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 role of a Senior Manufacturing Technician is to perform all tasks associated with formulation, preparation, assembling, and packaging of components (V4 Generators), according to cGMP Guidelines in order to meet production demands. The Senior Manufacturing Technician will have advanced knowledge of the manufacturing process and serve as one of several lead t

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 Process Engineer Active Pharmaceutical Ingredient (API) Hot Products provides technical discipline and leadership required to maintain, plan, and implement robust and capable cyclotron derived API manufacturing processes, as well as upstream process activities for North America. This role will be responsible for performing the following identifying a

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 The R&D Technical Writer position will report to the Senior Director of Downstream R&D. The successful candidate will serve as a technical team member and will support the drafting technical documents and development reports consistent with the project schedule. Essential Functions Prepares written project documents, including reports, memoranda, and SOPs. Auth

of Position The Associate Development Engineer position will work in the Downstream R&D group, and will report to the Director of Downstream R&D. The successful candidate will be responsible for new product development activities, as assigned, which includes development and execution of R&D protocols consistent with Product Transfer Process, and supporting manufacturing in

of Position The Principal Quality Assurance Engineer is responsible for the oversight and primary SME for quality assurance and validation for new products / projects. This position requires strong technical and training skills of quality systems. The position reports directly to the Senior Director of Site Quality. Knowledge in pharmaceutical quality systems with proficie

of Position The Manufacturing Technician produces the Active Pharmaceutical Ingredient for cyclotron based radiopharmaceuticals through purification of starting materials by means of chemical processing. This work is conducted in cGMP and NRC compliant laboratories utilizing advanced equipment in the creation of new products. Work Schedule Saturday Tuesday 8 00pm 6 30am. A

of Position The Manufacturing Technician produces the Active Pharmaceutical Ingredient for cyclotron based radiopharmaceuticals through purification of starting materials by means of chemical processing. This work is conducted in cGMP and NRC compliant laboratories utilizing advanced equipment in the creation of new products. Work Schedule Saturday Tuesday 8 00pm 6 30am. A