Pharmaceutical Validation Specialist at LAPORTE

Join LAPORTE as a Pharmaceutical Validation Specialist in Greater Edmonton. Your expertise in equipment validation and compliance will be essential for ensuring operational success.
With over 25 years of experience, LAPORTE is seeking a specialist with at least five years in pharmaceutical validation. Your role will include drafting validation documents, executing protocols, and maintaining compliance with Good Manufacturing Practices (GMP). We offer a collaborative and flexible work environment that supports your career growth.
Key Responsibilities:
• Draft and manage master validation documents
• Execute IQ/OQ/PQ protocols for equipment
• Ensure adherence to GMP during all operations
• Collaborate with clients on change management
• Manage and nurture client accounts
Requirements:
• Degree in science, engineering, or related field
• 5+ years in the pharmaceutical sector
• Strong understanding of GMP
• Knowledge of pharmaceutical manufacturing proce...

Ready to Apply?

Submit your application today and join our talented team at LAPORTE.

Submit Application