The specialist has responsibility for the implementation of the environmental, health, safety, and sustainability (EHS&S) program. This includes leadership to maintain EHS&S compliance and continuous improvement. EHS&S supports operations of biologic contract development and manufacturing organization. Responsibilities include incident response, reporting and investigatio

Responsible for providing Metrology support and services to KBI's internal operations at a 24/7 KBI Biopharma manufacturing site. Serves as primary source of calibration services for all customer requirements including planned and unplanned calibration activities. Position Responsibilities Inspect, calibrate, troubleshoot, repair, and maintain equipment and instrumentatio

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

The Maintenance and Facilities Manager is responsible for ensuring buildings, equipment and systems are maintained and fit for use. The Manager oversees day to day maintenance and calibration operations including planning and scheduling, coordination of work order execution, troubleshooting and problem solving, and ensuring quality and completeness of all associated docum

Reviews data associated with development and qualification of analytical methods and testing of in process and drug substance/product samples. Position Responsibilities Reviews data and reports associated with development and qualification of analytical methods and testing of in process and drug substance/drug product samples. Verifies that calculations and documented inf

The role of the program manager is to manage cross functional teams responsible for delivering defined project outputs on time, within budget and importantly with quality results. Manager will need to plan, organize, monitor and oversee multiple projects to meet sometimes difficult to define requirements. The manager is able to react to change productively and handle othe

Assures that suppliers and raw materials are suitable for their intended use in the manufacture of clinical and commercial biologics bulk drug substance. Responsible for compliance with regulations, procedures, and systems that govern the supplier approval and material qualification programs. Supports client audits and regulatory inspections. Position Description SQM assi

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.

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

This individual will provide management and thought leadership expertise to the IT Validation and Compliance team that consists of direct reports at a senior and principle level as well as managed validation service resources in a Contract Development and Manufacturing Organization (CDMO) setting. Individual will ensure that adequate resources and processes are in place t

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 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

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 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 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