Director, Comparator Sourcing, Clinical Supply - Emeryville, United States - BeiGene

    BeiGene
    BeiGene Emeryville, United States

    3 weeks ago

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    Description

    The Director of Comparator Purchasing, Clinical Supply Chain is responsible for overseeing the Clinical Supply Chain vision and strategy providing leadership over the comparator purchase strategy and timely delivery management. Ensures organization effectively manages relationships with procurement and vendors as needed and acts as point of escalation for the planning organization on issues for comparator provision. The position provides leadership, manages direct reports as well as mentors team members as required to ensure optimal performance. Represents the function on the Global Clinical Supply Chain Leadership Team and ensures strategic alignment to Global Clinical Supply Chain and BeiGene's strategic goals. Builds strong relationships with BeiGene functional leadership (including but not limited to global clinical supply planning and GRDS) to ensure alignment of organizations and prompt resolution of critical issues.

    Has an expert working knowledge of supply chain best practices and experience working within a cGMP and GCP environment. Has strong cross-cultural awareness and communication skills to lead in a fast paced, multi- cultural company.

    Essential Functions:

    • Oversees the collaboration with the Clinical Supply Chain Planning organization to understand the comparator requirements for clinical studies.
    • Partners with the global procurement management to build a strategy for comparator sourcing in support of the organization's portfolio.
    • Establishes an infrastructure for collection of comparator information, ensuring internal expertise is established for types of comparators on market, including pack sizing.
    • Ensures on time responses between the Clinical Supply Chain Planning organization and procurement teams in support of delivery for the required comparators on time.
    • Ensures support is provided to the Clinical Supply Chain Planning organization in providing supporting documentations from vendors.
    • Ensures tracking of target delivery to CMOs supporting release activities.
    • Responsible for investigation of exceptions to determine root causes, implement CAPAs and drive closure.
    • Develops sourcing strategies to maximize supply efficiency, minimize waste while identifying risk and develop risk mitigation plans
    • Builds a team to support the comparator purchase strategy for the department.
    • Builds strategic relationships with internal functional groups and ensures alignment.
    • Participates and lead process/performance improvement initiatives with cross functionally with stakeholders contributing to global/regional initiatives or programs.
    • Participates in monthly Supply Review Meeting of CD&OP and present/report comparator supply delivery performance and related discussions as required.
    • Ensures robust systems and processes are in place to enable execution of operational and logistical tasks in a cGMP compliant manner.
    • Collaborates and author department policies and procedures.
    • Leads staff who are in supportive roles for supply planning and business process development

    Supervisory Responsibilities:

    Lead comparator sourcing team for BeiGene. Manage direct reports as well as provide mentoring to their teams as required.

    Competencies:

    • Experience working in a global, complex supply chain organization within the biopharma industry.
    • Experience leading multi-disciplinary department(s) and building up the team
    • Strong ability to collaborate and build strategic relationships with internal (Clinical Operations, Quality,

    CMC, Regulatory, etc.) stakeholders.

    • Demonstrates advanced knowledge of global clinical trials and the drug development process.
    • Experience in vendor oversight and managing external partnerships and relations.
    • Experience with comparator sourcing
    • Understanding of IRT system functionality and Excel modeling.
    • Understands comprehensive global pharmaceutical regulatory requirements (e.g. cGMP, ICH/GDP, GCP, 21 CFR Part 11, and Annex 13).
    • Experience in deviation investigation and CAPA implementation.
    • Ability to work effectively in cross-functional and multi-cultural teams.

    Education Required:

    Bachelor or Master Degree in Business Administration, Operations Management, or similar education required.

    12+ years progressive experience in Supply Chain preferably within the biotech, pharmaceutical, CRO, industry with 5+ years in comparator sourcing

    5+ years of people leadership and development experience

    Ethics - Treats people with respect; Inspires the trust of others; Works with integrity and ethically; Upholds organizational values.

    Planning/Organizing - Prioritizes and plans work activities; Uses time efficiently. Completes administrative tasks correctly and on time. Follows instructions and responds to management direction.

    Communication - Listens and gets clarification; Responds well to questions; Speaks clearly and persuasively in positive or negative situations. Writes clearly and informatively. Able to read and interpret written information.

    Teamwork - Balances team and individual responsibilities; Gives and welcomes feedback; Contributes to building a positive team spirit; Puts success of team above own interests; Supports everyone's efforts to succeed. Contributes to building a positive team spirit; Shares expertise with others.

    Adaptability - Able to adapt to changes in the work environment. Manages competing demands. Changes approach or method to best fit the situation. Able to deal with frequent change, delays, or unexpected events.

    Technical Skills - Assesses own strengths and development areas; Pursues training and opportunities for growth; Strives to continuously build knowledge and skills; Shares expertise with others.

    Dependability - Follows instructions, responds to management direction; Takes responsibility for own actions; Keeps commitments; Commits to long hours of work when necessary to reach goals; Completes tasks on time or notifies appropriate person with an alternate plan.

    Quality - Demonstrates accuracy and thoroughness; Looks for ways to improve and promote quality; Applies feedback to improve performance; Monitors own work to ensure quality.

    Analytical - Synthesizes complex or diverse information; Collects and researches data; Uses intuition and experience to complement data.

    Problem Solving - Identifies and resolves problems in a timely manner; Gathers and analyzes information skillfully.

    Project Management - Communicates changes and progress; Completes projects on time and budget.

    Computer Skills : Efficient in Microsoft Word, Excel, and Outlook

    Other Qualifications :

    Travel:

    All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.