Senior Engineer In Pharmaceutical Validation Mercier
LAPORTE
LAPORTE is seeking a Senior Engineer specializing in Pharmaceutical Validation in Greater Calgary. Are you ready to apply your validation skills in a respected firm dedicated to quality and innovation? This position requires at least five years of hands‑on experience in pharmaceutical validation and qualification. You will ensure compliance with Positive Manufacturing Practices (GMP) and lead pivotal validation activities while drafting essential documents. Collaborate with QA/Compliance teams to initiate necessary compliance steps and enhance overall manufacturing processes.
Key Responsibilities
- Prepare master validation documents and plans
- Conduct qualification protocols (IQ/OQ/PQ) for systems
- Ensure adherence to GMP during validation tasks
- Collaborate with QA teams to address compliance‑related issues
- Supervise and develop client relationships
Requirements
- Bachelor’s or master’s degree in science or engineering
- Minimum 5 years in pharmaceutical manufacturing or consulting
- Robust understanding of GMP principles
- Familiar with pharmaceutical operational processes
- Willingness to travel to client locations
Join LAPORTE and strengthen your pharmaceutical validation skills in a culture that celebrates innovation and skilled growth in Calgary.
#J-18808-LjbffrVacancy posted 1 day ago
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