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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
Posted Today
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 Today
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 Today
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 Today
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 Today
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 1 day 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 1 day 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 1 day 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. Work under limited supervision with considerable lati
Posted 1 day 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 1 day ago
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
Posted 1 day 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 2 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 4 days ago
of Position 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, maintaining manufacturing equipment, components, devices, or syst
Posted 4 days ago
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
Posted 5 days ago
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