You haven't searched anything yet.
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 QA Associate II is responsible for performing day to day activities related to Quality Document Control (QDC) and GMP Records filing systems for both physical and electronic records. QDC will own and manage the GMP Quality business processes supporting Quality Document Control authoring, review, approval, and archive of GMP lifecycle documents,
The QDC responsibilities include following the corporate requirements for the Document Control program, making decisions within the scope of the program, while providing strong customer service and user support by answering questions and providing guidance.
Principal Responsibilities:
Expected Qualifications:
Preferred Qualifications:
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 $71,000 - $92,000 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.
#LI-KC1
Full Time
Durable Manufacturing
$77k-95k (estimate)
02/10/2023
05/03/2024
seattlegenetics.com
BOTHELL, WA
1,000 - 3,000
1997
CLAY B SIEGALL
$1B - $3B
Durable Manufacturing
The job skills required for Quality Assurance Associate II include Customer Service, Problem Solving, Continuous Improvement, etc. Having related job skills and expertise will give you an advantage when applying to be a Quality Assurance Associate II. That makes you unique and can impact how much salary you can get paid. Below are job openings related to skills required by Quality Assurance Associate II. Select any job title you are interested in and start to search job requirements.
The following is the career advancement route for Quality Assurance Associate II positions, which can be used as a reference in future career path planning. As a Quality Assurance Associate II, it can be promoted into senior positions as a Quality Assurance Specialist III that are expected to handle more key tasks, people in this role will get a higher salary paid than an ordinary Quality Assurance Associate II. You can explore the career advancement for a Quality Assurance Associate II below and select your interested title to get hiring information.