CQV Engineer: Lead Equipment IQ/OQ/PQ & Commissioning

A life sciences consultancy in France is seeking a professional with 2-3 years of technical experience in Commissioning, Qualification, and Validation (CQV). You will work closely with engineering teams, develop detailed commissioning plans, and conduct thorough checks on systems. Strong knowledge of FDA and GMP regulations is required, along with excellent problem-solving skills and proficiency in English. This role is pivotal in ensuring equipment compliance and functionality.

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