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

Perform preventative maintenance, corrective maintenance and troubleshooting on process equipment and utility systems, electrical, plumbing, mechanical (HVAC) systems following written Standard Operating Procedures within a cGMP manufacturing environment. Must have strong mechanical aptitude to support maintenance of specialized production equipment, plant utilities, and

This position is on a 2 2 3 schedule, 7p 7a. The Sr. Manufacturing Associate I/II Upstream 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 Upstream must follow the instructions depicted in SR's, EPR's, BR's, SOP's and forms. Additionally, must ensure all

The 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. Position Responsibilities The Manufacturing Associate I/II Downstream must follow the instructions depicted in SRs, EPRs, SOPs and forms. Additionally, must ensure all work is conducted following Goo

The downstream manufacturing associate will participate in the purification areas for a clinical and commercial GMP biopharmaceutical facility. The associates will perform production activities while safeguarding work environments, employing cGMP compliant behaviors, and following principles to ensure 'Right the First time' execution. The ideal candidates can demonstrate

The downstream manufacturing associate will participate in the purification areas for a clinical and commercial GMP biopharmaceutical facility. The associates will perform production activities while safeguarding work environments, employing cGMP compliant behaviors, and following principles to ensure 'Right the First time' execution. The ideal candidates can demonstrate

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.

Manages the respective activities related to cGMP manufacturing, including the development and implementation of manufacturing methods, processes and operations for manufactured biopharmaceutical products. Ensures the effective use of material, equipment and personnel while producing products at high quality levels. Manages daily manpower requirements. Execute manufacturi

Responsible for coordination, modification, engineering and design of company facilities and equipment. Direct concurrent engineering projects both technical and project management aspects for capital projects while ensuring their success in meeting their respective objectives. Technical aspects include Architectural features, Structural/Civil, Biotech process and laborat

To support KBI's digital transformation, the Digital Product Owner III leads the creation and/or the expansion of one of our digital products which supports one or more of KBI's business units to sustain or improve the efficiency of the processes of that business or the company as a whole. This leadership role in our Digital Transformation journey bridges our company's pr

Responsible for providing financial assistance in order to ensure effective, efficient and accurate financial and administrative operations. Processing PO and Non PO invoices Responding to Supplier emails within a 24 to 48 hour timespan Ensuring that 90% of your suppliers are paid per terms Creating process improvements that improve the department efficiency Partner with

Manages all activities related to the planning, purchase, receipt, warehousing, and distribution of supplies and materials used in the company's development, production, and administrative support functions. Position Responsibilities Execute the daily operations of inventory planning and procurement areas in the development and execution of short and long range production

This position operates on a 2 2 3 schedule with 7 00 am to 7 00 pm shifts. 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

This position is on 2 2 3 shifts, 7a 7p. MFG Support Associate I/II is responsible for the execution of production activities of Media and Buffer preparation within a GMP environment. The Manufacturing Associate I/II Support must follow the instructions depicted in SR's (Media / Buffer Solution Records), SOP's and forms. Additionally, must ensure all work is conducted fol

Quality Site Head at a contract manufacturer of mammalian cell culture protein therapeutics. Lead a Quality Assurance organization responsible for raw material inspection and release, QA on the floor, disposition of bulk drug substance, QA review of quality control data, and QA review of method validation, process validation, and equipment/utilities qualification. Quality