JT953 - SUPPLY CHAIN MANAGER

• Ensures all work is completed with minimal disruption and in compliance with all cGMP guidelines and client's procedures.
• Direct and coordinate daily activities of personnel responsible for material receipt, storage and transport.
• Ensures materials are received, stored and transported according to established performance standards and all applicable procedures and regulations.
• Interacts with internal and external regulatory agencies to ensure compliance with cGMP, DOT, OSHA requirements.
• Collaborate with other sites to maintain optimal flexibility for the storage of all materials and product.
• Identify and oversee implementation of new and improved business and compliance systems and tools.
• Partner with key internal customer groups and/or external suppliers to ensure successful operations and performance targets are achieved.
• Responsible for business continuity programs for assigned areas.
• Participate on global functional teams to coordinate and improve the transportation and Logistics of material movement and storage across the Client Supply Chain.
• Direct and coordinate daily activities of personnel responsible for developing and managing Product demand and forecasts.
• Organize and communicate on a regular basis the total demand and supply requirements to senior management.
• Coordinate the Master Production Schedule for Finished Goods and effectively communicate any impact created by, and to the supply plan.
• Manage the process of gathering, evaluating and feedback of global demand requirements.
• Provide and coordinate the development of business case scenarios that demonstrate the impact of current or proposed operations plans.
• Manage the preparation and communication of the Company wide Inventory Distribution Plan to achieve corporate goals of customer satisfaction and risk management.
• Develop and coordinate the long-range production requirements based on Marketing forecasts, product approval and release timelines, clinical requirements, SKU put-up information and business planning timelines estimates.

• Bachelor’s degree in Life Sciences, Engineering, or related field.
• Written and Verbal communication in English and Spanish
• In-depth experience in Root Cause Analysis (Fishbone, Six Boxes, Fishbone, 5 Why’s)
• Supply Chain experience (receiving, suppliers, warehouse, shipping)
• Strong Technical Writing Skills
• Skilled in performance of GMP operations
• Compliance/Regulatory knowledge and interaction experience
• Experience leading cross-functional teams for RCA and problem solving
• Ability to communicate and collaborate with technical and management staff within manufacturing, process development, supply chain, and quality.
• Strong presentation skills.
• Project management skills.
• Administrative Shift

Quality Consulting Group, LLC is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.