of Position The Regulatory Affairs Technical Writer supports projects related to Curium's business strategy in the space of sterile drug manufacturing including reactor and cyclotron derived new products. This position focuses on the creation, revision, and maintenance of technical documentation necessary for regulatory submissions and compliance within a regulated industr

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

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 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 Provide validation support for site product development, process improvement, and regulatory compliance initiatives as Subject Matter Expert and corporate liaison for one or more of the following areas Lyophilization, Sterilization Autoclaves and Depyrogenation ovens, VHP, Isolators, Computer Systems, Cleaning, Process, Automated Fillers, Stopper Processors, CI

of Position The Manager Quality Control is responsible for ensuring accountability, transparency, and effective communication cross functionally and within his/her team while ensuring information is timely, clear and accurate. Coaching and developing will foster team ownership that ensures compliance with all policies, procedures and regulations. Must ensure maintain opera

of Position The Quality Control Instrumentation Manager is responsible for leading the implementation, and optimization of analytical instrumentation within the Quality Control department. This role involves hands on project management through to operational readiness. The ideal candidate will possess a deep technical understanding of analytical techniques, project managem

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 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 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