Job Description

Description

Position at Seagen

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 routine and non-routine testing with expert proficiency and general QC laboratory work for release of Direct Raw Materials to support 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 maintenance of QC lab equipment, procedures and systems 

  • 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 

  • Fully comply with company health and safety procedures and practices 

  • Preparing buffers used for QC Testing 

  • May require lifting/moving heavy objects

  • Performing sample testing for raw material release testing 

  • Weekend, Holiday, overtime, and off-hour work may be required as needed to support manufacturing

    • Expected Qualifications: 

  • Associates degree 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 

    • Preferred Qualifications: 

  • 0-2 years of experience working in a GMP laboratory 

    •  The hiring pay range for this position is $56,000 - $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 and an annual bonus. 

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