Bristol Myers Squibb Materials Management Senior Associate in Devens, Massachusetts

At Bristol-Myers Squibb, we believe that together we can make the difference. We want to do this by building professional teams who can create and innovate medicines that benefit doctors and their patients.

Our large-scale biologics manufacturing facility in Devens, Massachusetts, is expanding and there are a number of exciting career opportunities to join Bristol-Myers Squibb, one of the world’s leading Biopharma companies.

We’ve created one of the world’s premier biologics facilities, among the first sites in the industry to have a fully automated, integrated manufacturing control system that enables the plant to run virtually paperless. It is a site that combines biologics development with clinical and commercial manufacturing on a single campus – a true biologics center of excellence for the company where teams are encouraged to closely collaborate. This expansion was designed to support the launch of new medicines by more closely aligning biologics development and manufacturing capabilities. All this goes towards helping create and innovate life-saving medicines that fight serious illnesses.

Summary

The Materials Management Senior Associate will perform materials management activities in the JIT Warehouse(s), including inventory management, receiving or transporting material, kitting, and cycle counting.

Responsibilities

  • Performs material handling activities, including material receipt, storage and transfers, to GMP manufacturing facility and finished product from production to interim storage (cold and frozen storage).

  • Works on routine assignments per written procedures with little or no instruction.

  • Adheres to good manufacturing practices, standard operating procedures and, material sampling instructions.

  • Maintains a safe work environment.

  • Completes GMP forms and/or batch records as required for material receiving, shipping activities.

  • Reviews work throughout the process and at completion, in order to ensure that it has been performed properly.

  • Plans/organizes work to ensure that activities are performed effectively, and to respond to fluctuating workloads.

  • Ability to learn and drive forklift and drive company box truck onsite. (No CDL required).

  • Ability to learn and operate turret truck that raises to heights over 25ft in the air

  • Wears the Proper PPE to handle hazardous materials throughout the site.

  • Ability to lift up to 50lbs.

  • Ability to gown and de-gown per SOP for working in clean rooms.

  • Shift is Friday-Monday, 4/10 shift 0730-1730. Hours and shift schedule are subject to change as dictated by work force plans.

Qualifications

  • Minimum of High School Diploma required, Bachelor’s degree preferred.

  • Minimum of 2 years’ experience working in a GMP environment, with one year JIT warehouse experience

  • Preferred experience in Life Sciences/Biopharmaceuticals

  • Knowledge of raw materials, production processes, quality control, costs, and other techniques for maximizing the effective manufacture and distribution of goods in a GMP environment.

  • Strong communication skills written/verbal

  • Successful experience in managing one’s own time.

  • Ability to learn relevant equipment, policies, procedures, and strategies to promote effective operations for the protection of people, data, and property.

  • Ability to learn standard computer based business systems such as SAP, Syncade, Delta V

  • A valid driver’s license is required.

  • Must have knowledge of the proper use and application of personal protection equipment (PPE).

Equal Opportunity Employer Minorities/Women/Protected Veterans/Disabled