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 processes • Av...