The position is responsible for analytical testing laboratory investigation, method transfer, method improvement, remediation and/or troubleshooting for commercial products (drug substance and drug product), and Contract Service Providers (CSPs) coordination. The position involves maintaining a laboratory in compliance with safety and cGMP requirements, generating/reviewing analytical data, writing analytical documents, mentoring junior staffs, communicating with internal and external commercial product testing labs and customers, representing the team in projects as an Subject Matter Expert, and supporting cross-function initiatives. The position holder needs to exhibit strong hands-on laboratory skills, problem-solving ability/mentality, good oral/written communication skills, and scientific expertise in the characterization of pharmaceutical drug substance and drug product.
Responsibilities will include, but are not limited to, the following:
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.