Spot the pattern. Treat the cancer.
molecular diagnostics • multiomics • machine learning • biotechnology • cancer screening
201 - 500
💰 $290M Corporate Round on 2022-01
August 13
🇺🇸 United States – Remote
⏳ Contract/Temporary
🟡 Mid-level
🟠 Senior
🔏 Technical Writer
🗽 H1B Visa Sponsor
Spot the pattern. Treat the cancer.
molecular diagnostics • multiomics • machine learning • biotechnology • cancer screening
201 - 500
💰 $290M Corporate Round on 2022-01
• Provide documentation writing expertise to support IVD product development projects for Freenome’s diagnostic programs • Collaborate on project teams with scientists, engineers, and other functional stakeholders to develop technical documentation supporting assay/test development, design verification, and design validation activities • Independently manage document reviews and approvals per established approval process within project schedule • Understand processes from both the perspective of the user and the quality system • Promote document best practices across projects; contribute to document improvement initiatives • Be well versed in scientific terminology and principles to produce complex scientific content • Work efficiently and accurately in quality management systems, adhering to best practices and departmental standards for terminology, content management, and reuse • Coordinate and maintain organized records of all supporting materials, document drafts, and versions • Quickly learn and apply new tools, processes, and standards • Demonstrate adaptability and forward thinking in the face of technological or organizational change • Track to and adhere to regulations, standards and guidance that govern the processes documented within the Operations department umbrella (e.g., 21 CFR 820, ISO 13485, etc.) • Review, understanding, and compliance with the Company’s HIPAA Security policies and procedures
• Bachelor’s degree in chemistry, biochemistry, material science, bioengineering, molecular biology, genetics, or relevant field is required • 5+ years’ experience as a technical writer in relevant industry, (biotech, medical device, scientific equipment) focused on scientific or regulatory writing or the equivalent • Experience writing documentation for IVD product development projects • Experience working on technical submissions to the FDA and/or European Regulatory Agencies • Experience with verification and validation protocols/reports • Demonstrated ability to prioritize multiple projects and assignments simultaneously • Demonstrated ability to work cross-functionally • Demonstrated ability to thrive in fast-paced, highly interdisciplinary environment with rapidly changing priorities
Apply NowJuly 24
51 - 200
Create and maintain technical documentation for cloud services and efficient operations.
🇺🇸 United States – Remote
💰 Series B on 2022-12
⏳ Contract/Temporary
🟡 Mid-level
🟠 Senior
🔏 Technical Writer
August 5, 2023
1001 - 5000
🇺🇸 United States – Remote
💰 $200M Series G on 2021-06
⏳ Contract/Temporary
🟡 Mid-level
🟠 Senior
🔏 Technical Writer
🗽 H1B Visa Sponsor