A European engineering services company is seeking a CQV Engineer to work on-site in Switzerland. You'll be responsible for executing and approving validation activities, supervising vendors, and ensuring compliance with GMP regulations. The ideal candidate has 3+ years of CQV experience in the pharma/biotech fields and holds a relevant degree. Strong communication skills in German and/or English are required. You'll engage in challenging projects with opportunities for career development within a supportive team culture.
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