Technical/Scientific writer, Biologics Manufacturing

**HyperMabs** is a dynamic biopharmaceutical company that specializes in the development of novel biologics. Our strength is identifying and developing drugs with transformative potential. Our approach is centred around the incubation of novel ideas for breakthrough medicines and rapidly achieving clinical validation for the most promising candidates. Our highly qualified team of drug developers and company builders has a track record of advancing complex biologics from discovery through clinical trials. Our R&D facilities are located in the heart of **Montreal, Canada**, and comprise laboratory space for pre-clinical research as well as manufacturing development that bolster our mission to serve patients in need. This is a full-time position that is based in Montreal. **Role:** The **technical/scientific writer** comes in support to biological products process and analytical development, technology transfer and manufacturing review of clinical trial material. The incumbent communicates complex scientific and technical information in a clear, concise, and accurate manner. The technical writer/scientist is responsible to create and organize consistent documentation for internal and external communications. **Main Duties and Responsibilities:** * Participate in protocol and report preparation by performing required write-ups and reference searches * Within a project, organize experimental data into tables or graphical representations, organize high-quality images, perform calculations necessary for data interpretation, including statistical analyses and, draft the introduction, discussion and conclusion sections of reports * Ensure thorough revision of documentations for ensuring data integrity * Within the document control procedural, maintain up-to-date document filing and forms for the department * Participate in GMP documents preparation and revision, e.g.: regulatory section, non-conformity and investigations **Qualifications:** * University degree in a scientific field * **Five years** of experience as technical writer or any related experience * Excellent writing and editing skills * Excellent verbal and written communication skills * Ability to work with subject-matter experts or data banks to gather key information * Ability to analyze and understand scientific data and technical specifications in order to produce clear documentation * Excellent organizational, analytical and time-management skills * Attention to detail, and a strong sense of ownership * Experienced user of office software * Experience or knowledge of Good Manufacturing Practice (GMP) or Good Laboratory Practice (GLP) is an asset * Use of AI tools and vibe coding is an asset * This position involves daily collaboration with suppliers, teams, and partners outside of Québec, which requires the candidate to have a proficient knowledge of English in addition to French. Please send your **CV** and **cover letter** outlining your motivation and relevant experience for th