31 to 45 of 49
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
Posted 15 days ago
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
Posted 17 days ago
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
Posted 17 days ago
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
Posted 17 days ago
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
Posted 17 days ago
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
Posted 18 days ago
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
Posted 18 days ago
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. Schedule Saturday Tuesday 7pm 5 30am Essential Function
Posted 18 days ago
of Position Performs all tasks associated with the preparation, formulation, sterilization, dispensing, inspecting, labeling, and packaging of manufactured products according to cGMP Guidelines in order to meet production demands. Performs all tasks associated with the Sterile Core production area as well as providing backup support for the Cold Products Packaging and Asep
Posted 18 days ago
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
Posted 19 days ago
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. May supervise the work of others and coordinate instrum
Posted 21 days ago
of Position The role of a Senior Manufacturing Technician is to perform all tasks associated with operating equipment through formulation, preparation, and dispensing of aseptic fill radiopharmaceutical processes, according to cGMP guidelines to meet production demands. The Senior Manufacturing Technician will work with advanced automated equipment, in the creation of new
Posted 22 days ago
of Position The Director of Marketing based in the North American corporate office in St Louis, MO, is responsible for the planning and execution of marketing strategies designed to optimize the financial performance of the Nuclear Medicine business. This responsibility includes managing the product portfolio, developing and executing marketing strategies to protect and gr
Posted 22 days ago
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 Combination of 1st and 2nd shift, 5 week rotating schedule repeating the following schedule Week
Posted 23 days ago
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
Posted 23 days ago
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