Support radiopharmaceutical manufacturing documentation at Jubilant Radiopharma using GMP awareness, SAP, and meticulous record review. Help protect documentation accuracy across production activities.
As a Production Documentalist, you will coordinate, review, and manage manufacturing documentation with Production, Quality Control, and Quality teams. Your work supports documentation integrity, valuable documentation practices, compliance, and continuous improvement. The role includes batch records, logbooks, registers, and other GMP-related documents.
Key Responsibilities: Coordinate and distribute documentation after manufacturing batch activities
Print, prepare, verify, and release production documents
Review and approve batch records and GMP documentation




Prepare weekly documentation performance KPI reports
Support document management, archiving, and process improvements
Requirements: Experience in pharmaceutical production
Strong attention to detail and sustained concentration
Manual dexterity for documentation-related activities
Proficiency with Microsoft Word, SAP, and Excel
French and English spoken and written knowledge
Bring pharmaceutical production experience, documentation discipline, and system proficiency to Jubilant Radiopharma’s quality-focused operations.

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📌 Pharmaceutical Production Documentation Specialist (Quebec City)
🏢 Jubilant Radiopharma
📍 Quebec City