Technical Writer- Healthcare Regulatory
Ciel HR View all jobs
- Maharashtra Karnataka
- Contract
- Full-time
- Understand requirements and specifications for the program.
- Develop comprehensive documentation to enhance operational efficiency and regulatory compliance.
- Record and track quality metrics, including bug reports, test cases, and compliance documentation.
- Align documentation with relevant regulatory standards such as HIPAA, GDPR, GCP, GDP, 21 CFR Part 11, etc.
- Ensure accuracy, completeness, and adherence to established standards.
- Incorporate feedback and updates from the quality assurance team.
- Manage versioning and access control effectively.
- Postgraduate/Graduate degree in Life Science.
- Firm understanding of the Systems Development Lifecycle (SDLC).
- Previous experience as a Technical Writer or Quality Assurance Specialist in medical device software or healthcare applications.
- Strong understanding of quality management principles, including standards such as GCP and GDP.
- Deep knowledge of evolving regulatory guidelines (FDA, EMA, GDPR, 21 CFR Part 11, GXP, etc.).
- Understanding of compliance frameworks and their application to data management.
- Knowledge of quality assurance principles and practices.
- Proven experience as a Business Analyst in regulatory management.
- Ability to write user-friendly, engaging content about technical subjects.
- Skill in translating technical information for a general audience.
- Familiarity with content and learning management systems (CMS and LMS).