Seize an opportunity as a Validation Expert for IT Systems at Neopharm Labs. This position is key in ensuring compliance through technical validation of laboratory systems.

Neopharm Labs is seeking a skilled IT Validation Specialist with a solid background in validating computerized systems. With over 30 years of experience, you will play a vital role in developing validation plans and executing compliance strategies that align with regulatory standards. Collaborate with cross-functional teams to deliver high-quality outcomes.

Key Responsibilities:
• Plan and maintain validation for computerized systems
• Author and develop validation protocols and plans
• Approve and review project deliverables including risk assessments




• Document and address validation deviations appropriately
• Prepare detailed reports summarizing validation results

Requirements:
• At least 5 years in pharmaceuticals or medical devices
• 3+ years of experience in Computer System Validation
• In-depth knowledge of GxP standards and GMP principles
• Relevant university degree required
• Proficient in both English and French

Bring your technical skills and regulatory knowledge to actively participate in advancing the life sciences industry with Neopharm Labs.
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📌 Validation Expert for IT Systems (Quebec City)
🏢 gexel tÉlÉcom international
📍 Quebec City