Seagen

Director Site Supply Operation

Technical Operations & Process Sciences - 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!

Position Summary:

The Director of Site Supply Operations is a key member of Seagen North Creek Site Leadership Team and is accountable for master production scheduling, materials management (planning, procurement, purchasing), warehouse operations, and site project management.

The candidate will lead a team of 12+ Supply Chain professionals to achieve North Creek site goals in close partnership with Manufacturing, Quality Control, Quality Assurance, MSAT, Process Engineering, EHSS, Global Supply Chain, and Finance. The candidate is expected to have extensive knowledge across functional areas and resources related to manufacturing of biologics and supply chain management. The candidate will own the operational performance associated with production planning, raw materials supply and inventory, and warehouse operations.

Principal Responsibilities:

• Directs warehouse activities (including shipping, receiving, intra and inter-site transfers, and storage) and works directly with Materials planners to ensure that manufacturing Bill of Materials are accurate to support proper procurement of raw materials needed for clinical and commercial mAb manufacturing
• Directs site scheduling and issuance teams which includes the responsibility for providing the manufacturing schedule to all operations units
• Directs site planning analysts in the development of the site master plan, site production risks and mitigation strategies and lead and develop site S&OP
• Leads, coaches, develops a team of site Supply Chain, Materials Management, Production Schedulers and Project Manager staff. Grows team as directed by business scope
• Acts as Global Supply Operations point of contact across Manufacturing sites, develops strong business relationships, and advocates for North Creek interests
• Leads timely and comprehensive communication of forecast, purchase orders, quantity, and lead-time requirements to appropriate internal and external stakeholders (GMP material suppliers, logistics service providers)
• Co-leads product lifecycle by translating strategy into site supply chain plans and oversees successful execution
• Develops and executes annual budget as guided by site and corporate plans Co-leads supply chain systems and process implementation
• Works closely with internal and external resources to optimize supply availability and inventory investment
• Oversees warehouse operations at the North Creek facility and the satellite B15 warehouse and collaborates with other internal manufacturing facilities
• Drives continuous improvement projects to increase efficiency, maturity, and compliance for all areas of responsibility
• Assists in technical problem solving and partners with Manufacturing, Quality, and other stakeholders to resolve technical and compliance issues
• Leads and execute high-profile Supply Operations projects
• Acts as Site Supply Chain representative for recall planning process/team

Qualifications:

• A minimum of 10+ years working in a global biopharmaceutical Supply Chain or related industry
• A minimum of 5-8 years working within a pharmaceutical environment
• In-depth functional knowledge of site supply chain, warehouse operations, master production scheduling, raw materials planning, procurement, and purchasing
• Working experience in commercial supply product launches
• Demonstrated knowledge of global manufacturing regulations and best practices
• Experience and knowledge of cGMPs in an FDA regulated environment
• Experience working within an integrated enterprise level planning system (Oracle preferred)

Education:

• PhD with 6-8 years of experience
• MS or MBA with 8-12 years of experience
• Bachelors with 12+ years of experience is desired

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, please visit www.seagen.com.

The hiring pay range for this position is $186,000 to $241,000 per year based on skills, education and experience relevant to the role. Other components of total compensation include a competitive equity grant at the time of hire and an annual bonus.

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.

Apply:

Seagen

Seagen is an Equal Opportunity Employer

Submitted: 11/17/2023