1. Create excel spreadsheet to support Nitrosamine Risk Assessment for all US products 2.Data collection from various sources, such as SAP, Documentum/eDMS, Regulatory database, external manufacturer documentation 3.Needs to collaborate with various functions within the organization Compensation $20.50/hr $24.50/hr depending on level of education Responsibilities Student

The ISO Systems and Sustainability Manager is responsible for the management and maintenance of all the local requirements under ISO 14001 Environmental Management System (EMS), ISO 45001 Occupational Health and Safety Management System (OHSMS), and ISO 50001 Energy Management System (EnMS) for the Plant (Production Unit) in accordance to the current ISO Standards, as wel

The Sr Principal Engineer performs sustaining engineering activities and technical project management related to disposables / consumable products for the Ivenix Infusion System portfolio. Apply specialized knowledge to manage and complete complex projects, including design and/or process related activities. Develop strategies where clear guidelines do not exist and creat

The Sr Principal Engineer performs sustaining engineering activities and technical project management related to commercial infusion pump products for the Ivenix Infusion System portfolio. Apply specialized knowledge to manage and complete complex projects, including design and/or process related activities. Develop strategies where clear guidelines do not exist and creat

The Clinical Implementation Specialist is a registered nurse (RN) responsible for the successful implementation of medical device(s)/infusion pumps at customer locations. This role serves as a clinical educator to Fresenius Kabi's customers (nurses and clinical staff) on the appropriate use of our IV Therapy products and solutions. The Clinical Implementation Specialist a

The Senior Director, Medical Affairs will provide global medical leadership for the R&D function of the Fresenius Kabi MedTech business, which includes medical devices and solutions associated with transfusion, cell therapies, and infusion technology. Participate in and guide risk management inputs for development projects, support definition and execution of clinical dev

The Vice President, Medical Affairs is responsible for leading the development and execution of strategic and tactical plans for Headquarter (HQ) and Field medical affairs teams pre launch, launch, and post approval for biosimilars and biologic products. This leader is an active and collaborative member of the Biosimilar Leadership Team (BLT). Leads local and collaborates

Responsible for visually inspecting filled product off the filling line following Standard Operating Procedures (SOP) and current Good Manufacturing Processes (cGMP). The production inspector will work in the Capping Department and on the off line inspection area and therefore must be knowledgeable of procedures and equipment in each area. Responsibilities We offer state

An Associate Scientist is responsible for performing entry level chemical testing to support raw material, in process, stability, and finished products as required for Quality Control. Effectively communicates work and results both orally and in writing. Responsibilities Able to articulate work related issues clearly and effectively to management and peers Perform accurat

The Project Manager is responsible for the effective management (organization, financial/project planning, execution, control and evaluation) of all aspects of assigned projects. The Project Manager will effectively collaborate with project governance boards, communicate project status to management and provide resolution of project issues. This position requires a dynami

POSITION SUMMARY Responsible for the installation, maintenance, and modification of all site facilities and utilities. Responsible for repairs, troubleshooting, calibration, and preventative maintenance of associated systems and equipment to include all process utility equipment. Responsible for maintaining good operating condition of equipment used in support of the manu

POSITION SUMMARY Responsible for the installation, maintenance, and modification of all site facilities and utilities. Responsible for repairs, troubleshooting, calibration, and preventative maintenance of associated systems and equipment to include all process utility equipment. Responsible for maintaining good operating condition of equipment used in support of the manu

POSITION SUMMARY The Master Technician provides direct engineering and maintenance support for facility and utility processes and equipment to support the manufacturing of pharmaceutical products in a cGMP compliant manner. He/She will collaborate with multiple site functions to implement new equipment and processes. Responsible for repairs, troubleshooting, calibration,

The Sr. Manager, FDA Compliance (Global Remediation Officer) assures that all plants and I&D Centers having activities with US FDA are in compliance with US FDA regulations, including but not limited to, cGMPs, cGLPs, & cGCPs. This includes foreign facilities within Fresenius Kabi for importation of API or finished products to the US market. This position organizes and pr

The Principal Validation Engineer plays a pivotal role as a subject matter expert within Manufacturing Operations, fostering collaboration across quality, regulatory, manufacturing, engineering, and global R&D teams. This individual is entrusted with providing technical support for equipment/system validation and requalification, while actively participating in equipment