Celgene QC Associate III in Bothell, Washington
Celgene is a global biopharmaceutical company committed to changing the course of human health through bold pursuits in science, life-enhancing therapies, and a promise to always put patients first. At the core of that mission are the talented individuals who contribute their unique skill sets to help us drive innovation and deliver truly life-changing drugs for our patients. As we continue to pursue that mission, we’re looking for talented professionals like you to join our team. What unique gene will you bring to Celgene?
This is a Sun - Wed PM Shift (1:30pm - Midnight)
The primary focus of the QC Associate II / III role will be to perform GMP testing to support product lot release and in-process testing.
Good Manufacturing Practices (GMP) testing to support QC product release and in-process testing
Support assay transfer and method validation by executing ross-site validation protocols, and providing data to support final reports
Assist in the implementation of new assay methodologies and the associated instrumentation
Act as a lead in small scale projects
Performance of instrument preventative maintenance with complete and concise supporting documentation in a GMP compliant manner
Participation in cross-functional assay training
3+ years experience in Flow Cytometry is preferred
Ability to work in a high paced team environment, meet deadlines, and prioritize work from multiple projects
Detail-oriented with strong time-management skills
Excellent communication skills, with the ability to work effectively with others
Ability to adjust to a dynamic work environment
Experience working in a regulated (GxP) environment
Computer proficiency with Office
BS in a scientific discipline with 6+ years of regulated industrial analytical testing or QC experience, or equivalent combination of education and experience.
At Celgene, we seek to deliver truly innovative and life-changing drugs for our patients. Our mission is to focus on the discovery, development, and commercialization of products for the treatment of cancer and other severe, immune, inflammatory conditions. Energizing this mission are the uniquely talented individuals that bring their passion, creativity, and innovation to work every day. Bring your unique gene to our team.
Celgene is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Celgene complies with all applicable national, state and local laws governing nondiscrimination in employment as well as employment eligibility verification requirements of the Immigration and Nationality Act. All applicants must have authorization to work for Celgene in the U.S.COMMITTED TO IMPROVING THE LIVES OF PATIENTS WORLDWIDE