This position operates on a 2 2 3 day shift schedule. The Manufacturing Technician position is designed as an introduction to the industry of cGMP manufacturing. This position performs all routine/non routine cleaning of equipment, prepares buffers/medias, glass wash of misc. parts, assembles setups and filters, autoclaves media/materials, tests filter integrity, manages

Join a highly technical analytical team in a dynamic work environment as a member of the Analytical, Formulation and Stability (AFS) department and participate in contracted client analytical programs for monoclonal antibodies, recombinant proteins, and peptides. Perform testing services including GMP testing, analytical method transfer activities, analytical method quali

This position operates on a 2 2 3 night shift schedule. The Manufacturing Technician position is designed as an introduction to the industry of cGMP manufacturing. This position performs all routine/non routine cleaning of equipment, prepares buffers/medias, glass wash of misc. parts, assembles setups and filters, autoclaves media/materials, tests filter integrity, manage

This position is on a 2 2 3 shift, 7a 7p. The 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 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 work is co

This position operates on a 2 2 3 day shift schedule. The Manufacturing Technician position is designed as an introduction to the industry of cGMP manufacturing. This position performs all routine/non routine cleaning of equipment, prepares buffers/medias, glass wash of misc. parts, assembles setups and filters, autoclaves media/materials, tests filter integrity, manages

At KBI, we are creating planning processes to support the company's growth and position it as the next generation CDMO. The S&OP Master Planner II role is a unique role to lead global planning and execution of the key planning nodes. While each Master Planner would specialize in one planning node, the expectation is that the Planners will be cross trained to support the b

It is the expectation that this position is required to be onsite full time. Addition, this position should be in the laboratory/facility for a minimum of 40% time daily. Plan and review routine Microbial Laboratory work. Utilizes technical discretion in the execution and interpretation of experiments that contribute to program goals. May perform testing when required. St

Perform laboratory support functions such as sample log in and storage, issuance of controlled data forms, and monitoring of temperature controlled chambers in compliance with standard operating procedures, safety, and cGMP regulations. Responsible for all associated documentation and for maintenance of laboratory area. Position Responsibilities Manage cGMP system for inc

This Manufacturing Sciences and Technology (MS&T) Principal Engineer position will lead a team responsible for process development, and process transfer for clinical and commercial manufacturing. This person and their team will also have responsibilities for the ownership of processing equipment and unit operations, including system design, procurement, installation, and

The Sr. Director, Manufacturing oversees the management of all areas of the Manufacturing department, including the upstream processing (cell culture and harvest), downstream processing (purification and bulk filling), and manufacturing support teams. The overall aim is to produce bulk intermediates and/or bulk drug substances while achieving quality, schedule, and cost o

This position represents an opportunity to apply engineering expertise at the Engineer II level in the Manufacturing Sciences and Technology group in support of GMP production operations at the Boulder, Colorado manufacturing facility. Position Responsibilities Qualified candidates would have the ability to provide biological engineering principles to the process developm

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 work is conducted following Good Manufacturi

s (Balanced Score Card) for self and team Leads or contributes to departmental initiatives as appropriate , including procedure development and improvement Cross site portfolio leadership OR process ownership; work with PMO and local team to continuously improve PM and project delivery practices. May own a PMO process, responsible for training tools and associated change m

This position will be on a 4 3 night shift schedule. The hours are 7 00 pm to 7 00 am. 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 ma

The Senior Specialist has responsibility for the implementation of the Environmental, Health, Safety, and Sustainability (EHSS) program. This includes leadership to maintain EHSS compliance and continuous improvement. EHSS supports operations of biologic contract development and manufacturing organization. Responsibilities include incident response, reporting and investig