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Support all functions of the pharmaceutical supply chain for products throughout their lifecycle. This includes products in process development (pre-commercialization) and process optimization (post-commercialization). Ensure products are developed and manufactured per current regulatory requirements and industry standards (cGMP's, QbD, ICH, etc.). Work cross-functionally to ensure raw materials and components are available and product is manufactured within established timelines. The Engineer II will demonstrate a broad understanding of the manufacturing unit operations, equipment, and supply chain from drug product manufacturing (which includes formulation, filling, and manual inspection) through packaging and how the different departments within the organization interact with each other. The Engineer II will assist with planning and execution of routine technical assignments and demonstrate a firm understanding of relevant pharmaceutical regulations related to cGMP manufacturing.