Technician I Staging - Supply Chain

About the role

The Technician I Staging - Supply Chain position supports department functions as a key member. This is an entry level non-laboratory role that allows you to acquire skills working in a cGMP environment.

Responsibilities

• Using FEFO (First Expiry First Out) basis, pick, stock, verify, identify inventory, or deliver materials
• Execute and properly document cGMP biomanufacturing activities and support SOP and Job Aid (JA) completion
• Stage raw materials and components for production by using DSI scanner, mobile device and computers to maintain accurate inventory spreadsheets
• Perform housekeeping, equipment cleaning, waste disposal, and adhere to 5S standards
• Manage all work orders which includes printing, timely picking and staging of all materials, issuing materials to and closing work orders upon completion
• Support production and lab materials replenishment
• Complete inventory cycle count activities as requested

Requirements

• High School Diploma or equivalent
• No experience required, but highly preferred to have 1+ years of experience in cold storage material handling, shipping, or material operations environment
• Experience with JD Edwards (ERP), Microsoft Excel, Word, Outlook, and Teams highly preferred
• Prior experience operating warehouse equipment (handheld scanners, forklifts, pallet jacks, etc.) is preferred
• Prior pharmaceutical or food manufacturing/processing, cGMP, GDP, or GLP experience preferred

Qualifications

• Individual must be able to see, hear, read, and write clear English
• Frequent sitting, standing, walking, reading of written documents and use of computer monitor screen, reaching with hands and arms, talking, writing, listening
• Occasional stooping, kneeling, crouching, bending, carrying, grasping
• Frequent lifting and/or moving up to 10 pounds and occasional lifting and/or moving up to 50 pounds
• Must comply with EHS responsibilities

Skills

• Strong organizational and attention to detail skills
• Basic computer literacy (Microsoft Office Suite)
• Warehouse management and inventory control experience
• Ability to follow cGMP guidelines and procedures

Benefits

• Defined career path and annual performance review and feedback process
• Diverse, inclusive culture
• Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives

Pay

Competitive salary commensurate with experience

Schedule

Wednesday– Saturday, 2pm-12am

Location

100% on-site (Madison, WI)

Company Information

Catalent, Inc. is a leading global Contract Development and Manufacturing Organization (CDMO). Located in Madison, WI, this facility features advanced mammalian cell line engineering and biomanufacturing capabilities using single-use systems to support scalable production. This 263,000 sq. ft. Good Manufacturing Practice (GMP) facility offers integrated formulation and analytical services to address complex development challenges in Biologics.