Director of Supply Chain
Everyday RobotsSalary not specified
Full Time
Mid-level (3 to 4 years), Senior (5 to 8 years)
Not SpecifiedCompensation
Expert & Leadership (9+ years)Experience Level
Full TimeJob Type
UnknownVisa
Biopharmaceutical, PharmaceuticalIndustries
Requirements
- 12+ years of relevant experience in related field and a BS or BA; or 10+ years of relevant experience and a MA/MBA
- Expert working knowledge of clinical supply chain best practices
- Experience working in a GxP environment
- Strong cross-functional, multi-cultural awareness and communication skills
- Able to develop complex concepts
Responsibilities
- Serves as the clinical supply lead on PDM sub-teams especially for complex development programs (e.g., late phase, acquisition, partnership/alliance, new modality, etc.)
- Leads the development and execution of overall clinical supply strategy and management for clinical development program(s), including management of investigational medicinal product (IMP) for assigned global trials
- Oversees and supports clinical study planners in a matrix environment; facilitates issue and risk identification, mitigation, resolution and communication
- Drives decision-making at cross-functional teams (ClinOps, PDM sub-teams) supporting the long-term vision
- Identifies, manages and mitigates supply risks at clinical development program level
- Leads and drives visible, impactful process improvements, change business and organizational imperatives
- Authors, revises and reviews standard operating procedures (SOPs), work instructions and business policies
- Accountable for clinical supply budget of assigned clinical development program(s)
- Reviews and approves statement of work, purchase orders and invoices
- Influences, at times drives, program allocations at partners, contract manufacturing organizations (CMOs)
- Leads or contributes to GCSC, GSC or PDM strategic initiatives including due diligence resource pool, global drug delivery community, clinical supply integration due to M&A and policy topic member supporting the External Advocacy Steering Team (EAST)
Skills
Supply Chain Planning
Clinical Supply Chain
Inventory Management
Manufacturing Planning
Distribution Management
Protocol Design
Regulatory Compliance
Project Management
Quality Assurance
Global Supply Chain
Gilead Sciences
Develops and commercializes biopharmaceuticals
About Gilead Sciences
Gilead Sciences focuses on discovering, developing, and commercializing medicines for various medical conditions, including HIV/AIDS, liver diseases, cancer, inflammatory and respiratory diseases, and cardiovascular issues. The company conducts extensive research and development to create new therapies, which are then marketed to healthcare providers, hospitals, and pharmacies after receiving regulatory approval. Gilead differentiates itself from competitors through its strong commitment to R&D and strategic partnerships, such as with SAP Ariba, to enhance its operations and product offerings. The company's goal is to improve health equity and access to care globally, working with communities to ensure that its medicines reach those in need.
Foster City, CaliforniaHeadquarters
1987Year Founded
$15,873.6MTotal Funding
IPOCompany Stage
Biotechnology, HealthcareIndustries
10,001+Employees