Application Programming Interface (API), Current Good Manufacturing Practice (cGMP), Forklift, GMP (Good Manufacturing Practices), Logistics, Manufacturing, Order Picking/Packing, Pallet Jack, Process Improvement, Product Shipments, Regulations, Requirements Management, SAP, Shipping/Receiving, Time Management, Truck Driver, Warehousing
Job Duration: 12months (1st Shift)
Job Location: Portsmouth, NH
Job Description:
Contributes within team using SAP, Syncade and/or Ship console Systems for receipt, storage, issuance, dispensing and allocations of API and consumable components.
Supports Manufacturing in handling & shipping product domestic and internationally.
Demonstrates organization, time management of primary role requirements for one of the following areas within the Logistics department: (Dispensing/FPA, Receiving, Shipping and/or Warehouse)
Roles and responsibilities:
" Performs SAP transactions required for assigned area (Goods Receipt, Stock Put-away, Order Fulfillment, TO Creation, Material Movement)
" Performs Syncade required tasks for assigned area (Receipt, Movement, Material Adjustments, Scrapping, Inventory).
" Demonstrates solid understanding of assigned procedures & obtains required qualifications.
" Demonstrates an understanding of cGMP s required in the workenvironment.
" Performs Circular Chart required tasks for assigned area (Installation,Review, Daily monitoring).
" Perform Logbook entries/review as required for assigned area.
" Performs safe and compliant operation of Class 1,2,3 & 4 for assignedarea.
" Participate in process improvement initiatives.
" Utilizes DMS and Trackwise for assigned area.
" Perform other duties as they are assigned to support department.
" PIT Equipment: Pallet Jacks, Forklifts, Ride On s, Order Pickers, etc.
" Box Truck Driving.
" Lukapak Receiving & Handling.
" Is a Warehouse Environment with Physical Activity Required.
Education
Degree (required)* High School Diploma or Equivalent
Degree (preferred) BS Field of Study
Responsibility*
Adherence to cGMPs is required at all times during the manufacture of APIs.
All personnel own the quality of what they deliver and are responsible for notifying responsible management in a timely manner of regulatory inspections, serious GMP deficiencies, process deviations, product defects and related actions.