Seagen

Supervisor, Purification Drug Substance Manufacturing - Launchpad

Technical Operations & Process Sciences - Bothell, United States

Description

Summary:

Seagen is seeking a highly motivated Manufacturing Supervisor, Purification Drug Substance, that desires an opportunity to significantly contribute to the development and commercialization of transformative cancer therapies. The initial focus of this position will be to actively participate and contribute to the design, build, and operational startup of Seagen’s new cGMP manufacturing facility, “Project Launch Pad” being built in Everett, Washington, just North of Seattle. Launch Pad will be a greenfield build encompassing end-to-end manufacturing capabilities for biologics and antibody-drug conjugates (ADCs).

Requirements or Responsibilities:

• Performs oversight of purification operations, including assembly/cleaning/sterilization of equipment, preparation of solutions, and systemic pre-production walk down/checks, ensuring they are executed safely and in accordance with cGMP guidelines.
• Authors/reviews/improves manufacturing documents, technical reports and validation documents as needed.
• Coaches/mentors less experienced manufacturing associates and actively involved in managing personnel performance review.
• Manages daily coordination of workload among team members and shift handover working directly with other supervisors; primary point of contact for the downstream area during assigned shift. Ensures purification team maintains a clean and orderly production area.
• Positively engages and collaborates with other team members to ensure daily production tasks are completed promptly.
• Leads or assists with scheduling and execution of production tasks including campaign startup and product changeover. Coordinates communication with cross functional partners and management regarding production updates and delays in schedule.
• Demonstrates proficiency in Quality Systems, including deviation investigations, change controls, and corrective/preventative actions.
• Escalates any production issues or abnormalities to management and other cross functional groups. Provides insight and recommendations to address production issues and oversees the execution of any non-routine or troubleshooting activities.
• Participates and supports a culture of continuous improvement. Effectively collaborates with cross-functional partners like Quality Assurance, Quality Control, Supply Chain, and Facilities.

Qualifications:

• Bachelor’s degree preferably in Life Sciences or Engineering, or Associate degree preferably in Life S
• 6+ years of cGMP experience
• Ability to follow detailed instructions and maintain accurate records and notes
• Knowledge of purification mAb production operations and equipment
• Demonstrated ability to lead manufacturing operations teams and work effectively in a team environment
• Exceptional skills working cross functionally with individuals across multiple functional groups
• Excellent oral and written communication skills
• Ability to work occasional weekends, holidays or overtime as needed
• Skills in problem solving and troubleshooting
• Demonstrated organizational and leadership skills regarding project management
• Excellent technical writing skills
• Ability to lift up to 20 Kg
• Familiarity with MS Office applications (Word, Excel)

Preferred Qualifications:

• BA/BS degree in a scientific discipline (life sciences / engineering)
• Previous supervisory experience desired
• Previous experience with single use technology in the biopharmaceutical industry

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 $99,000 - $127,600 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.

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: 01/27/2023