentation projects. Qualifications Required: - Bachelor's/Master's degree with at least 5+ years of experience in technical writing. - Experience in the Medical Devices industry is preferred. - Knowledge of the Document development life cycle. - Excellent writing, editing, grammar, and verbal communication skills with proficiency in English. - Familiarity with technical writing tools and Content Management Systems like DITA, Adobe Acrobat, and SnagIT. - Knowledge of SAP/Windchill/Configuration management systems is a plus. - Strong team player with the ability to plan, schedule, and be flexible in meeting tight deadlines. - Strong time management skills and the ability to prioritize multiple tasks. Additional Company Details: About Philips: Philips is a health technology company dedicated to ensuring that every human matters and has access to quality healthcare. Our commitment is to improve lives globally through innovative healthcare solutions. Join us in doing meaningful work that impacts the lives of others. If you are interested in this role and possess most, if not all, of the required experiences, we encourage you to apply. Your skills and passion may make you the right candidate for this opportunity at Philips. Learn more about our dedication to diversity and inclusion on our website.

About Company

Philips Corporation

https://www.philips.com

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