The Full Stack Senior Software Engineer will enhance our web application user interfaces, services and data model while working closely with platform engineers. You will be influential in maintaining the current product as well as influencing and developing the next generation of the product. In addition, you will contribute to the overall design and development of other

Designs, develops, implements and supports all aspects of electrical control systems, equipment, and machinery related to site utilities, production equipment, and facilities. Is a technical resource to the Engineering, Maintenance and Validation departments to meet all regulatory and company specific policy requirements and to improve plant efficiency, capacity, and capa

The Production Group Leader will be responsible for all daily operations of functional department without direct supervision on the shift. Responsible for training all employees on that shift, allocating resources, scheduling shift activity and insuring cGMP compliance in operation. This cross functional role is also responsible for assembling, operating, and monitoring s

POSITION SUMMARY The Master Technician provides direct engineering and maintenance support for processes and equipment used to compound, fill, process, sterilize and finish pharmaceutical products in a cGMP compliant manner. He/She will collaborate with multiple site functions to implement new equipment and processes. The incumbent is a key contributing member to the manu

The Principal Engineer, Software ClinApp designs and implements Fresenius Kabi software applications to achieve product functionality needs and business objectives. Responsibilities Under minimal guidance performs, design and develops software applications and/or processes within established medical product design controls. The Principal Engineer, Software will improves s

Responsible for providing technical support to operations in terms of initial equipment/facility/utility qualifications and equipment/facility/utility requalifications. Will participate in process and equipment improvement teams charged with enhancing the compliance and performance of plant systems, while considering the regulatory requirements for change control. Individ

POSITION SUMMARY The Warehouse Operator Level 2 is responsible for, but not limited to, the accurate picking of orders of material for production and packaging. These orders include tasks generated by production, packaging, and formulation for materials used in commercial and non commercial batches. The wrapping, movement, labelling, and storage of semi finished and finis

Responsible for an intermediate level of expertise in analytical chemistry, chromatographic methods of analysis and instrumentation, including troubleshooting. Independently executes protocols, verifications, method transfers in support of senior level personnel. Directs and provides guidance to associate scientists. Responsibilities Be able to articulate work related iss

Responsible for working in packaging in order to maintain a steady flow of production. This may involve the following loading and unloading tubs and moving pallets. Must follow SOP's and any departmental procedures. Recommends improvements and identifies potential problems which could affect the operation both personnel and equipment related. This position reports to the

A Scientist II in Quality Control displays an advanced knowledge in chromatographic techniques and instrumentation, and guides others in troubleshooting instrumentation and routine test methods. A Scientist II participates in the mentoring and training of less experienced analysts in the group. Responsibilities Principal Activities and Responsibilities Be able to articula

Responsible for the full set up and safe, clean, efficient and consistent operation of Inspection and Packaging equipment and all associated documentation. Must be knowledgeable of and able to operate all packaging lines with HMI applications. This position requires extensive amounts of leadership, decision making and coordination of co workers. This position reports to t

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 Visually inspec

Responsible for working in packaging in order to maintain a steady flow of production. This may involve the following loading and unloading tubs and moving pallets. Must follow SOP's and any departmental procedures. Recommends improvements and identifies potential problems which could affect the operation both personnel and equipment related. This position reports to the

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 working in packaging in order to maintain a steady flow of production. This may involve the following loading and unloading tubs and moving pallets. Must follow SOP's and any departmental procedures. Recommends improvements and identifies potential problems which could affect the operation both personnel and equipment related. This position reports to the