By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.Job DescriptionSummary:The incumbent is a member of the production scheduler team within the LA site. As the production scheduler, he/she will be responsible for creating and updating B5 (Fractionation) daily production schedule and B8 (buffer prep, Albumin, AHF, and Pilot Plant) production schedules in the assigned shift. The production scheduler will ensure the accuracy of the schedule and identify opportunities to minimize delays and to optimize manufacturing processes. The incumbent will work together with manufacturing team members as well as support group members. Direct interactions with contractors, vendors, suppliers, and customers may also be necessary.Essential Duties and Responsibilities:* Create and update daily production schedules (Fractionation, Purification) for manufacturing* Create advanced, weekly production schedules for all manufacturing departments* Schedule non-production related activities such as sanitization, rinse sampling, PM, corrective maintenance, engineering, and/or validation projects* Attend supply chain and maintenance planning meeting to forecast weekly production* Create mock schedules based on alternate production conditions/scenarios for management as necessary* Identify improvement opportunities in the schedule or in the process as related to WIP management* Recommend solutions to optimize processes and to minimize delays in the production* Interface with production scheduling tools (Excel and/or other system), DeltaV, EBM, and other supporting tool* Collect data and perform data analysis related to WIP, cycle time, lead time, etc* Participate in critical safety and continuous improvement related activities in the site* Perform other support activities for production needs as necessaryQualifications:* Good written and verbal communication skills in English and understanding of cGMP regulations* Must be able to read and follow detailed written instructions* Math and computer skills (Microsoft Office programs such as Powerpoint, Excel, Word, Project)* Experience in DeltaV, EBM, scheduling software, or similar systems* Must be able to complete tasks with minimal supervision, prioritize multiple tasks, and manage time effectively* Detail oriented and effectively organize documentation for review* Must be able to independently recommend and suggest solutions* Good interpersonal skills to work effectively and efficiently in a team environment* Multi-tasking abilityEducation and/or experience:* High school diploma or GED. 4+ years of related work experience or AA degree or higher and 2+ years related work experiencePhysical Demands:* Must be able to lift, push, pull and carry up to 15 lbs* In general, the work requires a substantial amount of sedentary work that includes typing and computer interactions with some walking around observing conditions in the facilityWorking Environment:* Must be able to work in controlled environments requiring special gowning. Will be required to follow gowning requirements and wear protective clothing over the head, face, hands, feet, and body* No make-up, jewelry, contact lenses, nail polish, or artificial fingernails may be worn in the manufacturing environment* Will work in a cold, wet environment* Must be able to work multiple shifts, including weekends* Must be able to work overtime as required* May be required to work in a confined area* Some clean room and cool/hot storage conditionsThis job posting excludes CO applicants.LocationsUSA – CA – Los AngelesWorker TypeEmployeeWorker Sub-TypeRegularTime TypeFull time