- ThermoFisher Scientific (Indianapolis, IN)
- …including dossier development and submissions, in collaboration with Medical & Scientific Affairs and Market Access colleagues. + Provide support and guidance to ... early-stage program teams with various RWE activities to optimize clinical...well as emerging HEOR/RWE methodologies and applications. + Communicate regulatory with internal and external stakeholders to ensure all… more
- J&J Family of Companies (Indianapolis, IN)
- …As a valued member of the MedTech Product Stewardship organization under the Global Regulatory Affairs organization, she/he can be located at any J&J MedTech ... Program Manager, Emerging Risks & Impact Assessments (MedTech)...States **Organization** Medical Devices & Diagnostics Global Services, LLC (6209) **Job Function** Regulatory Affairs **Req ID:**… more
- Corteva Agriscience (Indianapolis, IN)
- …in the Corteva portfolio. This role will work closely with Corteva Government Affairs and Industry Affairs colleagues to support policy outcomes that support ... desired business outcomes. A thorough knowledge of public affairs as a discipline would therefore be helpful. This role will work cross-functionally to provide… more
- Sumitomo Pharma (Indianapolis, IN)
- …changes to contract manufacturing organizations, testing laboratories, clinical sites and regulatory affairs as needed. + Responsible for compliance with ... Director ensures compliance with GMPs, SMPA procedures and applicable global Regulatory guidelines by providing oversight and management of the global contract… more
- WM (Danville, IN)
- …Management Trainee (DOMT) position is part of a required developmental training program lasting up to 18 months.** The duties and responsibilities are under ... leachate management, and waste streams and sales. The Disposal OMT training program is designed to develop individuals into Operations Managers and District Managers… more
- Lilly (Indianapolis, IN)
- …operate across many corporate functions including Global Patient Safety (GPS), Global Regulatory Affairs (GRA), Clinical Design, Delivery and Analytics (CDDA), ... Organization (MQO) is for the design, implementation, and execution of a medical, regulatory , and safety quality system to support the evolving cell and gene therapy… more
- Prime Therapeutics (Indianapolis, IN)
- …written and verbal communication skills with the demonstrated ability of presenting program and project updates to senior executives + Strong organizational, ... to drive synergies related to quality improvement and new product / program development for Prime's Government Programs book of business. Provide strategic… more