- ThermoFisher Scientific (Plainville, MA)
- …and drive efficiency throughout the organization. + Support internal, external, and regulatory inspections as needed. + Hire and develop employees within the ... actions. + Serve as primary QC Bioanalytical contact for regulatory inspections and client audits. + Provide support for...BS required, MS preferred in a scientific/technical field. + PhD in a scientific/technical field is a plus. **Experience**… more
- Sanofi Group (Cambridge, MA)
- …of sanofi revenues by expediting submission timelines and facilitating reviews by regulatory agencies of sanofi key assets. + He/she: Creates and executes a ... + Utilizes creative, thoughtful and boundary-pushing strategies, and performs risk analysis , to propose and lead organizational and process transformations to… more
- Bristol Myers Squibb (Cambridge, MA)
- …TLs to address nonclinical translational questions + Participates in post-hoc biomarker analysis and publication efforts + Supports regulatory submissions and ... up biomarker plans for individual trials and ensuring appropriate collection and timely analysis and reporting of final biomarker data. The individual will also be… more
- Bristol Myers Squibb (Devens, MA)
- …fate/effects studies and environmental risk assessments according to appropriate international regulatory guidelines. This role will lead and participate on diverse ... risk assessments and environmental fate/effects studies focused on global regulatory frameworks, technical knowledge and emerging scientific trends; Lead matrix… more
- Bristol Myers Squibb (Boston, MA)
- …on translational data generated to support asset development and contribute to regulatory submissions. This individual will work on cross-functional project teams to ... scientists, as well as BMS members from clinical, medical, commercial, regulatory , and diagnostics. Individual will also engage with external academic… more
- Charles River Laboratories (Shrewsbury, MA)
- …management, interpretation, and reporting of study data and assuring the regulatory compliance of these projects, as appropriate. Additional responsibilities include ... responsible for the composition and execution of validation and sample analysis protocols/plan in accordance with company standard operating procedures and industry… more
- Sanofi Group (Waltham, MA)
- …the mRNA technology platform **About You** **Experience:** + Minimum requirements (Sr. Engineer level): PhD with 4+ years, MS with 6+ years, or BS with 8+ years of ... to and in a GMP environment + Knowledge of regulatory requirements for process changes and technology implementation +...concepts into practical applications + Background in modeling, data analysis , or automation is a plus **Soft Skills** +… more
- Bristol Myers Squibb (Cambridge, MA)
- …activities for the pipeline and supports late stage portfolio for regulatory , translational development and life cycle management. Translational Development drives ... teamwork and contribute to project strategy discussions. **Qualifications** + For Scientist level, PhD with at least 2 years of relevant work experience. + For… more
- General Atomics (Boston, MA)
- …**Job Qualifications:** + Typically requires a bachelors degree, masters degree or PhD in engineering or a related technical discipline from an accredited ... masters degree, or seven or more years with a PhD . May substitute equivalent engineering experience in lieu of...and other essential tools for precise antenna testing and analysis + Ability to work with and manage subcontractors,… more
- Sanofi Group (Cambridge, MA)
- …to inform and shape decision making by senior leadership (eg, stage gate analysis to determine optimal development strategy, scenario analysis , decision trees, ... for pipeline development and positioning. + Drive strategic questions and analysis and synthesize results to support project-level and portfolio-level decision… more