- $100,000–$130,000 Per Year
- Full-time
li>Specific Process Ownership:responsible for implementation and maintenance of internal quality systems that support our business, including, but not limited to:
Our employees make the difference and we are committed to offering exceptional benefits and perks!
li>Specific Process Ownership:responsible for implementation and maintenance of internal quality systems that support our business, including, but not limited to:

As an Associate Category Manager at Uline, you'll own your product line, manage vendor relationships and guide a team of Product Management Analysts. Explore Uline.jobs to learn more!

As a Category Manager at Uline, you'll shape product strategy, build key vendor partnerships and guide a high-performing team – all while making a direct impact on our success. Explore Uline.jobs to learn more!
In this position, the manager will oversee the continued development and management of the company's Quality Management System while actively supporting and driving problem-solving initiatives related to quality issues. Our client is a leading manufacturer of electrical assemblies and fixtures, supplying products primarily to commercial and residential sectors, including offices, hotels, and restaurants.

div> Manage the day-to-day operations of a specified warehouse department, such as UPS, Freight, Returns, Receiving, Restock or Transfers. As a Warehouse Department Manager, you’ll support operations across Uline’s bright, clean and safe Kenosha facility, spanning across 800,000 square-feet. Explore Uline.jobs to learn more! Uline, a family-owned company, is North America’s leading distributor of shipping, industrial, and packaging materials with over 9,800 employees across 14 locations. div> Manage and develop a team of software architects responsible for creating and supporting architectures. Our employees make the difference and we are committed to offering exceptional benefits and perks! Provide technical support to Consumer Care by assisting with responses to customer inquiries related to product efficacy, usage, and concerns, and develop accurate science-based guidance and leverage consumer feedback to inform continuous improvement, quality enhancements, and future product innovation. Central is home to a diversified portfolio of market-leading brands, including Amdro, Aqueon, Best Bully Sticks, Cadet, C&S, Farnam, Ferry-Morse, Kaytee, Nylabone, Pennington, Sevin, and Zocon. Key Requirements: Oversee and manage the execution of [solidcore] continued education coach training (Levels 1-5) and supplemental educational workshops. Support team members and cross-functional partners execute Level and supplemental workshops virtually and in person. This role will lead complex new product development and customer-driven engineering projects from concept through production launch while coordinating cross-functional teams across engineering, manufacturing, quality, sales, and leadership. p>Reporting to the Director of Product Development, the Project Engineering Manager (Product Development) is responsible for managing the design and development of automotive transmission filtration solutions and will be principally located at the Des Plaines, IL facility. Our product line features a full line of high efficiency motors for industrial applications in water treatment, mining, oil and gas, and power generation, and for commercial applications such as pool and spa, condensers, cooling towers and large refrigeration units. This role bridges strategy and execution, serving as a primary electronics procurement partner to Engineering, R&D, Product Management, and Supplier Quality to ensure supplier readiness, cost competitiveness, and material availability for new product introductions. p>The Director of Partnership and Program Management is accountable for leading the global team of program and partnership managers who co-lead cross functional teams focused on the development of drug-device combination products and medical devices. This includes establishing an effective and efficient governance process, such as defining key interfaces, establishing meeting cadences, performance monitoring, project scope/change control, issue escalation, risk management, and financial tracking. The amount and availability of any bonus, commission,incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Companys sole and absolute discretion unless anduntil paid and may be modified at the Company's sole and absolute discretion, consistent with applicable law. While program managers own timeline management, provide technical leadership and granular program insights to identify acceleration opportunities, develop contingency strategies, and enable informed decision-making across the development lifecycle. Leads Chemistry, Manufacturing and Controls (CMC) teams and Product Presentation and Device Strategy Teams (PPDST) of functional representatives from various departments and divisions for projects involving external collaboration partners per Pipeline Commercialization Model (PCM). Preclinical Toxicology/Biological Sciences and Quantitative, Translational and Analytical Sciences (QTAS)/ADME (adsorption, distribution, metabolism and excretion) to ensure key deliverables for asset advancement are met and risks and mitigation plans are in place. Through comprehensive benefits (https://www.wesco.com/us/en/our-company/careers/work-at-wesco.html#benefits) and active community engagement, we create an environment where every team member has the opportunity to thrive. + Responsible for retaining and expanding existing company relationships, product lines or market segments, and soliciting new business from prospective customers and suppliers. p>Biologics Drug Product Development (Bio DPD), a part of Development Sciences within AbbVie's R&D, is a