Join AtomVie Global Radiopharma as a Technical Writer focused on manufacturing documentation in Hamilton, ON. Your role will be key in documenting processes that impact radiopharmaceutical quality.
As a Technical Writer, you'll work collaboratively within a team to author and manage documents that comply with GMP regulations. This entry level position allows you to engage in continuous improvement projects and enhance the efficiency of manufacturing operations. Your responsibilities include ensuring high-quality document creation while navigating various project activities.
Key Responsibilities:
• Write and revise technical documents and SOPs
• Assist in the completion of QMS documentation
• Coordinate project activities for on-time delivery
• Map processes to identify improvement opportunities
• Support CAPA implementation and follow-ups
Requirements:
• Bachelor’s degree in Chemistry or a related discipline
• 1-3 years of relevant technical writing experience
• Excellent grammar and writing skills
• Proficiency in Microsoft Office
• Understanding of GMP standards
Elevate your writing career by contributing to healthcare innovation at AtomVie.
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📌 Technical Writer Support Role at AtomVie (Mississauga)
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📍 Mississauga