Seagen

Supervisor Upstream Manufacturing

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!

Summary:

The North Creek Manufacturing Facility at Seagen is seeking a Supervisor, Upstream Manufacturing. The supervisor uses their knowledge and experience of upstream biopharmaceutical processing to perform and oversee manufacturing operations in a cGMP facility. This position reports to the Manager of Upstream Manufacturing.

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 experience staff; providing coaching and mentoring; managing personnel performance review
• 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, 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’s degree preferably in Life Sciences or a technical program, or High School Diploma with Biotech certificate from an approved program desirable
• A minimum of 8+ years of experience operating in a cGMP biopharmaceutics manufacturing facility is 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
• Must be able to don gowning in the form of hospital scrub, gloves, safety glasses/goggles, coveralls and safety toe footwear with shoe covers multiple times per shift
• Handle and work with hazardous materials and chemical per standard operating procedures and OSHA guidelines
• 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
• Hands on experience with disposable/single use technology is essential (i.e., single-use bioreactors, single-use mixing and storage systems)
• 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)

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.

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.

The hiring pay range for this position is $99,000 to $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.

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: 12/09/2022