Master Scheduler Salary at Gcm BETA

Position Summary: The Care Coordinator is responsible for managing the coordination of patient visits, ensuring that the scheduling system and electronic medical records (EMR) are maintained accurately and up-to-date. This role involves the careful assignment of patients to appropriate clinicians, taking into account factors such as language, culture, and specific patient requests. The coordinator communicates scheduling changes promptly between office and field staff, monitors system messages, and responds appropriately in a timely manner. The Staffing Coordinator plays a vital role in ensuring the delivery of high-quality care to patients and their families. Essential Duties and Responsibilities: Is responsible for the overall staffing coordination of patient visits including but not limited to, maintaining accurate and update to date patient schedules within EMR and scheduling systems. Staffing coordination duties also include the accurate and timely communication of scheduling chan

Expectations and Primary Responsibilities Buyer planner will collaborate cross-functionally with production and finance to schedule and prepare jobs to meet the demand of customers request date and purchase the associated materials/products. This responsibility entails planning future material/product demand, reviewing ERP system transactions, inventory levels, and backlog. Responsibilities · Schedule usage of production materials to ensure optimal production levels · Monitor material supply flow and identify any shortages or bottlenecks · Manage ship commits based on customer need date · Help manage and maintains the production schedule, shop floor level loading and coordination of material acquisition. · Generate capacity, on-time delivery, and production status reports in support of management team · Basic understanding of part / assembly drawings · Determines material requirement from master schedule · Place, track and expedite purchase orders, negotiate pricing, analyze data and m

About us: Based in Berkeley, CA, UPSIDE Foods grows meat, poultry, and seafood directly from real animal cells. These products are not vegan or vegetarian-they are delicious meat, made without the need to raise and slaughter billions of animals. In doing so, the company aims to address some of the most pressing environmental, animal welfare, and public health challenges, while still giving people the meat they love. Founded as the world's first cultivated meat company in 2015, UPSIDE Foods (formerly Memphis Meats) has achieved numerous industry-defining milestones, including being the first company to produce multiple species of meat (beef, chicken, and duck) and to sell a cultivated meat product in the United States. The company believes that people shouldn't have to choose between the foods they love and a thriving planet, and is working to build a better food system with access to delicious, humane, and sustainable meat, poultry, and seafood. UPSIDE Foods has won various industry aw

Overview: The ERP Functional Lead (Lead) will be responsible for transforming and standardizing business processes of production planning (PP) and manufacuring (MFG) to the new SAP implementation scope. This role will be part of a team that is responsible for providing subject matter expertise , strong analytics, and process development to optimize and deploy a common ERP strategy. As part of a Global cross-functional core team, this position will work with all divisional locations to design and implement standardized, best practice business solutions that leverage common processes, systems and data. The Lead has to be a good communicator. They will be in constant communication with the ERP core team (other Functional Leads), implementing team, Technical consultant and their project leader. Written communication skill is required for the purpose of e-mail to different groups, documentation related to Project, and reports generation. Responsibilities: In this role, the individual will b

It's fun to work in a company where people truly BELIEVE in what they're doing! We're committed to bringing passion and customer focus to the business. If you like wild growth and working with happy, enthusiastic over-achievers, you'll enjoy your career with us! Responsibilities Oversees activities related to Planning demand/supply, schedules, coordinates, and monitors final approval of products through the complete manufacturing cycle. Works from Monthly Approval Start plans to establish production schedules (associated with labor and capacity requirements) Coordinates production plans to ensure materials are delivered according to schedules. Provides input to management, schedules, and/or interfaces with marketing, sales, production, and engineering managers. Works to resolve (in case of design or schedule changes) labor and material shortages, backlogs, and other potential schedule interruptions. Oversees the master schedules and ensures comprehensive compliance with materials requi

Job Description: Shift Hours: 6-4:30 PM PST+ OT as needed. Responsible for the final quality audit before shipment of systems, upgrades, and miscellaneous ship kits. Collaborate closely with Manufacturing, Manufacturing Engineering, Master Scheduling, Production Control, Material handlers, Dock personnel and Packing contractors to ensure audits and quality inspections are completed so that products ship on time. Demonstrate proficiency with SAP SW as well as the MS Office suite. Clear communication and strong collaborative skills Persevere against challenging and time constrained issues. Inventing creative solutions to problems to ensure the job gets done on time. Provide constructive process improvement recommendations. Redline procedures as appropriate. Assist in the training and development of new hires. Support other product lines in plant clearance activities when necessary. Responsibilities: Auditing material against BOMs. Evaluating the quality of packaging. Visual spot check of

Job Description Job Description Company Description Crystal Bio Solutions, a member of Crystal Pharmatech, is a leading biologics analytical organization with operations in the San Francisco Bay Area and New Jersey. We specialize in bioanalytical and CMC analytical services for biotech and pharmaceutical companies developing biologics. Our expertise spans a wide range of therapeutic modalities, supporting projects from discovery through clinical development. Role Description Reporting directly to the CEO, the Director of Quality Assurance (QA) will be responsible for the development, management, and continuous improvement of quality systems ensuring compliance with Good Laboratory Practice (GLP), Good Clinical Laboratory Practice (GCLP), and other applicable regulatory standards for our bioanalytical GLP lab in Pleasanton, California. This role ensures that facilities, equipment, personnel, and procedures meet all regulatory requirements and effectively supports nonclinical and clinica

Description We are accepting applications for the 2025-26 school year for Aspire Golden State College Prep in Oakland. About Aspire: Aspire Public Schools operates a network of high-performing, college preparatory charter schools serving TK-12 scholars in communities across California. Founded in 1998-in an effort to transform the inequitable racial, social, and gender outcomes that our communities persist through-Aspire is one of the largest and most forward-thinking open-enrollment public charter school systems in the nation. Our purpose is to prepare our scholars for success in college, career, and life. At Aspire, we set a foundation for our scholars to gain knowledge, skills, and power to access and make choices for their families and post-secondary lives. Every day, our community of students, families, teachers and staff comes together to learn, work, and play in an environment grounded in our values of Bienestar (Well-Being), Culture of Belonging, Community Partnership, Agency &