This position is on a 2 2 3 day shift schedule. The hours are 7 am to 7 pm. Coordinate and perform cGMP manufacturing operations for biopharmaceutical products. Ensure the effective use of material, equipment and personnel while making products with the highest quality. Position Responsibilities Execution of procedures for microbial manufacturing without minimal supervisi

This position will be on a 2 2 3 day shift schedule. The hours are 7 am to 7 pm. 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 manufact

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 night shift schedule. The hours are 7 00 pm to 7 00 am. Coordinate and perform cGMP manufacturing operations for biopharmaceutical products. Ensure the effective use of material, equipment and personnel while making products with the highest quality. Position Responsibilities Execution of procedures for microbial manufacturing without minimal s

This position will be on a 2 2 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

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

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 lead manufacturing associate is responsible for performing upstream or downstream processing of bulk intermediates and/or bulk drug substances for biopharmaceutical products. The lead manufacturing associate must follow written, approved procedures and forms to ensure all work is conducted "Right First Time" (RFT) following Good Manufacturing Practices (GMP), includin

This position is on a 4 3 day shift schedule. The hours are 7 am to 7 pm. Coordinate and perform cGMP manufacturing operations for biopharmaceutical products. Ensure the effective use of material, equipment and personnel while making products with the highest quality. Position Responsibilities Execution of procedures for microbial manufacturing without minimal supervision

This position will be on a 4 3 day shift schedule. The hours are 7 am to 7 pm. 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 manufactur

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

This position is on a 4 3 day shift schedule. The hours are 7 00 pm to 7 00 am. Coordinate and perform cGMP manufacturing operations for biopharmaceutical products. Ensure the effective use of material, equipment and personnel while making products with the highest quality. Position Responsibilities Execution of procedures for microbial manufacturing without minimal super

We are currently seeking a highly motivated and detail oriented individual to fill the role of Technical Lead, Contract Manager within KBI's Global Business Development Team. In this dynamic position, you will collaborate closely with the legal department, business development representatives, proposal writers, and other teams across various business segments. The role in

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

The Microbiology Assistant 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 and program testing. Position Responsibilities The Microbiology Assistant will be part of the Micro