Sr. Chemist, Nuclear Manufacturing

Cardinal Health•Indianapolis, IN

13d

About The Position

What Nuclear Manufacturing contributes to Cardinal Health Nuclear Manufacturing is responsible for the manufacturing of time sensitive radiopharmaceuticals in an integrity driven, highly regulated environment (i.e. FDA, NRC, DOT) to support patient treatment through disease diagnosis, staging, and monitoring. Shift/Schedule The facility typically operates during normal business hours (Monday-Friday, 8 AM to 5 PM) Flexibility to work periodic off-shift hours in support of routine production and testing needs

Requirements

2-4 years of experience, preferred
Bachelor's degree in related field, or equivalent work experience, preferred
Bachelor’s degree in engineering or a physical science with at least two years of experience working in a GMP environment in the pharmaceutical or biotechnology industry preferred
Demonstrated familiarity with the operation, use and cleaning of laboratory scale production equipment and conventional analytical instrumentation
Ability to work in a controlled environment requiring special attention to environmental, health, and safety regulations
Commitment to maintain data integrity through strict adherence to standardized procedures and relevant compliance requirements; ability to clearly document all work activities in a timely manner
Motivation to work effectively and cooperatively with others, and to establish and maintain good working relationships
Applies working knowledge in the application of concepts, principles and technical capabilities to perform varied tasks
Works on projects of moderate scope and complexity
Identifies possible solutions to a variety of technical problems and takes action to resolve
Applies judgment within defined parameters
Receives general guidance and may receive more detailed instruction on new projects
Work reviewed for sound reasoning and accuracy

Responsibilities

Support the transfer of all manufacturing and testing activities from internal product development and external sponsors.
Receive, store and distribute all materials required for production and testing.
Facilitate day-to-day operation and maintenance of the facility, production equipment, and testing instrumentation.
Perform hands-on execution of manufacturing and/or testing procedures.
Lead and/or support investigations and documentation of deviations and exceptions.
Clean and maintain all production and related testing equipment.
Communicate all issues related to safety, quality, and compliance.