The Manufacturing Specialist I/II is responsible for supporting equipment and cGMP operations for the Upstream team in a large scale biopharmaceutical facility. The manufacturing specialist has experience in upstream unit operations (see expansion, bioreactor operations, cell culture harves), and a working knowledge of upstream equipment. The incumbent will have knowledge

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

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

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

This position operates on a 2 2 3 schedule with the hours of 7 00 am 7 30 pm. The Manufacturing Associate I/II (Manufacturing Associate) is responsible for performing upstream or downstream processing of bulk intermediates and/or bulk drug substances for biopharmaceutical products. The Manufacturing Associate must follow written, approved procedures and forms to ensure al

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

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

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 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

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

Identifies, evaluates, develops and closes new customers and expands business at existing customers. Identifies and assists in progressing biopharmaceutical business opportunities including new scientific and strategic partnerships, collaborations, licensing opportunities, joint ventures and alliances. Establishes and implements appropriate development strategies to suppo

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

Seeking a highly motivated and detail oriented intern to assist with data cleanup in our Salesforce instance. This internship opportunity will provide valuable experience in data management and contribute significantly to the enhancement of our overall operational efficiency. Term May 20th August 9th, 2024. Responsibilities The intern will be responsible for Identifying a

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 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