- ThermoFisher Scientific (Chelmsford, MA)
- …Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Laboratory Setting, Office, Some degree of PPE ... Position will support the BioProduction Group (BPG). **Discover Impactful Work:** The Scientist II will make an impact by driving raw material second-sourcing… more
- Takeda Pharmaceuticals (Boston, MA)
- …of my knowledge. **Job Description** **About the role:** Join as a Digital CMC Scientist to support the planning, development and execution of the In Sillico First ... Data Engineering, Computational Process Development, Systems Biology, and Advanced Process Control . + Support projects, primarily within a framework of the… more
- Amgen (Cambridge, MA)
- …formulation development, fill-finish process engineering, technical transfers to global manufacturing sites, statistical process control (SPC), and statistical ... and transform the lives of patients while transforming your career. Process Development Sr Scientist **What you will do** Let's do this. Let's change the world. In… more
- AbbVie (Cambridge, MA)
- …markets. + Lead across functions within project teams to deliver robust control strategies for starting materials, intermediates, drug substances and drug products. ... development, testing procedures, justifying specifications, and implementation of analytical control strategies to help the advancement of candidate molecules. +… more
- AbbVie (Boston, MA)
- …Description Purpose: Support regulatory approval of biologics drug substances by authoring Chemistry , Manufacturing , and Controls (CMC) filing content and by ... into regulatory documents. + Lead CMC teams in the development of robust control strategies and presentation of Control Strategy Reviews (CSRs) + Drive… more
- Merck (Cambridge, MA)
- …and Bioanalytics (PDMB) department of Research Laboratories is seeking a Senior Scientist specializing in AI/ML to support efforts in transforming the way PDMB ... implementing, and optimizing GenAI approaches to streamline the creation and quality control (QC) of regulatory submission documents. The candidate will be part of… more