Offer summary
Qualifications:
Bachelor's degree plus five years experience, or, Master's degree plus three years experience, or, Doctorate plus two years experience., Practical radiochemistry and GMP experience required., Experience with alpha-emitting radionuclides required..
Key responsabilities:
- Manage development of manufacturing and QC procedures.
- Support regulatory filings for clinical-stage assets.
- Generate development protocols and reports.
- Participate in optimization for commercial supply.
- Interface with stakeholders including external CMOs.