/ Accountabilities Conduct focused time studies to support packaging operations. Apply complete knowledge of process improvement strategies and lean techniques (e.g. Method analysis, work combination charts, ergonomics, visual controls, safety, 5S, Kanban, poka yoke) to analyze and improve overall packaging operations. Perform and direct data mining and analyze the results

This individual will manage and oversee Site Services support related tasks, vendor relationships, and managed services for non GMP business related support operations. The role will plan and manage projects, develop and implement documented processes to manage costs, and qualitatively improve the variety of services needed to keep the site operational and support the fac

/ Accountabilities Organize and oversee the activities related to the manufacturing of tablets and capsules to include delivery, in process samples in a defined schedule. Review and compile the documents generated during the production of tablets and capsules such as Batch Manufacturing Record (BMR), PQ protocol. Perform SAP entry during and finish batches product. Make eq

Project Management Lead, R&D Posting Date Apr 19, 2024 Country United States State New York Location Central Islip Req Id 84016 Project Management Lead, R&D Central Islip, NY Works under the supervision of the Director of Project Management. This position is responsible for handling R&D activities under Life Cycle Management, organizing meetings with all right stakeholder

/ Accountabilities Inspect carriers/trailers of inbound and outbound shipments and report to WH Coordinator any discrepancies. Escorts drivers always when in the facility and ensure gowning procedures are followed. Receives and unloads freight, checks for damaged goods, verifies items and quantities received with BOL, Packing List, PO, etc. Moves materials as required for

/ Accountabilities Must be willing to work in a pharmaceutical manufacturing setting. Must be able to know how to operate pharmaceutical production machinery independently and thoroughly complete required documentation (legible writing, accurate reporting, maintain and file, etc.) Execute procedures for manufacturing processes in accordance with batch manufacturing record