58 Amerisourcebergen jobs in Conshohocken

Join Our Team!Position: Supply Chain AnalystLocation: Pennsauken, NJPay Rate: $20/hrAre you ready to take the next step in your career? We're actively seeking a dynamic and motivated Supply Chain Analyst to join our team in Pennsauken, NJ! This is a fantastic opportunity to work with an award-winning organization that values equality, diversity, and family.Job Description:Support purchasing, production, and accounting teams by managing vendor communication, analyzing inventory data, and processing job and sales orders efficiently. Job Responsibilities:Analyze vendor lead times, pricing, and inventory discrepancies to support procurement and cost control.Maintain vendor relationships and follow up on open orders, back orders, and quality concerns.Review and update job release files and support sales order processing in QuickBooks and cERP.Collect data on operations to improve procurement efficiency and supplier performance.Support accounting and production teams with billing questions and coordination needs. Shift/Hours:7am-3:30pmJob RequirementsBachelor's degree in supply chain, operations or business management or equivalent experienceMinimum 7 years work experience in Procurement and Supplier ManagementIntermediate PC skills - Excel, Outlook, WordWorking knowledge of ERP systemsReady to make a move? Contact us today!ACCU Pennsauken Job Center6000 NJ-38Pennsauken, NJ 08109Phone: 856-662-2727Email: Why ACCU Staffing? Join an award-winning organization that takes pride in being South Jersey/Philadelphia's top staffing company! As an equal opportunity, family, and women-owned employer, we offer a supportive and inclusive work environment.Benefits at ACCU Staffing include:Medical insurance Paid time offReferral bonusesRapid-pay debit card for immediate access to your paycheck!Don't miss out on this incredible opportunity! Take the first step toward a rewarding career with ACCU Staffing. Apply now and be a part of our success story!

Supply Chain Analyst | Tech Ops Supply Chain | Hatfield | Hybrid (2 days office) About us:Ocado Technology is putting the world's retailers online using the cloud, robotics, AI, and IoT. We develop the innovative software and systems that power Ocado.com, the world's largest online-only grocery retailer as well as the global 'Ocado Smart Platform'. With everything from websites to fully autonomous warehouses that we design in-house, our employees need to be specialists in a wide range of technologies to help drive our business. We champion a value-led culture to get our teams working at their very best and to help create a collaborative working environment that our people love. About the role: The Supply Chain Analyst is core to the data-driven decision making philosophy in Supply Chain, and has the responsibility of developing and improving tools & reports whilst ensuring the appropriate level of support is available for all projects. The Analyst ensures that their products are developed and maintained to meet the evolving needs of stakeholders to ensure accuracy and relevance, as well as facilitating efficiencies in supported workflows. We go beyond technology, we facilitate outcomes. You will need a passion for digging down to the root and driving sustainable change and improvement. The ability to appreciate Supply Chain from end to end and keep a focus on the impacts your efforts bring in that broad picture will help you succeed.In this job, you will be accountable for:Providing analytical support; daily, weekly and monthly key performance indicator reporting Providing insights for Supply Chain teams and the senior leadership teams which are clear, unambiguous and actionable, and underpin a positive impact to business performanceCoordinating root cause analysis cases that arise from these insightsMaintaining and enhancing tools and services to ensure they deliver efficiencyDevelop and maintain an understanding of what data is involved where in Supply Chain with the aim of being able to deliver data-centric expert opinion to all relevant areas and projects.What we're looking for:Working knowledge of SQLAbility to work with Data Visualisation Tools (Looker Studio preferred) Proficient with Google Suite (Microsoft Office is an acceptable alternative).Strong communication skills (able to present in a variety of formats and styles to a range of technical and non-technical stakeholders)Commercially aware and consider the cost and operational impacts of decisions and proposalsA healthy degree of curiosity with a good capacity for abstract and critical thinking.We'd also love to hear from you if you have;Knowledge of Google script or VBAKnowledge of Oracle Fusion and/or Oracle ApexKnowledge of Python.Knowledge of Enterprise tools including Jira What do I get in return:30 Day 'work from anywhere' policy Remote working for the month of August25 days annual leave, rising to 27 days after 5 years service (plus optional holiday purchase)Pension scheme (various options available including employer contribution matching up to 7%)Private Medical Insurance22 weeks paid maternity leave and 6 weeks paid paternity leave (once relevant service requirements complete)Train Ticket loan (interest-free)Cycle to Work SchemeOpportunity to participate in Share save and Buy as You Earn share schemes15% discount on Ocado.com and free delivery for all employeesIncome Protection(can be up to 50% of salary for 3 years) and Life Assurance(3 x annual salary)#LI-HYBRID#LI-OT#LI-JT1

