Technical Writer (Life Sciences/Clinical)

Duration: 4 months 100% Remote E.S.T Time Zone (Night-Shift)

Scope: Develop, update, and manage crucial, compliant documentation such as Standard Operating Procedures (SOPs), work instructions, and technical reports. This role often supports engineering, manufacturing, and IT systems, ensuring regulatory compliance and effective knowledge transfer.

Required Skills Documentation Development: Writing, reviewing, and editing, and updating SOPs for manufacturing, QC, and technical operations. Systems & IT Support: Documenting IT systems, software validation, or data integrity procedures related to biotechnology, often involving close collaboration with IT and engineering teams. Regulatory Compliance: Ensuring all documentation aligns with GMP (Good Manufacturing Practices) and regulatory requirements. Technical Content: Creating manuals and guides for technical staff, translating complex technical information into clear, actionable, and user-friendly documentation.