AtomVie Global Radiopharma Inc. in Hamilton, ON, is seeking a Scientific and Technical Writer, Process Development.
This advanced role embeds within the Process Development team to author, review, and manage GMP documentation across development, validation, and clinical supply programs. You will work cross-functionally with chemists, operators, and external stakeholders, ensuring high-quality, regulatory-compliant documentation and timely delivery while adhering to Health Canada, FDA, and EU GMP
#J-18808-Ljbffr
📌 Sr. Scientific & Technical Writer, Process Dev (GMP) (Hamilton)
🏢 Socket.dev
📍 Hamilton
Reply to this offer
Impress this employer describing Your skills and abilities, fill out the form below and leave Your personal touch in the presentation letter.