Senior Engineer in Pharmaceutical Validation

Location: Brossard

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 Good 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

• Strong 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 professional growth in Calgary.
#J-18808-Ljbffr