Support the end-to-end product development pipeline for new products, renovations, and reformulations, from research and concept development through technical execution and cross-functional coordination. This role involves gathering and comparing supplier and co-manufacturer quotes, minimum order quantities, lead times, samples, specifications, and costing information to support feasibility decisions. The Associate Manager will coordinate day-to-day development needs with ingredient suppliers and contract manufacturers, including documentation, samples, timelines, technical questions, and follow-up. A key part of the role is partnering with Technical Services, Manufacturing, Operations, Quality, and other teams on bench-top testing, pilot runs, scale-up activities, specifications, validation support, and technology transfer. The position also requires researching emerging ingredients, technologies, dosage forms, delivery systems, competitive products, suppliers, and manufacturing capabilities to help identify product opportunities. Additionally, the role involves reviewing and summarizing clinical research, technical data, ingredient evidence, and supplier materials in partnership with Scientific Affairs, and supporting ingredient evaluation and claims substantiation by organizing relevant scientific and technical information. Maintaining accurate product development records, including formulation information, specifications, raw-material documentation, feasibility records, costing inputs, development summaries, approvals, and pilot and scale-up records is essential. The role also supports international market and offshore development opportunities by coordinating local requirements, supplier and co-manufacturer information, samples, documentation, and project tracking. Finally, the Associate Manager will identify project issues and escalate risks appropriately while keeping development work organized and moving forward.
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Job Type
Full-time
Career Level
Mid Level