C&Q Specialist for GMP Life Sciences & Validation

A leading technical solutions provider in Puerto Rico seeks a qualified professional to support commissioning and qualification activities. The successful candidate will have a bachelor's or master's degree in Chemical Engineering or a related field, along with at least 2 years of experience in GMP manufacturing. Responsibilities include writing and approving protocols, managing change controls, and facilitating technical knowledge transfer. Strong analytical, problem-solving, and communication skills are essential in this collaborative role. #J-18808-Ljbffr