Senior Validation Engineer
Job Description & How to Apply Below
Lead pharmaceutical validation efforts with LAPORTE as a Senior Validation Engineer based in Greater Edmonton. Bring over 5 years of experience to ensure compliance and enhance manufacturing quality.
As a Senior Pharmaceutical Validation Engineer at LAPORTE, you will oversee critical validation tasks that ensure efficient processes. This position requires drafting master validation documents, executing protocols, and collaborating with client QA teams.
Your role will be pivotal in maintaining compliance with GMP regulations throughout all validation activities.
Key Responsibilities:
• Draft master validation documents for ongoing projects
• Execute qualification protocols for equipment and systems
• Maintain compliance with GMP throughout the validation process
• Provide reports to support clients’ QA teams
• Manage and nurture client accounts for success
Requirements:
• Bachelor’s or master’s degree in a related field
• 5+ years of experience in the pharmaceutical industry
• In-depth knowledge of GMP standards
• Understanding of manufacturing processes
• Availability for travel to client locations
Drive validation success and enhance pharmaceutical processes at LAPORTE with your extensive experience.
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Position Requirements
10+ Years
work experience
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