For over 100 years, Lasko Products has been a market leader in delivering innovative home comfort solutions. We are seeking a dynamic, results-oriented Supply Chain Manager to join our team at our headquarters in West Chester, PA. As the Supply Chain Manager, you will support the end-to-end supply chain. You will collaborate across multiple departments and drive the execution of strategic initiatives to ensure the seamless flow of goods and materials. Your expertise will contribute to maintaining Lasko's industry-leading position while optimizing processes for greater efficiency, cost-effectiveness, and performance. This role will report to the Director of Supply Chain. Key Responsibilities: Sales Forecast & Purchase Order Management: Oversee the sales forecast, purchase orders, and supplier contract negotiations for specific product lines to ensure alignment with business goals and market demand. International Procurement & Supplier Management: Develop and maintain strong relationships with global suppliers, ensuring compliance with quality standards, contract terms, and cost-effectiveness. Shipment & Container Tracking: Manage tracking and follow-ups on international shipments, resolving delays and ensuring smooth transit. Process Integration: Support the integration of suppliers, freight, logistics, and customer service into Lasko's organizational processes to drive operational efficiency and smooth collaboration across teams. Inventory & Stocking Strategy: Support the development and execution of product stocking plan for North America, including inventory levels, lead times, and weather event related stock, ensuring product availability to meet Sales & Operations requirements. Import & Logistics Oversight: Manage the ordering, receipt, coding, and classification of imported components and finished goods, utilizing LP Vision systems to forecast and optimize imported product flows. Drive warehouse consolidation and optimization initiatives across Lasko's network. Seasonal Readiness: Work closely with the Far East team, Engineering, and Sales to ensure the supply chain is ready for seasonal production runs, new product launches, and direct shipments. Procure to Pay Process Management: Collaborate with Finance to assist with Procure to Pay process, ensuring seamless procurement, invoicing, and payment operations Expedited Freight Management - Proactively minimize expedited freight by implementing strategic planning, root cause analysis, and process improvements. Develop and execute mitigation strategies to reduce costs, improve forecasting, and enhance supply chain efficiency. Track and report key metrics to drive continuous improvement and accountability. What You'll Bring to the Table: Expertise in Supply Chain & Logistics: A deep understanding of supply chain management, import/export processes, and logistics optimization, with a track record of driving efficiency and cost savings. Collaborative Leadership: Strong ability to lead cross-functional teams and work effectively with internal and external stakeholders, including suppliers, engineering, sales, and IT. Project Management Skills: Proven experience in managing large, complex projects with the ability to execute them successfully within deadlines. Strategic Thinking: A keen eye for identifying cost improvement opportunities and optimizing processes to meet business objectives. Global Supply Chain Knowledge: Experience in managing international shipments, understanding of FTZ procedures, and familiarity with compliance and regulatory requirements for global trade. Required Education and Experience Bachelor's degree in Business, Finance, Engineering or related discipline 5+ years of Manufacturing/ Business experience which includes International Suppliers Industry experience with Retail customers ( traditional brick-and-mortar and online) Seasonal business experience 3+ years of direct supervisory experience About Lasko Products Better Air Starts Here. Lasko Products is the leading air solutions brand with a reputation for reliable products, peak performance, and perpetual innovation - our commitment to our customers for over a century. Founded in 1906 by Henry Lasko in Philadelphia, Lasko has evolved for over a century to become the global leader in air solution products. From our roots in small appliances, fans, and portable heaters, we've grown to become the leading home comfort company while maintaining our unwavering commitment to quality and value. Today, Lasko stands as a symbol of innovation, offering consumers around the world high-performance products; portable fans, heaters, air purifiers, humidifiers, and home ventilation solutions. Our well-known brands, such as B-Air, Air King, and Guardian Technologies, serve both consumer and commercial markets across North America and internationally. As an American company, we take pride in upholding the spirit of hard work, trust and accessibility, ensuring that Lasko remains available to all, for generations to come. Headquartered in West Chester, Pennsylvania, with manufacturing and distribution facilities nationwide, Lasko continues to set the standard in the air solutions category for another 100 years. Lasko's mission is to enhance lives by creating comfortable environments with innovative products you can trust. The company's success is based on Five Core Values: Be Bold Challenge the status quo Courageously pursue the impossible Reject mediocrity Be Together Work together for success Drive trust and candor with each other Prioritize "We" before "I" Be A Leader Lead with personal conviction Inspire each other to deliver high- quality results Leverage resilience and agility to drive excellence Be Accountable Consistently deliver to our customers Embrace commitments as a contract Take pride in our actions Be The Change Demonstrate a passion to win Make a difference at work in our communities Step forward and take initiative Why Join Lasko? At Lasko, we believe people do their best work when they're supportedpersonally and professionally. That's why we offer flexible hours and a hybrid work schedule for our corporate team, promoting employees to balance life and work in a way that fits their lifestyle. Our dog-friendly corporate headquarters adds a fun, welcoming atmosphere, while our competitive salaries with bonus potential recognize and reward your contributions. We also offer a comprehensive benefits package that includes a strong 401(k) match, wellness incentives, and robust health coverage. Join Lasko and be part of a legacy of innovation - at a company that values flexibility, growth, and a culture where you can thrive.

