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 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 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 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 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 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 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 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.