About this role
Scientific and Technical Writer, Process Deve at AtomVie Global Radiopharma Inc.. Location: Hamilton, Ontario, Canada. Role: authoring documents, managing documentation, supporting development Requirements: Master's degree required, 3+ years pharmaceutical GMP documentation experience, strong scientific writing and data-interpretation skills, proficiency with Microsoft Office, knowledge of GMP and compendia, ability to support 7-day operations. Category: Research and Development (R&D) Seniority: Mid Level Tools: Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Microsoft Project Commitment: Full Time Workplace: Onsite Languages: English