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our 35,000 employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world.

Position Overview:

The Associate Director, Supply Chain will lead and grow a supply chain team responsible for ensuring supply continuity of all critical components and consumables required for the uninterrupted manufacturing of commercial and clinical radiopharmaceutical drug products across a worldwide network of cGMP manufacturing sites. Key focus areas include optimizing the global supply chain, maintaining approved suppliers/products for global operations, demand/supply/capacity planning, sourcing, labeling, dispensing, inventory management, shipping, distribution, and selection of drug supply-related vendors and depots. The ideal candidate will have a deep understanding of supply chain networks, clinical regulations, global import/export requirements, commercial regulations, timelines, end-to-end planning, and analytics to facilitate communications across a variety of functions to deliver cost-effective supply chain solutions while balancing multiple business objectives. As head of the supply chain team, the ideal candidate must be highly detail-oriented, organized, results driven, and passionate about mentoring and developing direct reports to drive high performance in alignment with business goals.

This is a hybrid position requiring a minimum of three days per week on-site at the Philadelphia office.

Responsibilities:

• Ensure uninterrupted supply of critical components and consumables to meet global manufacturing needs for commercial and clinical products
• Regularly evaluate and communicate risks and interruptions to the supply chain and proactively establish mitigations wherever necessary
• Partner closely with Commercial, Clinical, Manufacturing, and Leadership teams to establish and maintain robust supply/demand forecasts in alignment with core business goals
• Build, deploy, and maintain tools for cross-functional tracking and communication of approved suppliers, products, and components
• Review technical and regulatory documentation to ensure accuracy, consistency, and currency of all critical components/key consumables
• Support management and closure of product investigations associated with critical components/key consumables including authoring and reviewing investigation documents and risk assessments
• Track component recalls/retrievals and communicate cross-functionally as necessary
• Identify alternative component sources; manage associated change control process where needed
• Manage financial planning and budget forecasting activities associated with the supply chain function; perform invoice reconciliation, ensure functional area adherence to budget
• Prepare and present supply chain updates at regular internal work group and team meetings; support the preparation of presentation materials for senior leadership, when required
• Assume additional responsibilities supporting the broader CMC Development group, as needed.

