Quality Control Analyst Ii

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 Seagen Quality Control (QC) Canyon Park Testing team is dedicated to supporting the release and stability testing of both our commercial and clinical stage programs. This position is responsible for performing the routine and non-routine testing with proficiency and general QC laboratory work for the in-process support, release and/or stability of Seagen’s clinical development and/or commercial products in a GMP testing environment.
Principal Responsibilities:

• Supporting special projects for potency/analytical problem solving
• Troubleshooting laboratory or system anomalies (with guidance)
• Fully comply with company health and safety procedures and practices
• Creating and revising standard operating procedures (SOP’s) and other documents as needed
• Identifying and participating in continuous improvement projects
• Maintain training to current standards and procedures on all assigned curriculums
• Performing maintenance of QC lab equipment, procedures and systems
• Applying the principles of good manufacturing practices (GMP) daily
• Performing sample testing for stability or release testing

Required Qualifications:

• Proficient with Microsoft Applications (Word, Excel, Outlook, SharePoint, etc.)
• Some experience with troubleshooting and/or an understanding of the listed equipment.
• Be highly organized with an attention to detail
• Associate degree in a relevant field with 2 years of experience or a bachelor's degree in a relevant field (in addition to 2+ years of relevant experience)
• 2+ years of experience working in a GMP regulated environment (GMP, GLP etc.).
• Strong technical writing and communication skills
• Strong data interpretation/analytical skills

Preferred Qualifications:

• Experience with a LIMS or other sample/inventory management system
• Experience with Analytical Software i.e. Empower, 32 Karat
• Experience authoring or revising Standard Operating Procedures

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 $70,000 to $90,000 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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