Seagen

Senior Manager Global Planning

Technical Operations & Process Sciences - Remote, Bothell, United States

Description

Seagen is a global, multi-product biotechnology company dedicated to developing and commercializing transformative cancer medicines. As the industry leader in antibody-drug conjugate (ADC) technology, we pioneered a new generation in the science of harnessing antibodies to deliver cell-killing agents directly to cancer cells. Seagen’s dedication to improving the lives of cancer patients goes beyond science, and we believe that every employee has a role in contributing to this mission. By working together with a shared dedication and diverse perspectives, we are able to reach our full potential and make a real difference in the world. Seagen is a fast-growing company and has an abundance of opportunities available for you to grow your career. Put your passion to work at Seagen and join us!

Summary

The Global Supply Chain Senior Manager is a member of a team charged with ownership of end to end alignment of Demand and Supply planning for Seagen Commercial, Partner, and Clinical Products. This position will be key in managing, analyzing, reporting, and executing the Integrated Business Planning process working with cross functional stakeholders in Finance, Commercial, Operations, and Regulatory.

Principal Responsibilities:

• Participates as the key Supply Chain owner for the assigned product by providing strategic insights on the Supply Product Team.
• Own the Supply Operations Sub team to direct and align the various Supply Operations functions for the product.
• Manage and document Product Demand and Supply assumptions.
• Collect and summarize product requirements from Commercial, Partner, Operations, and Clinical sources.
• Supply Plan Consensus demands into safety stock and dependent demand requirements for downstream materials.
• Monitor production with multiple contract manufacturers across the stages.
• Continuously develops, analyzes, and maintains long-range supply plan.
• Responsible for balancing demand requirements with the Manufacturing network operational capacity and contractual requirements.
• Participates and provides input into commercial supply agreements.
• Monitor work-in-process activities for supply chain batch release to ensure on-time delivery and/or address impact of delays providing direction for prioritization of changes.
• Determines material supply allocation to support clinical and commercial country market needs.
• Monitor supply adherence of site execution of detailed planning requirements.
• Monitors demand against forecast and adjusts supply plans as required.
• Monitors regulatory submissions and approval dates to ensure appropriate supply is designated for approved regions.
• Embraces the use of standard demand and supply planning tools and serve as a power user.
• Supports IBP process for products and provide detailed review of inventory and planned manufacturing through supply chain.
• Conduct scenario analyses to support optimal supply strategies as required.
• Basic understanding of accounting principles for business/finance analyst interactions.
• Supports SOX audits and finance team as subject expert in Production Planning and Inventory Management.

Qualifications:

• Minimum of 7 years of multi-disciplinary experience in the pharmaceutical/biotech industry, preferably with experience in global cross-functional drug development.
• Late-stage program/project management, regulatory submission planning and/or commercial launch experience highly desirable.
• Drug Development knowledge with understanding of other functions relevant to the position which may include: Research, Preclinical, Clinical, Manufacturing, Regulatory and Commercial.
• Excellent business acumen, demonstrated ability to align teams to strategy to achieve business and project objectives.
• Experience leading and facilitating project team meetings, cross-functional communication and decision making, and ensuring ongoing alignment with internal/external stakeholders.
• A proactive and/ strategic thinker, with strong facilitation, problem-solving and issue resolution skills.
• Highly collaborative with outstanding communication and relationship management skills, high emotional intelligence.
• Adaptive leadership style with ability to influence teams without formal authority.
• Ability to work effectively with cross-functional teams in a highly matrixed global organization.
• PMP credential and experience with latest PM tools, software and processes highly valued.
• Experience in biologics and oncology, experience working with corporate partners and alliances is desirable.

Education:

• Bachelor’s Degree required. Advanced degree (MS, MBA, Ph.D.) in biomedical sciences, business or other disciplines related to drug development highly preferred.

As the leading employer in our industry in the Pacific Northwest, Seagen is proud to offer a competitive total compensation package as well as a comprehensive benefits program designed to support the whole lives of our employees and their families. Benefits include medical, vision and dental coverage, group and supplemental life insurance, 401(k) with company match, tuition reimbursement, relocation assistance and much more. To learn more about Seagen, visit www.seagen.com.

Seagen is an equal opportunity employer. All qualified applications will receive consideration for employment without regard to race, age, gender identity, sexual orientation, color, religion, sex, marital status, national origin, protected veteran status, disability status, or any other status protected by federal, state, or local law.

To prevent the spread of COVID-19, and as an integral part of its public health and safety measures, Seagen requires that all newly-hired employees be fully vaccinated against COVID-19 before commencing employment, subject to reasonable accommodation and other requirements of applicable federal, state, and local law.

Apply:

Seagen

Seagen is an Equal Opportunity Employer

Submitted: 05/20/2022