Basic Requirements:

• BS or MS degree in supply chain, science/engineering, production operations management, business, or related field with 5+ years of experience in a supply chain function within a pharmaceutical environment
• 2+ years of CMC experience in the biotechnology or pharmaceutical development industries
• Strong supply management experience/knowledge in forecasting, demand/supply planning, IRT systems, inventory management/ERP systems, clinical labeling, distribution including cold chain, import/export, reverse logistics, CMC and GxP regulations

Preferred Requirements:

• Supply Chain Management certification(s) (e.g., CSCP, CPIM, SCOR-P, CPM, etc.) are a plus
• Familiarity with cGMPs as well as US, European, Japanese, Chinese, and ICH regulations and industry standards for pharmaceutical manufacturing
• Experience within a CMC/cGMP role in the radiopharmaceutical industry
• Familiarity with collaborative project management tools such as Microsoft Project, Smartsheet, Monday, Jira, etc.
• Solid understanding of pharmaceutical manufacturing and release within a cGMP environment
• Excellent interpersonal, verbal, and written communication skills with the ability to work with uncertainty and to resolve conflict in a constructive manner
• Must be self-motivated and comfortable in a fast-paced, demanding and dynamic work environment
• Must be proficient in the Microsoft 365 environment

Additional Information:

• Lilly is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status
• Eli Lilly and Company, Lilly USA, LLC and our wholly owned subsidiaries (collectively "Lilly") are committed to help individuals with disabilities participate in the workforce and ensure equal opportunity to compete for jobs. If you are an individual with a disability and require a reasonable accommodation to participate in the application process, please email Lilly Recruiting Compliance.
• Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form for further assistance.
• Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.
• Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). Learn more about all of our groups.
• Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is $122,250 - $179,300. Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities). Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world.

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our 35,000 employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world.

Position Overview:

The Associate Director, Supply Chain will lead and grow a supply chain team responsible for ensuring supply continuity of all critical components and consumables required for the uninterrupted manufacturing of commercial and clinical radiopharmaceutical drug products across a worldwide network of cGMP manufacturing sites. Key focus areas include optimizing the global supply chain, maintaining approved suppliers/products for global operations, demand/supply/capacity planning, sourcing, labeling, dispensing, inventory management, shipping, distribution, and selection of drug supply-related vendors and depots. The ideal candidate will have a deep understanding of supply chain networks, clinical regulations, global import/export requirements, commercial regulations, timelines, end-to-end planning, and analytics to facilitate communications across a variety of functions to deliver cost-effective supply chain solutions while balancing multiple business objectives. As head of the supply chain team, the ideal candidate must be highly detail-oriented, organized, results driven, and passionate about mentoring and developing direct reports to drive high performance in alignment with business goals.

This is a hybrid position requiring a minimum of three days per week on-site at the Philadelphia office.

Responsibilities:

• Ensure uninterrupted supply of critical components and consumables to meet global manufacturing needs for commercial and clinical products
  
• Regularly evaluate and communicate risks and interruptions to the supply chain and proactively establish mitigations wherever necessary
  
• Partner closely with Commercial, Clinical, Manufacturing, and Leadership teams to establish and maintain robust supply/demand forecasts in alignment with core business goals
  
• Build, deploy, and maintain tools for cross-functional tracking and communication of approved suppliers, products, and components
  
• Review technical and regulatory documentation to ensure accuracy, consistency, and currency of all critical components/key consumables
  
• Support management and closure of product investigations associated with critical components/key consumables including authoring and reviewing investigation documents and risk assessments
  
• Track component recalls/retrievals and communicate cross-functionally as necessary
  
• Identify alternative component sources; manage associated change control process where needed
  
• Manage financial planning and budget forecasting activities associated with the supply chain function; perform invoice reconciliation, ensure functional area adherence to budget
  
• Prepare and present supply chain updates at regular internal work group and team meetings; support the preparation of presentation materials for senior leadership, when required.
  
• Assume additional responsibilities supporting the broader CMC Development group, as needed.
  

• BS or MS degree in supply chain, science/engineering, production operations management, business, or related field with 5+ years of experience in a supply chain function within a pharmaceutical environment
  
• 2+ years of CMC experience in the biotechnology or pharmaceutical development industries
  
• Strong supply management experience/knowledge in forecasting, demand/supply planning, IRT systems, inventory management/ERP systems, clinical labeling, distribution including cold chain, import/export, reverse logistics, CMC and GxP regulations
  

• Supply Chain Management certification(s) (e.g., CSCP, CPIM, SCOR-P, CPM, etc.) are a plus
  
• Familiarity with cGMPs as well as US, European, Japanese, Chinese, and ICH regulations and industry standards for pharmaceutical manufacturing
  
• Experience within a CMC/cGMP role in the radiopharmaceutical industry
  
• Familiarity with collaborative project management tools such as Microsoft Project, Smartsheet, Monday, Jira, etc.
  
