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Manager, Supply Chain Jobs

Company

Enzyvant

Address Cary, NC, United States
Employment type FULL_TIME
Salary
Category Biotechnology Research
Expires 2023-06-16
Posted at 1 year ago
Job Description
Who We Are
Enzyvant is a biopharmaceutical company making life-altering impact for people affected by rare disease, where the communities are small, and the human need is immense. Driven by purpose, we engage with rare disease communities with compassion and commitment, partnering to accelerate the development of transformative medicines they so urgently need. We prioritize collaborative connections with academia, industry, associations, advocacy groups and government, because strong relationships make bold science possible. 
A nimble and unique organization, Enzyvant has a full range of capabilities spanning non-clinical and clinical development and commercialization and is developing in-house manufacturing. Enzyvant has delivered a first-of-its-kind FDA approval in regenerative medicine and promising advances against some of the greatest challenges in immunology and cardiopulmonology. Enzyvant is part of Sumitovant, wholly owned by Sumitomo Pharma
At Enzyvant, our experts are thoughtful, experienced, and passionate about solving some of the greatest challenges in rare diseases today. We believe that through steady focus and determination, we will continue to accomplish great things for the rare disease community.
By joining the Enzyvant team, you’ll become a fundamental part of the development and growth of a nimble and unique organization. Our range of capabilities relies on the skills of experts in development, commercialization, and manufacturing.
For more information about Enzyvant, visit www.Enzyvant.com.
Description
Enzyvant is seeking an experienced and motivated Manager of Supply Chain to join our growing organization. Reporting to the Associate Director of Supply Chain & Procurement, this critical position will interface with a diverse team across the various external vendors that are producing Rodatristat. We are looking for a professional who has extensive experience in the biotech/pharmaceutical industry, and who has specific experience in external supply chain, vendor relationships management, and Phase 2b/3 clinical trial material management.
Responsibilities
  • Work alongside the Rodatristat internal team (including clinical and non-clinical) and external vendors to ensure appropriate inventory of materials to support clinical and nonclinical operations.
  • This position will need to be able to support labeling, packaging, and distribution of GXP late-stage assets from clinical to commercial.
  • Calls and meetings might happen before or after normal hours based on the location of the external manufactures.
  • Lead key internal operations including external manufacturing through facilitation of contracts, vendor relations and audits.
  • Drive knowledge management activities including documentation of meeting minutes and action items during internal and external alignment team meetings and tracking performance metrics from critical supply and service vendors
  • Establish and maintain detailed supply strategy for a Phase 2b/3 supply of our critical material.
  • Establish and foster strong collaborative relationships with current vendor partners and service providers.
  • Assure alignment of inventory and supply of critical materials with the manufacturing schedule and forecast for all Enzyvant products.
  • Work alongside Quality to ensure newly proposed vendors have undergone due diligence and new and existing vendors have the appropriate level of oversight and documentation, including new and annual on-site Quality audits and Quality Agreements in place
  • This position will need to work cross functionally with Rodatristat ethyl and clinical teams.
Qualifications
  • Experience and strong understanding of GMP and CDMO Pharmaceutical Development.
  • Strong knowledge of Procurement, Supply Chain, Logistics
  • Experience interacting, managing, and resolving issues with vendors across the world
  • APICS CSCP/CPIM certification is a plus
  • GMP Purchasing and regulations
  • 5+ years of industry experience with BS/BA or 4+ years of industry experience
  • Excellent negotiation, organizational, interpersonal, and problem-solving skills.
Skills
  • Proven ability to manage multiple projects, identify and resolve issues.
  • Experience in building teams
  • Build strong, open, and collaborative working relationships with both internal and external stakeholders
  • Broad experience in a small company environment is a plus
  • Experience with pharmaceutical supply chain intricacies
Enzyvant values an inclusive and diverse workforce and provides equal employment opportunity for all applicants and employees. As such, Enzyvant prohibits discrimination and harassment of any type with regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. This policy applies to all terms and conditions of employment.