global organization that is responsible for drug product formulation and process development, and definition of the product presentation for biologics (proteins, conjugates, peptides, neurotoxins etc.) and genetic medicine (AAV, LNPs, Cell Therapy). This position will be an integral part of the product development and CMC teams and will have strong collaborations with several stakeholders, including discovery research, analytical research and development, bioprocess development, combination products development, product development science and technology, pilot plants and third-party manufacturers. Work closely with internal Ohio Medical functions (Sales, Marketing, Quality, Regulatory, Production, and Purchasing) to provide technical expertise, develop design solutions, and introduce new products and product enhancements that meet customer business regulatory requirements. Lead product development from concept through various stages of prototyping to final design by applying sound engineering principles including identification of product requirements, concept design and selection, prototyping, testing, etc. Assumptions of the business cases data collection: revenues, volumes expected, capital investments, product contents, quality, logistic costs, pricing, AMS impact Financial analysis of new product programs finalization consistently with the Strategic Business Plan assumptions Develop, monitor and report the financial impacts of product programs (budget preparation, ROI analysis, cash flow) presenting the financial evaluation results Tracking the financial results during the life of the program (program review) supporting the Platform in maintaining the target committed Ensures the mutual commitment and validation of the program financial targets with relevant Finance counterparts Control & approve the release of funds corresponding with the spending requests New Product cost tracking and deviation analysis Technical cost reduction and design changes impact on current product cost Capital appropriation request tracking in relation to the expected results Coordinate annual budget/forecast investment spending plans, analyzing trends and variances Support the allocation of R&D/Capex spending to the proper Project (WT) and the analysis of BDG/Fore/SBP planning activities Support the Software capitalization/depreciation process in coordination with finance accounting team and input from business department May include some general ledger maintenance, asset accounting, check, draft and analyze financial information and prepare financial reports and accounting statements, regulatory reports and filings, relationships with external consultants and advisors (e.g., accounting firms) Develop and enhance reporting tools, including Power BI dashboards mainly used to track FTE and Working Hours allocation by Project (WT) Experience Required. We use the following session cookies, which are all required to enable the website to function:"route" is used for session stickiness"careerSiteCompanyId" is used to send the request to the correct data center"JSESSIONID" is placed on the visitor's device during the session so the server can identify the visitor"Load balancer cookie" (actual cookie name may vary) prevents a visitor from bouncing from one instance to another. Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical information about the right treatments for the right patients, at the right time. p>Bachelor's degree in Food Science, Food Engineering, Chemistry, Chemical Engineering, Biological Engineering, or a related scientific field. Partner closely with Marketing, Operations, Quality, Procurement, and Account Management to define project scope and timelines. Biologics Drug Product Development (Bio DPD), a part of Development Sciences within AbbVie's R&D, is a global organization that is responsible for drug product formulation and process development, and definition of the product presentation for biologics (proteins, conjugates, peptides, neurotoxins etc.) and genetic medicine (AAV, LNPs, Cell Therapy). This position will be an integral part of the product development and CMC teams and will have strong collaborations with several stakeholders, including discovery research, analytical research and development, bioprocess development, combination products development, product development science and technology, pilot plants and third-party manufacturers. Biologics Drug Product Development (Bio DPD), a part of Development Sciences within AbbVie's R&D, is a global organization that is responsible for drug product formulation and process development, and definition of the product presentation for biologics (proteins, conjugates, peptides, neurotoxins etc.) and genetic medicine (AAV, LNPs, Cell Therapy). This position will be an integral part of the product development and CMC teams and will have strong collaborations with several stakeholders, including discovery research, analytical research and development, bioprocess development, combination products development, product development science and technology, pilot plants and third-party manufacturers. Description: Biologics Drug Product Development (Bio DPD), a part of Development Sciences within AbbVie's R&D, is a global organization that is responsible for drug product formulation and process development, and definition of the product presentation for biologics (proteins, conjugates, peptides, neurotoxins etc.) and genetic medicine (AAV, LNPs, Cell Therapy). This position will be an integral part of the product development and CMC teams and will have strong collaborations with several stakeholders, including discovery research, analytical research and development, bioprocess development, combination products development, product development science and technology, pilot plants and third-party manufacturers.


