Technical writing and root cause analysis define this Operations Technical Writer role at Teva, supporting manufacturing in a GMP-regulated pharmaceutical setting.

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 environment
- 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.

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