- Organon & Co. (Plymouth Meeting, PA)
- …the Director or Executive Director in Organon Regulatory CMC New Products, the Associate Principal Scientist ( Associate Director) is responsible for ... and will encompass late-stage development products and commercially approved compounds. The Associate Principal Scientist may also support project team… more
- Merck (Upper Gwynedd, PA)
- **Job Description** We are seeking a Director ( Principal Scientist ), Global Regulatory Affairs Liaison with a visionary, growth-oriented mindset that can ... our pipeline and drive our strategic priorities. The Director, Principal Scientist | Regulatory Affairs...labeling and obtain shortest time to approval by global regulatory agencies. + Reports to Associate Vice… more
- Merck (West Point, PA)
- …growing pipeline of diverse products and evolving technologies. We are seeking an Associate Principal Scientist to advance and commercialize the intravitreal ... to internal and external sites, process validation, authoring of regulatory submissions and support of significant manufacturing investigations. The...As a member of the drug product team, the Associate Principal Scientist will be… more
- Merck (West Point, PA)
- …the growing pipeline of diverse products and evolving technologies. We are seeking an Associate Principal Scientist who is an experienced drug product ... transfer to internal and external sites, process validation, authoring of regulatory submissions and support of significant manufacturing investigations. The group… more
- Merck (West Point, PA)
- **Job Description** Associate Principal Scientist to support mutagenic and non-mutagenic risk assessment activities as well as perform in silico assessments ... group within the Nonclinical Drug Safety organization is seeking an office-based scientist with expertise in impurity risk assessment. A core responsibility will be… 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
- Bristol Myers Squibb (Princeton, NJ)
- …difference. **Summary/Scope** Reporting to Senior Scientific Director Translational Medicine, the TM Sr. Principal Scientist will be part of the late stage TM ... Participates in post-hoc biomarker analysis and publication efforts + Supports regulatory submissions and regulatory interactions as needed **Skills/Knowledge… more
- J&J Family of Companies (Fort Washington, PA)
- Principal Scientist , Self-Care R&D - 2407026709W **Description** ** Principal Scientist - Self-Care Product and Process Development** **Location:** ... the scientists of the future. We are seeking a highly skilled and experienced Principal Scientist to join our Self-Care Product and Process Development team.… more
- Bristol Myers Squibb (Princeton, NJ)
- …. **Summary/Scope** Reporting to Senior Scientific Director Translational Medicine (TM), the TM Associate Director will be part of the late stage TM group. The ... Participates in post-hoc biomarker analysis and publication efforts + Supports regulatory submissions and regulatory interactions as needed **Skills/Knowledge… 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 (North Wales, PA)
- …data + Produce tables and graphics for inclusion in study reports and regulatory submissions + Ensure programmatic traceability from data source to modeling result + ... + produce SAS transport files and associated documentation for regulatory submissions + Represent statistical programming on process improvement activities… 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 ... Data Repositories. + United States and/or worldwide drug or vaccine regulatory application submission experience at the leadership level including the development… more
- Merck (West Point, PA)
- …Product Development (VDPD), a part of our company's Research Laboratories, is seeking an Associate Principal Scientist to join our department in West Point, ... root cause analysis and investigations (FMEA, fishbone, etc.) + Experience authoring regulatory filings for sterile dosage forms (adjuvants and/or DP) + Experience… 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
- Merck (North Wales, PA)
- …while developing and expanding your career. The Senior Clinical Director (Sr. Principal Scientist ) has primary responsibility for the planning and directing ... of clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and publication. **Specifically, the Senior Director may be… more