- Merck (Rahway, NJ)
- …biologics, and pharmaceutical products and combination products. We are seeking an experienced Associate Principal Scientist to advance and commercialize an ... to internal and external sites, process validation, authoring of regulatory submissions and support of significant manufacturing investigations. The...a member of the ADC drug product team, the Associate Principal Scientist will have… more
- Merck (Rahway, NJ)
- …knowledge in both analytical experimental design and biotherapeutic pipeline programs. Finally, this Associate Principal Scientist will be a partner in ... Mass Spectrometry -group in Rahway, NJ is seeking a motivated scientist with technical expertise in mass spectrometry-based protein characterization. This position… 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)
- …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 **Clinical Director ( Principal Scientist )** has primary responsibility for the strategic planning and directing clinical research ... to pursue and subsequent study design, initiation, execution, monitoring, analysis, regulatory filing, and publication. **Specifically, The Clinical Director May Be… more
- Merck (Rahway, NJ)
- **Job Description** ** Associate Principal Scientist , Biologics Analytical Research & Development** Our Research Scientists are our Inventors. We identify and ... department of our Research & Development Division is seeking applicants for an Associate Principal Scientist position available at its Kenilworth, New… more
- Atlantic Health System (Pompton Plains, NJ)
- …Care Testing program in various clinical departments, ensuring compliance with regulatory standards, and promoting patient safety. Principal Accountabilities: + ... Follow POCT policies, procedures, and guidelines in accordance with regulatory requirements. + Assist on maintaining adequate supply of materials for test procedures… more
- Atlantic Health System (Summit, NJ)
- …obtain data for use in the diagnosis and treatment of disease. Principal Accountabilities: 1. Demonstrates proficiency and follows testing procedures and policies by ... revision of procedures and documentation related to accreditation, adhering to all regulatory requirements for various authorities, including but not limited to CAP,… more