Technical Writer

2 weeks ago

bangalore, India Motherson Health & Medical Full time

Documentation Development:

  • Collaborating with subject matter experts to write product documentation, including user manuals, system guides, repair manuals, field service manuals, etc.
  • Disseminate technical information in easy-to-understand language for non-technical audiences.
  • Create software documentation after a thorough collaboration with subject matter experts.
  • Determine the needs of end users for better technical documentation.


Content Review and Quality Assurance:

  • Continuously improve and update existing technical content, marketing materials, and website to ensure accuracy and completeness of the information.
  • Support in reviewing the technical documentation for regulatory submissions, design documentations, and clinical documents.
  • Conduct proofreading, editing, document formatting, review comment incorporation and document completion / approval activities.


Regulatory and Compliance Support:

  • Participate in the development and review of documentation, for global regulatory submissions, adapting content to meet specific regional requirements.
  • Support technical/clinical/regulatory writing for global regulatory submissions in electronic format, when needed.
  • Ensure all documentation is aligned with regulatory standards, formatted for compliance, and approved by relevant stakeholders.
  • Facilitate communication and exchange of documents between stakeholders (e.g., internal personnel such as Regulatory Affairs, R&D, Clinical, Sales and Marketing, Quality Assurance, as well as external vendors such as CROs, if applicable).


Clinical Evaluation Support:

  • Perform literature searches on various databases.
  • Write and edit, as needed, Clinical Evaluation Plans and Clinical Evaluation Reports, and other clinical CER deliverables.


Minimum requirements:

  • Experience: Minimum of 4 years of experience in technical writing. Medical device industry experience will be preferred.
  • Soft skills: Strong communication skills, effective in a complex, global organization. Ability to work as Individual Contributor and take ownership.
  • Effective interpersonal skills: Ability to work collaboratively with cross-functional teams. Should be able to multi-task, managing multiple project activities and organizational responsibilities effectively. Agile thinker and learner, adaptable to dynamic environments.
  • Technical skills: Excellent technical/scientific writing skills. Good understanding of medical device product development would be an added advantage.
  • Education: Bachelor’s degree in engineering or related field. Advanced degree in engineering or scientific discipline preferred.
  • Languages: Verbal and written fluency in English.

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