Associate Director Pharmaceutical Sciences

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 Associate Director is a skilled professional who leverages scientific expertise to provide leadership within Pharmaceutical Sciences. The Associate Director’s expertise enables them to be a forward thinking and skilled business partner with senior leaders in the organization. The role is a blend of tactical and strategic work. The Associate Director contributes to formulating the strategy and long-term vision of their function. 

The Associate Director will lead a group, supervising direct reports or cross-functional teams (internal or external). The Associate Director has decision making authority focused on their own functional area with consideration of impacts to relevant stakeholders. Decision-making is with the support and buy-in of their management. 

Principal Responsibilities: 

• Builds external collaborations to advance industry best practices in drug development and manufacturing
• Provides technical, managerial, and strategic leadership within Pharmaceutical Sciences
• Oversees and mentors representatives on early, late, and commercial CMC teams, technology innovation, and cross-functional initiatives
• Oversees relevant CMC sections of regulatory submissions and may serve as a subject matter expert in regulatory interactions
• Encourages and facilitates career development of staff. Fosters effective teamwork and communication amongst staff. Builds a reputation for excellence both as an individual and as a team
• Supports development and/or manufacturing activities at both internal and external manufacturing organizations
• Cultivates excellent working relationships with key stakeholders to deliver successful project outcomes
• May contribute to resource and budget planning for functional area
• Manage a group of scientists and research associates within the department of Pharmaceutical Sciences. Integrate activities of this group to develop stable formulation and robust DP manufacturing processes
• Collaborates effectively with cross-functionally with non-Clinical, Clinical, and Commercial, to meet timeline and product development requirements

Required Qualifications: 

• Degree in Pharmaceutical Sciences, Biochemistry, Biological Sciences, Chemical Engineering, or related discipline
• B.S. and 20+ years; M.S. and 17+ years; Ph.D. and 8+ years experience
• Demonstrated expertise in biologics development within the pharmaceutical industry
• Strong interpersonal skills/communication skills and experience with cross-functional mentorship and influence to enable execution of complex global projects
• Previously provided support establishing department/functional area strategy and demonstrated people management skills
• At least half of industry experience performing protein formulation development, analytical and biophysical characterization or DP process development including lyophilization processes development, technology transfer to CMOs, DP CMO management
• Familiarity with quality guidelines for pharmaceutical industry and regulatory submissions in US and Europe
• Excellent organizational and communication skills
• Proven record of supervising, mentoring, and developing staff
• Demonstrated ability to collaborate and lead cross-functional technical teams

Preferred Qualifications: 

• Subject matter expertise in drug product process development of lyophilized and/or liquid biologic products
• Proven experience of developing DP in multiple presentations, for example vial, pre-filled syringe, auto-injectors etc.

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 $174,000 to $226,000 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 (with additional annual grants, and grants upon promotion when applicable), 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. 

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