Validation Engineer – GMP, CSV & Process Validation

A consulting firm in pharmaceuticals is seeking a skilled candidate for a pivotal role in Validation and Project Management. The successful applicant will have at least 2 years of experience, along with the ability to effectively communicate in both French and English. Responsibilities include commissioning and qualification of pharma systems and ensuring compliance with GMP regulations. The firm offers flexible hours, career development opportunities, and an engaging work environment in Laval, Quebec.
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