- Mizuho Corporate Bank (New York, NY)
- …testing including reviewing the approach, testing and reports for issues (eg regulatory , third-party and internal audit) related to credit risk.In accordance with ... of key business strategies and regulations. Continuously scan the business, regulatory and financial environments for emerging and critical issues affecting the… more
- MEAG Power (Atlanta, GA)
- …MEAG generation fleet, including acquiring fuel and ensuring compliance with all regulatory requirements. Controls and manages all day to day activities associated ... a timely manner. Provide input and influence of new regulatory requirements in all areas working with industry trades,...federal, state or local laws. MEAG Power is a drug -free workplace. External candidates are required to pass a… more
- AbbVie (North Chicago, IL)
- …the impact on Operations. + Understand and present technical information regarding drug product and drug substance manufacturing processes and methods, process ... development/history and process characterization to senior management and regulatory agencies. + Prepare and review submissions through registration of the product… more
- Amgen (Thousand Oaks, CA)
- …scientific strategy and planning and execution for all aspects of clinical drug development across Amgen's clinical programs. This Executive Director within Clinical ... Development will be involved with the full scope of the rare disease clinical drug development activities from the design and execution of Phase 2 through Phase 4… more
- University of Michigan (Ann Arbor, MI)
- …clinical study supply organization and clinic room preparation. + Manage regulatory requirements including IRB submissions in eResearch Regulatory Management ... Some familiarity with REDCap, OnCore, Epic, MiCHART, and eResearch applications + IRB/ regulatory experience **Modes of Work** Positions that are eligible for hybrid… more
- Bristol Myers Squibb (Madison, NJ)
- …the design, execution, and interpretation of studies to select the most promising drug candidates for later development. **Position Summary / Objective** + Serves as ... data to support development + Serving as principal functional author for Regulatory submission, study reports, and publications + Provides oversight and medical… more
- Merck (Wilson, NC)
- …(eg temperature monitors). To provide SME guidance in support of small molecule drug substance and drug product container closure systems including mold ... qualification and regulatory compliance. To act as master data stewards and...across the end to end supply chain, and analytical, regulatory , and project leaders. The successful candidate will demonstrate… more
- Stantec (Roseville, CA)
- …and studies, including environmental remediation and restoration. - EHS regulatory compliance assessments and audits at industrial and manufacturing client ... and/or state environmental regulations. - Technical consulting for clients on regulatory compliance matters including permit management, routine regulatory … more
- Lilly (IN)
- …consultative support to product teams, internal Lilly partners, external organizations, regulatory agencies and external partners on medical and scientific issues. ... and dose finding studies, as well as authoring of regulatory documents. You will act as a scientific and...clinical trial efficacy and safety data + Knowledge of drug development process + Excellent communication skills, both verbal… more
- Lilly (Indianapolis, IN)
- …Plan, database, and observed datasets) + Support submission, inspection and regulatory response activities + Lead cross Business Unit/Therapeutic Area projects or ... data + Effectively apply knowledge of applicable internal, external and regulatory requirements/expectations (MQA, CSQ, MHRA, FDA, ICH, GCP, PhRMA, Privacy… more