GMP Deviation & CAPA Specialist

Link-Worldwide in Baja California Sur is seeking a professional to manage deviations and oversee investigations in the manufacturing department. Your responsibilities will include authoring investigations, ensuring closures within set timelines, and developing corrective actions to reinforce quality.

The ideal candidate should possess a Bachelor's degree and have 2-5 years of experience in the pharmaceutical industry, particularly in QA roles. Familiarity with GMP regulations is crucial, as well as fluency in English.