Seagen
Quality Control Analyst I/II
Technical Operations & Process Sciences - Bothell, United States
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
Performs lab support activities and participates 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
- Performing sample testing primarily using basic test methods (pH, osmolality, particulate matter, etc) while training on more advanced plate-based methods
- Performing maintenance of QC lab equipment, procedures and systems
- 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
- Fully comply with company health and safety procedures and practices
Additional responsibilities for QC Analyst II:
- Reviewing sample testing
- Performing sample testing primarily using plate-based potency methods
- Creating SOP’s and other documents as needed
Required Qualifications:
- Associates degree with 2+ years of experience in a relevant field 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
Additional Qualifications for QC Analyst II:
- Experience with basic lab equipment (pH meters, balances, pipettes, etc.)
Experience with cell culture and plate-based assays
- Proficient in sterile technique
Preferred Qualifications:
- 0-2 years of experience working in a GMP laboratory
Additional Qualifications for QC Analyst II:
- 2+ years of experience working in a GMP Laboratory
- Experience authoring or revising SOPs
- Experience with LIMS or other sample/inventory management system
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.
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: 07/29/2022
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