- Merck (Rahway, NJ)
- …Director , Combination Product Regulatory CMC - (R5)** This Principal Scientist position is equivalent to a Director position. Under direction from the ... Combination Product Regulatory CMC Team Leader, the Principal Scientist is responsible for executing in the Regulatory CMC space. Leveraging demonstrated… more
- Merck (Rahway, NJ)
- … updates. + Audit vendors/partners of SaMD/IVD/Companion Diagnostics **Reports to** - Director Regulatory Compliance, Device Quality and Regulatory ... This position will be part of the Device Quality & Regulatory Team within Global Regulatory Affairs and Clinical Safety (GRACS). The primary responsibility for… more
- Merck (Rahway, NJ)
- **Job Description** ** Principal Scientist , Small Molecule Analytical Research & Development** The Small Molecule Analytical Research and Development (SMAR&D) ... group has an exciting opportunity for a Principal Scientist based in Rahway, NJ. Join...sterile and combination products. You will also contribute towards regulatory submissions to enable clinical trials. Your main responsibilities… more
- Merck (Rahway, NJ)
- **Job Description** The Director ( Principal Scientist ) has primary responsibility for the planning and directing clinical research activities involving new ... cycle of clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and publication. **Specifically, The Director May… more
- Merck (Rahway, NJ)
- …of our company's Research Laboratories Division is seeking applicants for a Principal Scientist position available at our company's 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 of scientists… more
- Merck (Rahway, NJ)
- …process validation, second generation process development and authoring of regulatory submissions. Under the general scientific and administrative direction of ... the Director in Biologics Cell Culture Sciences group and working...next generation process development and characterization, process validation, and regulatory submission authoring **In this role, the successful candidate… more
- ThermoFisher Scientific (New Brunswick, NJ)
- …and Drug Products across internal and external manufacturing sites. The principal scientist reports to the Associate Director of GBS and is responsible for ... stability protocols, and preparation, review and approval of CMC elements of regulatory filings to support the activities of the Global Biologics Stability program… more
- City of New York (New York, NY)
- …compliance, and capital projects engineering and construction review and approval. Provide principal regulatory oversight and sanitary survey for the NYC ... including program management, resource allocation. Key program activities include regulatory inspections, issuance of commissioner's orders, bathing establishments engineering… more
- Bristol Myers Squibb (Madison, NJ)
- …acting on Clinical Trial data to support development, and + Serving as principal functional author for Regulatory submission, study reports, and publications + ... at work and in their personal lives. Read more: careers.bms.com/working-with-us . ** Director , Early Clinical Development (MD) - Hematology & Cell Therapy with Focus… more