This position operates on a 2 2 3 schedule, with 7 00 pm 7 00 am shifts. The Manufacturing Supervisor leads a team of manufacturing associates to perform upstream or downstream processing of bulk intermediates and/or bulk drug substances for biopharmaceutical products. The Supervisor will plan, assign, and monitor daily tasks to ensure timely "Right First Time" execution

Coordinate and perform cGMP manufacturing operations for manufacturing biopharmaceutical products. Ensure the effective use of material, equipment, and personnel while making products at high quality levels Position Responsibilities Assist in the execution of procedures for microbial manufacturing, purification, or support area of manufacturing using SOP's and batch recor

The Operational Excellence (OpEx) Senior Specialist or Manager will support the site's portfolio of continuous improvement initiatives, activities, and high value projects. The Sr OpEx Specialist will manage several projects concurrently, coach leaders through the successful execution of improvement events, and capture significant sustained value for our customers. The Sr

Open position available in Rapid Analytics group, a highly technical team in a dynamic work environment. Responsible for performing contract development services specializing in particle and biophysical characterization to support formulation, analytical development, and stability programs. Position Responsibilities Perform characterization with techniques such as HPLC, c

The Senior Manufacturing Associate I/II is responsible for performing upstream processing of bulk intermediates and/or bulk drug substances for biopharmaceutical products. The Senior Manufacturing Associate must follow written, approved procedures and forms to ensure all work is conducted "Right First Time" (RFT) following Good Manufacturing Practices (GMP), Good Document

Open position available in Rapid Analytics, a highly technical team in a dynamic work environment. Responsible for performing contract development services specializing in biophysical and particle characterization to support formulation, analytical development, and stability programs. Position Responsibilities Proficiency with biophysical, biochemical and biopharmaceutica

This position is on a 2 2 3 shift, with the hours 7p 7a. The Sr. Manufacturing Associate I/II Downstream is responsible for the execution of production activities for early and late phase Cell Culture programs within a GMP environment. The Sr. Manufacturing Associate I/II Downstream must follow the instructions depicted in SR's, EPR's, BR's, SOP's and forms. Additionally,

The Associate Director, Validation is accountable for validation activities at the KBI Boulder facility for the following disciplines Facilities qualification Utilities qualification Equipment qualification GAMP 3 5 automation qualification including Part 11 Cleaning validation including changeover equipment strategies Steaming validation Air visualization validation Prod

This position operates on a 2 2 3 schedule with the hours 7 00 am 7 30 pm. The Manufacturing Assistant position is designed as an introduction to the industry of cGMP manufacturing. This position performs all routine/non routine cleanings and maintains gowning supplies for the locker rooms and gowning rooms at the CMF GMP facility to support continuous manufacturing opera

The Supply Chain Operations Analyst (Intern) is accountable for the design and execution of demand planning and order forecasting, supply planning, product deployment and expediting processes and the development and implementation of a stocking optimization model to minimize costs and inventory while delivering on service requirements. Position Responsibility Research and

This position performs all dispensing and sampling of raw chemicals needed to support the manufacturing facility. This position requires a shift schedule and gowning into a clean room environment. This position requires PPE. Must be able to lift 50 pounds. Must be able to document, and record activities in electronic systems and comply with regulatory requirements, cGMPS,

The Facilities Engineering Department is responsible for all aspects of maintaining the site infrastructure in an active reliable state to support cGMP operations. Facilities Engineering oversees the architectural features of the buildings, Structural/Civil, Biotech process and laboratory equipment and systems, HVAC, Plant and Clean Utility Systems, Electrical Power and L

The Microbiology Senior Associate will be part of the Microbiology Department responsible for the testing and support for the Microbiology Laboratory in support of a Contract Manufacturing biotechnology facility and Process Development. Responsibilities includes laboratory support, program testing, reporting of results, development and execution of protocols and reports.

The Facilities Engineering Department is responsible for all aspects of maintaining the site infrastructure in an active reliable state to support cGMP operations. Facilities Engineering oversees the architectural features of the buildings, Structural/Civil, Biotech process and laboratory equipment and systems, HVAC, Plant and Clean Utility Systems, Electrical Power and L

The Microbiology Associate will be part of the Microbiology Department responsible for the testing and support for the Microbiology Laboratory in support of a Contract Manufacturing biotechnology facility and Process Development. Responsibilities includes laboratory support, program testing, reporting of results, execution of protocols. This person is responsible for the