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KBI Biopharma Manufacturing Manager, Day Shift in Boulder, Colorado

Job DescriptionResponsibilities:Manages the respective activities related to cGMP manufacturing, includingthe development and implementation of manufacturing methods, processes andoperations for manufactured biopharmaceutical products. Ensures the effectiveuse of material, equipment and personnel while producing products at highquality levels. Manages daily manpower requirements.Execute manufacturing requirements by meeting or exceeding productivity,quality and capacity objectives as set forth by management. Manage dailyschedules of production activities, outline staff assignments, materialand equipment requirements, and training needs. Assist staff with on thefloor execution of production tasks.In cooperation with customer representatives, process development andmanagement personnel, look for opportunities to improve operations. Closelycoordinate potential process improvements with quality and regulatory toassure cGMP compliance.Hire, develop and motivate manufacturing operators. Assure continualtechnical development of staff. Conduct bi-annual performance reviews forstaff. Conduct more frequent reviews for new hires and personnel who haveshown performance deficiencies.Assist with management of production/operation planning and scheduling.The responsibilities of this position include hazardous and non-hazardouswaste handling.Qualifications:Bachelor's degree in a related scientific or engineering discipline and 7years pharma experience (fermentation, cell culture, purification);or 7+ years related experience and/or training; or equivalentLifting up to 50 lbs, walk and stand 50% of the time, Sit 50% of the time.Must be able to hear equipment alarms.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.

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