Jt607 - Supply Chain Manager

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:

• 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.
• Participate on global functional teams to coordinate and improve the transportation and Logistics of material movement and storage across the 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.
• 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.
• Provide meeting support to several cross-functional teams.
• Set project timelines and priorities based on project objectives and ongoing assignments.
• 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.
• Initiate and/or implement changes in controlled documents.
• Initiate and complete routine investigation and technical tasks.

Qualifications:

• Bachelor’s degree in required area
• +4 years of directly related experience
• Experience with spreadsheets and schedules
• Knowledgeable of Trackwise, SAP, EDW, Excel, Word, Power Point, Smartsheet and other analytics software.
• Knowledge documenting SOPs, deviations and/or CAPA records
• Trackwise, 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.