Production Chemist

in Indianapolis, IN

Production Chemist Job

Job Description Job Attributes+

  • Job ID

    e3e57d52-add4-4e2b-b1b4-b58948a9088e

  • Req #

    20088414

  • Job Location

    7920 Georgetown Rd.
    Indianapolis, IN 46268, US

  • Job Category

    Manufacturing

  • Job Type

    Regular

  • Schedule

    Full time

The Production Chemist, Nuclear Manufacturing position is part of a growing Technical Operations team within Cardinal Health’s Nuclear and Precision Health Solutions organization tasked with the routine manufacture of sponsor radiopharmaceutical products. This position will be responsible for supporting all activities required to operate a clinical phase manufacturing and testing facility, with strict adherence to cGMP, environmental health and safety, related guidelines, and internal policies and procedures. Specific duties will comprise material management, facility and equipment cleaning and maintenance, as well as production  activities typical for a cGMP pharmaceutical manufacturing operation; to include preparation of chemicals and components, formulation and filling of radiopharmaceutical products, and operation of equipment in a cleanroom environment. The preferred individual will possess sufficient technical, functional, and administrative competence to work largely independently, in a team environment, in order to meet clinical production demands.  

Primary Responsibilities/Accountabilities: 

Support the manufacturing  activities from internal product development and external sponsorsReceive, sample, store and/or distribute all materials required for production Facilitate day-to-day operation and maintenance of the facility, production equipment, and testing instrumentation.  Perform hands-on execution of manufacturing procedures, following standard operating procedures (SOPs) and master batch records (MBRs)Lead and/or support investigations and documentation of deviations and exceptionsClean and maintain all production  equipmentRecord and maintain systems regarding cGMP compliance such as consumable inventory levels, area classification requirements, or site environmental monitoring

Communicate all issues related to safety, quality, and compliance to site leadership

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