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
Valuable English verbal and written communication skills
Strong 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.