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Director of Supply Chain - PENNSYLVANIA - USA

Salary undisclosed

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Director of Supply Chain

  • Pennsylvania, USA (you must have US nationality and already live in the USA)
  • In-office (not remote)
  • Salary: $135k - $160k
  • Travel: 25%

Join a dynamic team revolutionizing biopharmaceutical manufacturing industry! As Director of Supply Chain, you will report to the COO and lead a talented team overseeing procurement, inventory, international shipping, and

logistics. you will need proven managerial experience and a knack for navigating operational, tactical, and strategic facets of a global supply chain, and liaising between clients and suppliers.

Key Responsibilities

  • Provide strong leadership to a team of supply chain professionals, fostering growth and efficiency.
  • Oversee supply planning for all projects, ensuring target inventory levels and customer service metrics.
  • Optimize flow of goods using lean principles and strategic segmentation.
  • Collaborate cross-functionally to launch new products on time, integrating consumer needs and supplier insights.
  • Coordinate supply chain reporting and track KPIs to maximize operational efficiency.
  • Build resilient and innovative manufacturing networks.
  • Identify and implement process improvements to hedge against cost, material, and demand volatility.
  • Lead meetings and training to enhance productivity and meet business objectives.
  • Support acquisition and divestiture activities.
  • Manage reporting and budgeting initiatives.

Qualifications:

  • Bachelor’s Degree in Supply Chain or related field (MBA preferred) with 8+ years in pharma, life sciences, or capital equipment and 5+ years in leadership
  • Certified Supply Chain Professional (CSCP) preferred
  • Strong leadership, communication, and influencing skills
  • Expertise in supplier relationship management, strategic sourcing, spend analysis, contract lifecycle management, and budget planning.
  • Proven ability to reduce costs, streamline operations, and develop strategic relationships
  • Proficiency in Microsoft Office and master production scheduling; Syteline experience a plus
  • Knowledge of regulatory requirements, FDA ISO-9000, and project management.

Seize this opportunity to drive growth and innovation in a leading biopharmaceutical manufacturing company!