• Solid understanding of pharmaceutical manufacturing and release within a cGMP environment
  
• Excellent interpersonal, verbal, and written communication skills with the ability to work with uncertainty and to resolve conflict in a constructive manner
  
• Must be self-motivated and comfortable in a fast-paced, demanding and dynamic work environment
  
• Must be proficient in the Microsoft 365 environment
  

• Lilly is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status
  
• Eli Lilly and Company, Lilly USA, LLC and our wholly owned subsidiaries (collectively "Lilly") are committed to help individuals with disabilities participate in the workforce and ensure equal opportunity to compete for jobs. If you are an individual with a disability and require a reasonable accommodation to participate in the application process, please email Lilly Recruiting Compliance. Please note, this email address is intended for use only to request a disability accommodation, please email Lilly Recruiting Compliance for further assistance. Inquiries which are not requests for accommodations may not receive a response.
  

• Ensure uninterrupted supply of critical components and consumables to meet global manufacturing needs for commercial and clinical products
• Regularly evaluate and communicate risks and interruptions to the supply chain and proactively establish mitigations wherever necessary
• Partner closely with Commercial, Clinical, Manufacturing, and Leadership teams to establish and maintain robust supply/demand forecasts in alignment with core business goals
• Build, deploy, and maintain tools for cross-functional tracking and communication of approved suppliers, products, and components
• Review technical and regulatory documentation to ensure accuracy, consistency, and currency of all critical components/key consumables
• Support management and closure of product investigations associated with critical components/key consumables including authoring and reviewing investigation documents and risk assessments
• Track component recalls/retrievals and communicate cross-functionally as necessary
• Identify alternative component sources; manage associated change control process where needed
• Manage financial planning and budget forecasting activities associated with the supply chain function; perform invoice reconciliation, ensure functional area adherence to budget
• Prepare and present supply chain updates at regular internal work group and team meetings; support the preparation of presentation materials for senior leadership, when required.
• Assume additional responsibilities supporting the broader CMC Development group, as needed.

• BS or MS degree in supply chain, science/engineering, production operations management, business, or related field with 5+ years of experience in a supply chain function within a pharmaceutical environment
• 2+ years of CMC experience in the biotechnology or pharmaceutical development industries
• Strong supply management experience/knowledge in forecasting, demand/supply planning, IRT systems, inventory management/ERP systems, clinical labeling, distribution including cold chain, import/export, reverse logistics, CMC and GxP regulations

• Supply Chain Management certification(s) (e.g., CSCP, CPIM, SCOR-P, CPM, etc.) are a plus
• Familiarity with cGMPs as well as US, European, Japanese, Chinese, and ICH regulations and industry standards for pharmaceutical manufacturing
• Experience within a CMC/cGMP role in the radiopharmaceutical industry
• Familiarity with collaborative project management tools such as Microsoft Project, Smartsheet, Monday, Jira, etc.
• Solid understanding of pharmaceutical manufacturing and release within a cGMP environment
• Excellent interpersonal, verbal, and written communication skills with the ability to work with uncertainty and to resolve conflict in a constructive manner
• Must be self-motivated and comfortable in a fast-paced, demanding and dynamic work environment
• Must be proficient in the Microsoft 365 environment

• Lilly is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status
• Eli Lilly and Company, Lilly USA, LLC and our wholly owned subsidiaries (collectively "Lilly") are committed to help individuals with disabilities participate in the workforce and ensure equal opportunity to compete for jobs. If you are an individual with a disability and require a reasonable accommodation to participate in the application process, please email Lilly Recruiting Compliance. Please note, this email address is intended for use only to request a disability accommodation, please email Lilly Recruiting Compliance for further assistance. Inquiries which are not requests for accommodations may not receive a response.