of Position Perform assigned laboratory testing and related quality control activities in order to ensure compliance with applicable SOP's and cGMPs. Provide timely testing and notification of any aberrant occurrence to Management / Supervision that presents potential negative impact to manufactured or marketed product. Work under limited supervision with considerable lati

of Position The Quality Assurance Specialist position reports directly to the Manager Quality Assurance. The Quality Assurance Specialist is responsible for implementing and supporting the Quality Management System (QMS) in accordance with Company policies and procedures. Schedule Monday Friday 8am 5pm Essential Functions Write, revise, review, and approve site procedures

of Position The People Partner opportunity is great for individuals with several years of Recruiting, Talent Acquisition or HR Generalist experience! We are seeking a Human Resources People Partner to support the alignment of our HR initiatives and functions with business objectives and employees in designated business units while continuing to grow your HR experience. The

of Position The role of a Manufacturing Technician is to perform all tasks associated with formulation, preparation, assembling, and packaging of components, according to cGMP Guidelines to meet production demands. The Manufacturing Technician will have knowledge of the manufacturing process and serve as one of several technicians while coordinating work within the standar

of Position Perform assigned quality control activities within the Microbiology Department in order to comply with applicable SOP's and cGMPs. Work under limited supervision with considerable latitude for the use of initiative and independent judgment. Provide timely testing and notification of any aberrant occurrence to Management / Supervision that presents potential neg

of Position Provide dedicated and focused technical support on the unique IT architecture, hardware and software solutions supporting the manufacturing plant located in Noblesville, IN. Participates in IT's responses to production issues and works closely with the Service Desk on reported incidents or requests that involve the plant's restricted areas and isolated network.

of Position Responsible for independently addressing equipment upgrades and improvements through process improvements and via the use of capital project execution. Responsible for design, construction, and maintenance of the plant control, electrical infrastructure systems, and process equipment. Performs electrical/controls design changes; design, build, and install upgra

of Position The Senior Manager of Regulatory Affairs is responsible for Nuclear Medicine Regulatory Affairs dossiers and associated regulatory affairs activities in the US. The responsibilities include, yet are not limited to, defining and or authoring compliant content for new and existing dossiers, implementing and managing tracking systems, and preparation of electronic

of Position Perform assigned quality control activities within the Microbiology Department to comply with applicable SOP's and cGMPs. Work under limited supervision with considerable latitude for the use of initiative and independent judgment. Must have the ability to work collaboratively, multitask, and adapt to changing priorities and schedules. Schedule Monday Friday 4p

of Position The Senior Quality Control Testing Engineer role is responsible for supporting the Quality Control organization in conducting investigations, change management, identifying and implementing continuous improvement opportunities, and maintaining GMP compliance. Schedule Monday Friday 8am 4 30pm Essential Functions Support or serve as lead investigator for Out of

of Position The Senior Quality Control Testing Engineer role is responsible for supporting the Quality Control organization in conducting investigations, change management, identifying and implementing continuous improvement opportunities, and maintaining GMP compliance. Schedule Monday Friday 4pm 12 30am Essential Functions Support or serve as lead investigator for Out of

of Position The Senior Manufacturing Chemist position will serve as part of the production team responsible for the processing of bulk radiopharmaceuticals including production preparation and equipment maintenance activities in a highly regulated (FDA/NRC) environment. This position is in our Noblesville, Indiana location. Work Schedule Monday Friday 8 00am 4 30pm. Abilit

of Position Perform routine environmental monitoring of aseptic processing and controlled area cleanroom environments used for pharmaceutical manufacturing. Perform assigned quality control or quality assurance activities in compliance with applicable SOP's and cGMPs. Schedule Monday Friday 12am 8 30 am Essential Functions Ensure a safe and quality working environment thro

of Position To support preventative maintenance and repairing of production equipment and special projects as required of the manufacturing department. Perform a variety of duties in electronic, mechanical, electromechanical, pneumatic, hydraulic, or optical areas, including troubleshooting, adjusting, testing, and maintaining manufacturing equipment, components, devices,

of Position The Quality Assurance Engineer role is responsible for supporting the Quality organization by providing Quality Support on the Production Floor, conducting investigations, change management, identifying and implementing continuous improvement opportunities, and maintaining GMP compliance. The position reports directly to the Quality Assurance Manager at the Nob