JT580 - SUPPLY CHAIN MANAGER in Juncos at Quality Consulting Group

QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you’ll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA.

Responsibilities:

• Provides Supply Chain work group supervision and technical expertise in support of successfully completing daily operations within scope of responsibility.
• Provide meeting support to several cross-functional teams. Set project timelines and priorities based on project objectives and ongoing assignments.
• Create, analyze, and present metrics. Work closely with Supply Chain Operations and Planning teams to ensure product and material requirements are managed.
• Tracks and reports on spend to budget. Provides input to management for cost reduction opportunities.
• Comply with safety guidelines, cGMPs and other applicable regulatory requirements.
• May participate in area investigations/ audits.
• Maintain training proficiency.
• Initiate and/or implement changes in controlled documents.
• Participate in audits, initiatives and projects that may be departmental or organizational in scope.
• Initiate and complete routine investigation and technical tasks.
• Ensures all work is completed with minimal disruption and in compliance with all cGMP guidelines and Amgen 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.
• 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 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.

Qualifications:

• Bachelor’s degree in Life Sciences, Engineering, or related field.
• 4 years of directly related experience
• Must have well developed skills from Supervisor I
• Proficient in SAP
• Proficient in Excel, Word, Power Point, Smartsheet and other analytics software
• Knowledge documenting SOPs, deviations and/or CAPA records
• Veeva and SOP Management experience
• Fluent in English and Spanish
• Availability to support non-standard shift operation and extended hours
• Ability to adapt to multiple and increasing responsibilities, priorities, tasks, and projects simultaneously.
• 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.