A leading Biotech Consultancy firm in Ireland seeks an Engineering Specialist (Validation) to support validation activities in a cGMP regulatory environment. The successful candidate will engage in quality assurance, documentation, and compliance, alongside other responsibilities in a dynamic team setting. Ideal candidates will have technical qualifications in Pharmaceutical or Biological sciences, strong analytical skills, and experience in GMP manufacturing. This role offers opportunities for career growth and development in a diverse cultural work environment.
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