- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Associate Principal Scientist , Device Risk Management Lead, is a crucial member of our team, responsible for spearheading risk management ... through launch and post-market surveillance. Key Responsibilities and Activities: The Associate Principal Scientist , Device System - Device Risk Management will… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionAssociate Principal Scientist - Device Technical and Engineering Lead (Associate Director Equivalent) Our company's Device Product & Process ... products and processes are developed in accordance with applicable regulatory , quality, company, and customer requirements.-This position will lead cross-functional… more
- Merck & Co. (North Wales, PA)
- …state-of-the-art technology and applying rigorous scientific and ethical standards.The Senior Director (Senior Principal Scientist ) has primary ... to provide the safety and efficacy data required for regulatory approval of potential new drugs, vaccines and new...post-licensure). With a focus on late-stage development, the Senior Director will manage the entire cycle of clinical development,… more
- Merck & Co. (Rahway, NJ)
- …department of our company Research Laboratories Division is seeking applicants for a Principal Scientist position available at its Rahway, New Jersey research ... facility. The Principal Scientist is a senior scientific role tasked with working closely with the group Director to define group strategy and to lead a team… more
- Merck & Co. (MA)
- Job DescriptionThe Senior Director (Sr. Principal Scientist ) has primary responsibility for the strategic planning and directing clinical research activities ... to pursue and subsequent study design, initiation, execution, monitoring, analysis, regulatory filing, and publication.Specifically, The Senior Director May Be… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Senior Director (Sr. Principal Scientist ) has primary responsibility for the planning and directing clinical research activities involving ... including development strategy, study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication.Specifically, the Senior Director … more
- Organon & Co. (Plymouth Meeting, PA)
- …Organon Regulatory Chemistry, Manufacturing and Controls (CMC), the Associate Principal Scientist is responsible for developing and implementing ... Description** **The Position** Reporting to the Director or Executive Director in...global regulations and guidances, and Organon procedures. The Associate Principal Scientist will lead the preparation and… more
- Merck (West Point, PA)
- **Job Description** **Associate Principal Scientist - Device Technical and Engineering Lead (Associate Director Equivalent)** _Our company's Device Product & ... ensure products and processes are developed in accordance with applicable regulatory , quality, company, and customer requirements. This position will lead… more
- Merck (West Point, PA)
- **Job Description** The Associate Principal Scientist , Device Risk Management Lead, is a crucial member of our team, responsible for spearheading risk management ... launch and post-market surveillance. **Key Responsibilities and Activities:** The Associate Principal Scientist , Device System - Device Risk Management will… more
- Merck (Rahway, NJ)
- …technology and applying rigorous scientific and ethical standards. The Senior Director (Senior Principal Scientist ) has primary responsibility ... to provide the safety and efficacy data required for regulatory approval of potential new drugs, vaccines and new...post-licensure). With a focus on late-stage development, the Senior Director will manage the entire cycle of clinical development,… more
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