IT Validation Specialist

Neopharm Labs has been a pivotal player in the development of health products for over 30 years, offering analytical services to pharmaceutical, natural health product, and cosmetic manufacturers. The company is committed to industry best practices and compliance with national and international regulations.

As the IT Validation Specialist, you will report to the Metrology Supervisor and be responsible for validating laboratory systems by creating and implementing protocols, data integrity procedures, and master plans for validation projects.

Key Responsibilities

• Plan, execute, and maintain the validation of GxP-impacting computerized systems, including hardware and software.
• Develop and author validation plans and protocols (VMP, VP, IQ/OQ/PQ).
• Review and approve validation deliverables, including URS, FRS, risk assessments, protocols, and validation reports.
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