KBI Biopharma Senior Manufacturing Associate I/II in Boulder, Colorado
Job Description:Coordinate and perform cGMP manufacturing operations for biopharmaceuticalproducts. Ensure the effective use of material, equipment andpersonnel while making products with the highest quality.Execution of procedures for microbial manufacturing without minimalsupervision and provide work direction to less experienced staff. Act as shiftlead when necessary.Must have in-depth knowledge and expertise in area equipment/systems, aswell as independently and fully developed troubleshooting skills ofequipment/ processes.Maintain records to comply with regulatory requirements, cGMPs and SOP's.Provide technical input of validation protocols, including development,execution, and summary. Ability to provide technical input into BatchRecords revisions.Train area personnel in one or more areas of expertise including advancedskills.Experience:Sr. Mfg. Associate I: Minimum HS/GED and 7 years related industryexperience; or Associate's degree and 6 years related industryexperience; or BS/BA and 4 years or equivalent combination of educationand experience.Sr. Mfg. Associate II: Minimum HS/GED and 9 years related industryexperience; or Associate's degree and 8 years related industryexperience, or BS/BA and 6 years of related industry experience.Manufacturing experience in biotechnology, including fermentation,purification, solution preparations, and mechanical troubleshooting skills.KBI Biopharma, Inc. is an EEO/AA employer and actively seeks to diversifyits work force. Therefore, all qualified applicants, regardlessof race, color, national origin, religion, gender, genderidentity, sexual orientation, age, disability or veteran status, arestrongly encouraged to apply.