Celgene is a global biopharmaceutical company leading the way in medical innovation to help patients live longer, better lives. Our purpose as a company is to discover and develop therapies that will change the course of human health. We value our passion for patients, quest for innovation, spirit of independence and love of challenge. With a presence in more than 70 countries, and growing - we look for talented people to grow our business, advance our science and contribute to our unique culture.
This Associate Manager is responsible for the continuous improvement efforts related to cell and gene therapy processing activities within the GMP manufacturing suite. This individual works collaboratively with manufacturing, development, and quality teams to develop extensive knowledge of cell culture processes and compliance requirements. The Associate Manager is accountable for the timely resolution of investigations and drives proactive and corrective improvements within the operation.
Responsibilities will include, but are not limited to, the following:
Knowledge And Skills
Adaptable to dynamic conditions, work practices, and project timelines.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.
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Celgene is a global biopharmaceutical company committed to improving the lives of patients worldwide. At Celgene, we seek to deliver truly innovative and life-changing treatments for our patients.