Production Lead Salary at Farmlandfoods BETA

Manufacturing Product Lead Position Summary Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments for patients annually. Catalent's Kansas City facility is home to our Oral & Specialty Drug Delivery, Biologics Analytical Services and Clinical

Company Overview: COME JOIN OUR JOURNEY! When you join TT, you join our global community of visionaries, creators, and achievers dedicated to solving technology challenges for a sustainable world. Simply put, we are a global manufacturer with a passion for engineering advanced electronics that benefit our planet and people for future generations. We are committed to having a positive impact on the world through a culture built around safety, transparency, collaboration, and positive relationships. Our teams are fueled by performance and expertise, leading the charge in innovation, efficiency and delivering world-class customer service. Be part of the journey. Role Overview and Responsibilities: This position requires use of information which is subject to the International Traffic in Arms Regulations (ITAR). All applicants must be U.S. persons within the meaning of ITAR. ITAR defines a U.S. person as a U.S. Citizen, U.S. Permanent Resident (i.e. 'Green Card Holder'), Political Asylee,

Must-Have Qualifications: Bachelor’s degree in electrical engineering 6+ years of experience as an engineer with substations or switchyards Technical knowledge of relays, protections and controls for substations/switchyards Experience creating grounding, area class, power, single line, schematic and motor control drawings Ability to specify high, medium, and low voltage electrical equipment (Breakers, Transformers, Switchgear, etc.) Qualification Plusses: PE (Professional Engineer) Able to perform engineering calculations, e.g., load flow, short circuit, arc flash, harmonics, equipment sizing, large motor starting, grounding, transient stability, electromagnetic transients, insulation coordination, etc. Day-to-Day: A leading energy client of Insight Global is seeking a Lead Protection Engineer to join their engineering team in Leawood, KS. We are looking for an individual who is passionate about ownership and quality. This role involves leading technical work on EPC projects. Reporting

Company Overview: COME JOIN OUR JOURNEY! When you join TT, you join our global community of visionaries, creators, and achievers dedicated to solving technology challenges for a sustainable world. Simply put, we are a global manufacturer with a passion for engineering advanced electronics that benefit our planet and people for future generations. We are committed to having a positive impact on the world through a culture built around safety, transparency, collaboration, and positive relationships. Our teams are fueled by performance and expertise, leading the charge in innovation, efficiency and delivering world-class customer service. Be part of the journey. Role Overview and Responsibilities: This position requires use of information which is subject to the International Traffic in Arms Regulations (ITAR). All applicants must be U.S. persons within the meaning of ITAR. ITAR defines a U.S. person as a U.S. Citizen, U.S. Permanent Resident (ie, "Green Card Holder"), Political Asylee, o

Senior Data Scientist, Molecular Modeling and Drug Discovery (Specialist Senior) - SFL Scientific SFL Scientific, a Deloitte Business practice brings together several key capabilities to architect integrated programs that transform our clients' businesses, including Business Strategy, Environmental, Social and Governance Strategy, Technology Strategy & Business Transformation, and AI & Data Strategy. Professionals will serve as trusted advisors to our clients, working with them to make clear data-driven choices about where to play and how to win - ultimately driving growth and enterprise value. We are hiring a Senior Data Scientist with technical and scientific expertise in AI-based drug discovery and molecular modeling to support our team in working with clients, organizing multi-project development, and enabling technical solution delivery. Join a rapidly growing team of professionals working to build a world-class data science practice with a focus on solving complex R&D problems. R

Join the team at Heartland Coca-Cola Bottling Company! Job Summary The Manufacturing Training Manager is responsible for the learning programs and employee development for all of production and the production warehouse teams. Also responsible for working with subject matter experts and leaders to design and implementation of training content and programs to ensure that the needs of the manufacturing employees and departments are met. Job Responsibilities Analyze, identify, prepare, and deliver a broad range of training, using a variety of training methods and training materials for the manufacturing and warehouse teams to ensure enhanced performance. Leveraging vendor partners and internal SMEs to ensure training programs are current and accurate. Collect feedback on training and make necessary recommendations to ensure constant improvement of training programs, while collaborating with leadership on gap analysis/assessments to ensure that training content and programs are updated base

**Quality Specialist II, Supplier and Material Management** **Position Summary:** Catalent is a global, high-growth, public company and a leading partner for the pharmaceutical industry in the development and manufacturing of new treatments for patients worldwide. Your talents, ideas, and passion are essential to our mission: to help people live better, healthier lives. Catalents Kansas City facility is home to our Oral & Specialty Drug Delivery, Biologics Analytical Services and Clinical Supply Services businesses. The site provides a range of integrated services for oral solid dosage forms, from formulation development and analytical testing to clinical and commercial-scale manufacture. The Kansas City facility is a Center-of-Excellence for our Biologics Analytical Services business. Our talented team has over 25 years of experience providing analytical services for stand-alone and integrated biologics projects. Catalent Pharma Solutions in Kansas City, MO is hiring a Quality Special

Job Type: Staff Job Description: The Quality Improvement (QI) and Research Specialist supports Kansas City University's (KCU) GME community by fostering a culture of continuous quality improvement, patient safety, and scholarly activity. The specialist collaborates with residents, fellows, faculty, and institutional leaders to implement QI initiatives, enhance research opportunities, and ensure compliance with ACGME standards, including Clinical Learning Environment Review (CLER) requirements. Essential Functions & Responsibilities: Develop, implement, and oversee QI/PS initiatives across GME programs Teach QI and PS concepts to residents, fellows, and faculty Maintain a centralized catalog of QI projects and outcomes Conduct audits, analyze data, and collaborate with the DIO on improvements Lead meetings with clinical site QI and risk management staff Manage data collection, analysis, and reporting for ACGME CLER focus areas Collaborate with program directors and clinical sites on com