
Regulatory Affairs Lead: IVDs & Global Submissions
Roche, indianapolis, in, United States
A global healthcare leader is seeking a Regulatory Affairs Manager in Indianapolis to oversee IVD development and manage regulatory submissions. The ideal candidate will hold an advanced degree in Life Sciences and have extensive experience in regulatory affairs, especially with IVDs and CLIA regulations. Responsibilities include developing registration dossiers and collaborating with various stakeholders to navigate complex regulatory challenges. The role offers a competitive salary package based on qualifications and experience.
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