Join AtomVie Global Radiopharma Inc as a Scientific and Technical Writer focused on Process Development in Hamilton ON. Bring your expertise in technical documentation and GMP compliance to support innovative projects. As an advanced-level documentation specialist, you will work closely with process chemists and manufacturing operators. This role demands your strong scientific judgment and organizational skills to produce high-quality documentation for radiopharmaceutical manufacturing.

Your responsibilities include authoring standard operating procedures (SOPs), managing lifecycle documentation, and ensuring compliance with regulations. Key Responsibilities:

- Author and manage GMP documentation for process development
- Support validation and radiopharmaceutical manufacturing documentation




- Conduct reviews and coordinate with cross-functional teams
- Initiate and manage change controls and CAPAs
- Develop templates to enhance documentation efficiency Requirements:
- Minimum 3 years in pharmaceutical GMP documentation
- Proven experience in scientific writing and technical reports
- Master’s degree in Chemistry or related field
- Solid understanding of GMP regulations and practices
- Excellent communication and time-management skills Leverage your scientific writing skills and technical expertise to ensure high-quality documentation at AtomVie in Hamilton.

📌 Technical Writer for Process Development (Canada)
🏢 AtomVie Global Radiopharma
📍 Canada