- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Associate Principal Scientist of Device Technology Assessment and Early Development will spearhead early-stage device technology ... device and/or combination product space.In-depth knowledge of medical device development, regulatory requirements, and quality standards, with a proven track record… more
- Merck & Co. (Rahway, NJ)
- …& Product Modeling Team in our Company Manufacturing Division seeks an experienced Associate Principal Scientist who will develop and utilize advanced ... and cGMP environments is highly desired. Familiarity or experience with regulatory filings (BLAs, NDAs) and CMC processes preferred.Experience with high-performance… more
- Merck & Co. (Rahway, NJ)
- …products and processes are developed in accordance with applicable regulatory , quality, company, and customer requirements.-This position will lead cross-functional ... and influence clinical and commercial combination product development and launches. Principal ResponsibilitiesLead and set direction for the device development… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Senior Clinical Director (Sr. Principal Scientist ) has primary responsibility for the strategic planning and directing clinical research ... pursue and subsequent study design, initiation, execution, monitoring, analysis, regulatory filing, and publication. Specifically, The Senior Clinical Director May… more
- System One (Rahway, NJ)
- Job Title: Associate Principal Scientist , Regulatory Affairs Location: Rahway, NJ (Hybrid) Hours/Schedule: Mon- Fri; 8am- 5pm Type: Contract ... Responsibilities The Associate Principal Scientist is responsible for developing CMC regulatory submission strategies and timelines for assigned… more
- Merck (Rahway, NJ)
- **Job Description** The Associate Principal Scientist , General Medicine Publications Medical Writing, works with scientists in our company's Research Labs ... other of our Research & Development Division science. The Associate Principal Scientist is expected...Translational Medicine, Global Medical and Scientific Affairs, and Global Regulatory Affairs and Clinical Safety to identify key issues… more
- Merck (Rahway, NJ)
- **Job Description** The Associate Principal Scientist of Device Technology Assessment and Early Development will spearhead early-stage device technology ... and/or combination product space. + In-depth knowledge of medical device development, regulatory requirements, and quality standards, with a proven track record of… more
- Merck (Rahway, NJ)
- …& Product Modeling Team in our Company Manufacturing Division seeks an experienced Associate Principal Scientist who will develop and utilize advanced ... and cGMP environments is highly desired. Familiarity or experience with regulatory filings (BLAs, NDAs) and CMC processes preferred. + Experience with… more
- Merck (Rahway, NJ)
- …ensure products and processes are developed in accordance with applicable regulatory , quality, company, and customer requirements. This position will lead ... and influence clinical and commercial combination product development and launches. ** Principal Responsibilities** + Lead and set direction for the device… more
- Merck (Rahway, NJ)
- …art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for ... the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support. The incumbent is responsible for… more
- Merck (Rahway, NJ)
- **Job Description** The **Senior Clinical Director (Sr. Principal Scientist )** has primary responsibility for the strategic planning and directing clinical ... pursue and subsequent study design, initiation, execution, monitoring, analysis, regulatory filing, and publication. **Specifically, The Senior Clinical Director May… more
