- AbbVie (Worcester, MA)
- …8, Masters with 6, or PhD with 3 years of CMC biologics functional experience. + Senior Manager : Bachelors with 10, Masters with 8, or PhD with 5 years of ... that are compliant with global regulatory requirements. Partners with CMC teams during the development of CMC ...with CMC teams during the development of CMC control strategies. Implement well-defined, efficient processes for preparation… more
- Otsuka America Pharmaceutical Inc. (Providence, RI)
- …with members of the global regulatory team (GRL, regional leads, CMC -RA, labeling, medical writing, regulatory operations, etc.) to develop global regulatory ... plans, address global regulatory issues, health authority queries, and regulatory obligations. - Authors, coordinates, reviews, and executes submissions and responses to regulatory authorities related to INDs, amendments, supplements, aggregate reports, NDAs… more
- AbbVie (Worcester, MA)
- …and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The MES Program Manager is an experienced leader responsible for managing large global projects ... among projects. + Effectively communicate and present project status to Operations senior management and stakeholders + Accountable for setting program and project… more
- BD (Becton, Dickinson and Company) (Warwick, RI)
- **Job Description Summary** The Senior Regulatory Affairs (RA) Specialist within the BD Interventional Surgical Devices Business unit will work on regulatory ... antiseptic products. Under the mentorship of the Sr. RA Manager of Regulatory Affairs, they are responsible for the...required to market medical devices in the US The Senior RA Specialist will also support related regulatory affairs… more