Seagen

Supervisor Cell Culture Manufacturing - Launchpad

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:

Seagen is seeking a highly motivated Supervisor, Cell Culture 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).

Principal Responsibilities:

• Supervise the execution of all upstream operations, including systematic pre-production walk down/checks, assemblies/cleaning/sterilization of equipment, preparation of solutions and media, cell culture and recover operations
• Taking active role in developing less experienced staff; providing coaching and mentoring; managing personnel performance review
• Creates and revises SOPs (standard operating procedures) and MBRs (master batch records) as appropriate
• Developing and maintaining operations schedule in conjunction with area manager and planning team
• Managing daily coordination of workload among team members; provides shift handover working directly with other supervisors; primary point-of-contact for the upstream area over assigned shift
• Developing and demonstrating proficiency in Quality Systems, including investigations, change control, and corrective/preventative actions
• Authoring/reviewing/improving manufacturing documents, technical reports, training documentation and validation documents as needed
• Developing and demonstrating proficiency in process automation and business quality systems and software
• Participate and support a culture of continual improvement. Effectively collaborate with cross functional partners such as Quality Assurance, Quality Control, Supply Chain, and Facilities

Required Qualifications:

• Bachelor’s degree preferably in Life Sciences or Engineering, or associate degree preferably in Life Sciences or a technical program, or High School
• Diploma with Biotech certificate from an approved program desirable
• A minimum of 6+ years of experience operating in a cGMP biopharmaceutics manufacturing facility is desired 1-2+ years of leadership experience desired
• Must be able to work weekends, off-shifts, and overtime as required. Applicant must be willing and able to work reliably on a flexible schedule, Monday – Friday and some weekends, to meet the demands of the project
• Demonstrated ability to lead manufacturing operations teams to achieve objectives; previous supervisory experience is desired
• Adaptable to a fast-paced dynamic business environment
• Experienced in large-scale cell culture and recovery operations experience is essential; fermentation experience is a plus
• Good organizational and communication skills, both written and verbal, and the ability to prioritize competing tasks
• Engages in and supports a culture of continual improvement; is attentive and approachable
• Demonstrated knowledge of cGMP regulations
• Effective communication skills and ability to work well on teams and cooperate across organization to solve problems
• Experience in preparing data for reports and presentations and some experience in technical report writing
• Excellent interpersonal skills with the ability to work well with others in a dynamic and highly collaborative environment

Preferred Qualifications:

• BA/BS degree in a scientific discipline (life sciences / engineering)
• Previous leadership experience desired
• Hands on experience with disposable/single use technology (i.e., single-use bioreactors, single-use mixing and storage systems)

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.

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Seagen

Seagen is an Equal Opportunity Employer

Submitted: 01/27/2023