Quality Control Analyst II

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 the in-process support, release and / or stability of Seagen’s clinical development and / or commercial products in a GMP testing environment.

Must be able to work weekends, off-shifts, and overtime as required. Holiday work may be 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.

Principal Responsibilities :

Applying the principles of good manufacturing practices (GMP) on a daily basis

Performing sample testing for in-process, release, or stability testing

Performing maintenance of QC lab equipment, procedures, and systems

Creating and revising standard operating procedures (SOPs) and other documents as needed for change or improvement

Identifying and leading continuous improvement projects

Maintain training to current standards and procedures on all assigned curriculums

Fully comply with company health and safety procedures and practices

Participate in the qualification and validation of test methods

Troubleshoot laboratory or system anomalies (with guidance)

Required Qualifications :

Associate’s 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)

Broad experience with Microsoft Office products

Highly organized with an attention to detail

Experienced in various analytical lab equipment (balances, CE / iCIEF, HPLC / UPLC, osmometers, pH meters, pipettes, plate readers, SoloVPE,

Preferred Qualifications :

2+ years of experience working in a GMP laboratory

The hiring pay range for this position is $70,000 - $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 and an annual bonus.