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 robust 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
• Strong 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.
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📌 Technical Writer for Process Development (Ontario)
🏢 AtomVie Global Radiopharma
📍 Ontario