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

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

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

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

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

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

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

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 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.

This position is accountable for managing assigned inventories through daily, weekly, monthly, and annual physical counts. The Inventory Analyst organizes and partners in conducting periodic inventory counts, adjusts quantities and locations, records and reports discrepancies to management while maintaining communication with supported internal customers. Will be the lead

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

Assist with and support execution of routine procedures within the manufacturing area. Position Responsibilities Order and stock general supplies in the manufacturing production areas Wash glassware/labware and clean equipment Perform GMP cleaning of suites as required Maintain records to comply with regulatory requirements, cGMPs, and SOPs The responsibilities of this po

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

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 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