The Upstream MS&T Engineer III will apply sound scientific and engineering principles to successfully transfer and enroll new biopharmaceutical processes into the cGMP manufacturing facility. The scope of this role includes Leading technical transfer projects for challenging mid late stage clinical manufacturing programs and commercial programs Driving business decisions

Candidate must have strong mechanical aptitude to support maintenance of specialized production equipment, plant utilities, and HVAC systems in accordance with established guidelines and Standard Operating Procedures. Perform general facility support activities including safety system inspections, personnel relocation, and general site maintenance and repair as required.

Responsible for executing experimental protocols andperforming elementary data analysis in biopharmaceutical development laboratories. Job Description Regularly exercises technical discretion in the execution and interpretation of experiments that contribute to project goals. Makes detailed observations and carries out elementary data analysis. Understands experiments and

Primary r esponsi bility writing and editing detailed technical proposals and project plans for KBI services . Proposals cover contract process development , analytics, and GMP manufacturing of biotherapeutics. Collaboration with cross functional teams including Business Development, Process Development, Analytical Development, Manufacturing, and Program Management teams

This individual will provide QA oversight of the Deviations, CAPA and Complaints organization. The Sr. Manager and works closely with the Program Management team to facilitate communications between KBI and clients regarding quality related events. The role will develop and maintain the Quality Assurance staff by recruiting, training, and managing team member. Position Re

This Quality position collaborates with Manufacturing, MS&T, Facilities Engineering, Supply Chain, and IT to ensure completion of Root Cause Analysis, CAPAs and Effectiveness Checks (ECs) for Deviations according to cGMP requirements and the company's SOP. The role is directly responsible for review and approval of Deviations, CAPAs and ECs and provides the support for ti

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

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 Microbiology 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, execution of protocols. This person is responsible for the

Please Note This position operates on a night shift 2 2 3 schedule and will be eligible for shift differential. Position Summary 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 Associa

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

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

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

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

We are currently seeking a highly motivated and detail oriented individual to fill the role of Inside Sales Sr. Technical Lead. This position will report to the Associate Director, Contracts, Inside Sales, and Analytics and will be responsible for prospecting, lead generation, and lead management. Through effective prospecting, they will build and expand the corporate cli