Technical writing and root cause analysis define this Operations Technical Writer role at Teva, supporting manufacturing in a GMP-regulated pharmaceutical environment.
You will create, revise, and maintain controlled documentation for Teva’s Manufacturing team. The role combines technical writing, investigations, document control, and quality systems. You will translate complex processes into clear instructions while supporting compliance and operational excellence.
Key Responsibilities: Author and revise SOPs, work instructions, and manufacturing documents
Maintain forms, templates, training materials, and equipment manuals
Lead investigations involving deviations, non-conformances, and quality events
Apply 5 Whys, fishbone diagrams, and FMEA
Author reports and support timely CAPA closure
Requirements: College Diploma in Science or related discipline
Minimum one year in a GMP-regulated workplace
Experience authoring and revising controlled documentation
Strong technical writing and editing skills
Knowledge of cGMP and Microsoft Office
Apply technical writing, investigation, and document control expertise to Teva manufacturing documentation and quality events.

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📌 GMP Technical Writer Investigations (Ontario)
🏢 Teva Pharmaceuticals
📍 Ontario