GMP manufacturing expertise meets pharmaceutical compounding at CPL, with afternoon and midnight shifts available under a 12-month contract.

As a Compounder, you will manufacture non-sterile liquid and semi-solid pharmaceutical products according to Manufacturing Work Orders. The work requires following SOPs, GMPs, GDPs, and labour standards. You will support product quality, efficiency, equipment readiness, and continuous improvement throughout manufacturing activities.

Key Responsibilities:

- Weigh, verify, and compound raw materials for production batches
- Complete manufacturing tags and documents using Right First Time practices
- Clean, sanitize, and reassemble product-contact equipment
- Check equipment calibration and accuracy before use




- Contribute to Lean Goals and continuous improvement initiatives

Requirements:

- Post-secondary education in a related field, or equivalent experience
- One to two years of pharmaceutical or regulated manufacturing experience
- Good English verbal and written communication skills
- Robust attention to detail and mechanical aptitude
- Ability to enter confined spaces and wear a respirator

Apply pharmaceutical manufacturing, GMP documentation, and compounding skills as a CPL Compounder across scheduled production shifts.

📌 Pharmaceutical Compounder GMP Manufacturing (Canada)
🏢 Contract Pharmaceuticals
📍 Canada