BeiGene, Ltd.

Manager/Senior Manager, Clinical Supply Chain

BeiGene, Ltd. • $114K — $154K *
US-AnywhereRemote in United States
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor’s or Master’s degree in Business Administration, Operations Management, or related field.
  • Minimum of 5 years of progressive supply chain experience, preferably in biotech, pharmaceutical, or CRO settings.

Responsibilities

  • Represent Clinical Supply Chain in clinical study teams, providing high service to internal stakeholders.
  • Collaborate with Clinical Operations to align supply plans with clinical demand.
  • Create and manage inventory and production schedules for clinical trial materials.
  • Monitor production schedule adherence and initiate necessary course corrections.
  • Oversee GMP inventory management and ensure drug accountability.
  • Manage daily activities with CMOs and distribution vendors as well as internal teams.
  • Investigate exceptions to supply plans, implementing corrective actions and closures.

Benefits

  • Comprehensive medical, dental, and vision insurance.
  • 401(k) retirement plan with company matching.
  • Flexible Spending Account (FSA) and Health Savings Account (HSA) options.
  • Life insurance coverage and wellness programs.
  • Paid time off to support work-life balance.
  • Employee stock options and participation in a stock purchase plan.
Full Job Description

General Description:

  • The Manager of Clinical Supply Chain manages drug supply activities related to planning, label development, label & pack, and distribution for one or more clinical programs. Actively develops and oversees supply plans to ensure accurate and continuous supply to patients while reducing risk and minimizing waste. Represents Clinical Supply Chain to internal stakeholders and manages relationships with external supply partners. Has a working knowledge of clinical supply best practices, IRT systems, as well as experience working within a cGMP environment. Works with management to develop and implement process improvements to build the organization for the future.

Essential Functions:

  • Represent the Clinical Supply Chain on Clinical Study Teams (CST) and provide a high service level to internal stakeholders (e.g. Clinical Operations, Regulatory, Quality, CMC).
  • Work with Clinical Operations to understand clinical demand requirements and ensure alignment with study teams to supply plans and timelines.
  • Create supply and inventory plans and develop production schedules for clinical trial materials.
  • Monitor schedule adherence of production schedules and make course corrections if needed.
  • Manage GMP inventory throughout the supply chain, develop inventory reports, manage upcoming expiry, and ensure drug accountability.
  • Oversee daily activities for FG label & pack CMOs and distribution vendors with internal stakeholders.
  • Responsible for investigation of exceptions to determine root causes, implement CAPAs and drive closure.
  • Ensure label text and proofs are in accordance with applicable rules, regulations, product specifications, and clinical study protocol(s).
  • May coordinate review and approval of labels with stakeholders (e.g. Regulatory, Clinical Operations, CRO) and CMOs.
  • Support IRT user acceptance testing, develop IRT supply strategy (DNX parameters), and oversee ongoing supply activities in system.
  • Coordinate and track bulk shipments to CMOs, depots, and vendors. Maintain and track import licenses.
  • Develop supply strategies to maximize supply efficiency, minimize waste while identifying risk and develop risk mitigation plans
  • Supports functional projects and process improvements related to drug supply. Assist in the creation or revision of process documents such as Standard Operating Procedures.
  • Ensure staff who are in supportive roles for supply planning and business process development are meeting deliverables for successful study management.

Education/Experience Required:

  • Bachelor’s or master’s degree in business administration, Operations Management, or a related field required.
  • Minimum of 5 years of progressive experience in supply chain, preferably within the biotech, pharmaceutical, or CRO industry.

Global Competencies

When we exhibit our values of Patients First, Driving Excellence, Bold Ingenuity and Collaborative Spirit, through our twelve global competencies below, we help get more affordable medicines to more patients around the world.

  • Fosters Teamwork
  • Provides and Solicits Honest and Actionable Feedback
  • Self-Awareness
  • Acts Inclusively
  • Demonstrates Initiative
  • Entrepreneurial Mindset
  • Continuous Learning
  • Embraces Change
  • Results-Oriented
  • Analytical Thinking/Data Analysis
  • Financial Excellence
  • Communicates with Clarity

Salary Range: $114,600.00 - $154,600.00 annually

BeOne is committed to fair and equitable compensation practices. Actual compensation packages are determined by several factors that are unique to each candidate, including but not limited to job-related skills, depth of experience, certifications, relevant education or training, and specific work location. Packages may vary by location due to differences in the cost of labor. The recruiter can share more about the specific salary range for a preferred location during the hiring process.  Please note that the listed range reflects the base salary or hourly range only. Non-Commercial roles are eligible to participate in the annual bonus plan, and Commercial roles are eligible to participate in an incentive compensation plan. All Company employees have the opportunity to own shares of BeOne Medicines Ltd. stock because all employees are eligible for discretionary equity awards and to voluntarily participate in the Employee Stock Purchase Plan. The Company has a comprehensive benefits package that includes Medical, Dental, Vision, 401(k), FSA/HSA, Life Insurance, Paid Time Off, and Wellness.

About BeiGene, Ltd.

BeiGene, Ltd. is a biotechnology company that develops and commercializes innovative cancer treatments. The company was founded in 2010 and is headquartered in George Town, Grand Cayman. BeiGene's portfolio includes several drug candidates that target cancer cells and the tumor microenvironment. The company's lead product, Brukinsa, is a treatment for mantle cell lymphoma that has been approved by the U.S. Food and Drug Administration (FDA) and the European Medicines Agency (EMA). BeiGene also has partnerships with several pharmaceutical companies, including Amgen, Merck, and Novartis.
Learn more about BeiGene, Ltd.
Size
8,300 employees
Market Cap
$22.2 billion
Industry
Net Income
-$1.5 billion
Founded
2010
5 Year Trend
+305.7%
Revenue
$308.8 million
NASDAQ

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