Validation & Compliance Specialist — GMP, FDA Audits

A leading clinical consulting firm based in Catalonia seeks a Qualification and Validation Specialist. The ideal candidate will have a solid academic background and at least 3 years of experience in the pharmaceutical or medical device sector. Responsibilities include ensuring compliance with validation processes and providing guidance during audits. This position offers a competitive salary package tailored to individual needs, emphasizing continuous learning and career development opportunities in a supportive environment.
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