Seagen
Quality Control Analyst I
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:
Performs support activities to ensure continuity of supply of critical reagents for plate-based methods to support QC laboratories across internal and external sites. May provide support and participate in basic routine and non-routine testing 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:
- Applying the principles of good manufacturing practices (GMP) on a daily basis
- Creating and revising standard operating procedures (SOPs) and other documents as needed
- Identifying and leading continuous improvement projects
- Maintain training to current standards and procedures on all assigned curriculums
- Preparing buffers used for QC Testing
- Performing basic critical reagent qualification testing for plate-based methods
- Coordinating shipment of critical reagents
- Supporting inventory verification of critical reagents in QC to support routine testing
- Fully comply with company health and safety procedures and practices
Expected Qualifications:
- Associate’s degree in a relevant field with 2 years of experience or a Bachelor's degree in a relevant field
- Broad experience with Microsoft Office products
- Highly organized with an attention to detail
- Knowledge of biological and/or chemical handling
- Able to handle multiple tasks in an organized and time-efficient manner
- Strong technical writing and communication skills
Preferred Qualifications:
- 0-2 years of experience working in a GMP Laboratory
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 $56,000 to $73,000 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.
Apply:
Seagen
Seagen is an Equal Opportunity Employer
Submitted: 09/08/2023
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