- Merck (West Point, PA)
- …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 (West Point, PA)
- …a healthier future for all. We have an exciting opportunity for an ** Associate ** ** Principal Scientist ** with significant experience in immunological assays ... professional development. + Properly document protocols and findings, author preclinical regulatory documents, and comply with all laboratory safety requirements. +… more
- Merck (West Point, PA)
- **Job Description** We are seeking an Associate Principal Scientist to join our Vaccine Analytical Research and Development Separations and Biochemical ... trends in industry, and preparing technical documents to support regulatory submissions. **Education Minimum Requirement:** + Ph.D. in analytical… more
- Merck (West Point, PA)
- …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 (West Point, PA)
- …and external manufacturing sites, process validation, and authoring of regulatory submissions. For commercial programs, activities include site-to-site process ... next generation process development and characterization, process validation, and regulatory submission authoring. _In this role, the successful candidate will… more
- Merck (North Wales, PA)
- …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 (Upper Gwynedd, PA)
- **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 (West Point, PA)
- **Job Description** Our Company a global healthcare leader, is seeking an Associate Principal Scientist to join our collaborative, dynamic, and inclusive ... diverse, dynamic, AAALACi-accredited animal research institution. Collaborate cross-functionally with principal investigators, scientific staff, toxicologists, pathologists, veterinarians, veterinary technicians,… more