$80K — $100K *
Turning Point Therapeutics (TPT) is seeking a highly motivated individual to join the CMC team as a Senior Scientist, Drug Substance Process Development. The main role is to conduct process research and development activities at Contract Development and Manufacturing Organizations (CDMOs), and to manage the manufacturing of TPT portfolio compounds. Close collaborations with Quality Control, Quality Assurance, Drug Product, and CMC Regulatory teams are required.
The successful candidate will have experience in process chemistry research and development, cGMP manufacturing, and management of CDMOs. Experience in QA/QC, as well as authoring CMC sections of regulatory documents (such as INDs, NDAs, MAAs and IMPDs) will be highly desirable.
The position reports to the Director, Drug Substance Development and Manufacturing.
EEO & Employment Eligibility
Turning Point Therapeutics 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. Turning Point Therapeutics also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Turning Point Therapeutics is an E-Verify employer.
Valid through: 11/21/2021