Now Hiring: Senior Technical writer

Role Description This is a full-time, hybrid role for a Senior Technical Writer. The Senior Technical Writer will be responsible for authoring and maintaining technical documents, such as user manuals, standard operating procedures (SOPs), system guides, quality documents, and other relevant documentation. Additional responsibilities include translating complex technical information into clear and concise content targeted to various audiences, collaborating with engineering and operational teams, and ensuring all documentation adheres to industry standards and regulatory compliance requirements.

** No C2C for this role accepted, Direct hires only

Qualifications

• 10+ years of Experience in pharmaceutical, biotech, or life sciences industries is highly desirable.
• Author and refine SOPs, Work Instructions, and technical documentation to maintain operational excellence and GxP compliance.
• Lead quality-driven workflows, including the creation and execution of Change Controls and the monitoring of CAPAs.
• Proficiency in Technical Writing, Technical Documentation, and Technical Communication.
• Strong attention to detail and the ability to simplify complex technical information.
• Understanding of GxP compliance, regulatory standards, and life sciences or biotech terminology.
• Excellent communication and collaboration skills to work with cross-functional teams.
• Create and revise Quality and Compliance documents such as manufacturing invetigations.
• Must have hands-on experience like working in manufacturing, oeprations or validation groups in large biopharma facilities.
• Bachelor’s degree in Technical Writing, English, Science, Engineering, or a related field.
• Proficiency with documentation tools, such as Microsoft Word, Adobe Acrobat, or other relevant software.
• Travel may be required