Elevate your career as an Advanced Scientific and Technical Writer with AtomVie Global Radiopharma. Contribute to cutting-edge GMP documentation in a team-oriented environment that enhances patient care.
In this advanced position, you will provide essential technical writing support for the Process Development team, ensuring strict compliance with GMP standards. Key responsibilities involve drafting, reviewing, and managing vital documents across clinical supply programs while collaborating with both internal and external partners.
Key Responsibilities:
• Plan and complete GMP documentation for process development
• Author and manage SOPs, batch records, and reports
• Coordinate document reviews with cross-functional teams




• Support documentation for recent equipment validations
• Mentor colleagues on technical writing best practices
Requirements:
• Master’s degree in Chemistry or related fields
• Minimum 3 years in a GMP pharmaceutical setting
• Expertise in scientific writing and regulatory standards
• Robust communication and organizational skills
• Ability to work independently and in teams
Utilize your scientific expertise to make a significant impact at AtomVie Global Radiopharma.
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📌 Advanced Scientific Writer At Atomvie Hamilton (Canada)
🏢 AtomVie Global Radiopharma
📍 Canada