- Merck (North Wales, PA)
- …Under direction from a Director, the Associate Principal Scientist is responsible for implementing regulatory strategies for our organization in ... **Job Description** This Associate Principal Scientist position... will lead the development and the implementation of regulatory strategies for their assigned projects and provide mentoring… more
- Organon & Co. (Jersey City, NJ)
- …project teams and alliance partners to develop and implement world-wide regulatory strategies for assigned biosimilar projects, with a specific focus on ... Regulatory CMC (Chemistry, Manufacturing, and Controls) requirements. This role...development due diligence activities. **Responsibilities** + Provide global strategic regulatory CMC overview for respective products and portfolio. +… more
- 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
- Astrix Technology (North Wales, PA)
- ** Associate Principal Scientist (Epidemiology)** Clinical North Wales, PA, US Pay Rate Low: 58.67 | Pay Rate High: 71.43 + Added - 14/04/2025 Apply for Job ... and innovative animal-health products, is in search of an Associate Principal Scientist to join...selection of an appropriate endpoint measure to satisfy both regulatory and reimbursement needs + Coordinate COA/PRO related sections… more
- Merck (Rahway, NJ)
- **Job Description** **Device Development Associate Principal Scientist - Development Strategy, Design Controls** **( Associate Director Equivalent)** _Our ... to ensure they are developed and manufactured in accordance with regulatory , company, and customer requirements. ** Principal Responsibilities** + Lead/contribute… more
- Merck (Rahway, NJ)
- …technical responsibility and leadership of internal and external work. The Associate Principal Scientist , Engineering position leverages scientific/technical ... to initiate, plan and execute characterization and complete technical support objectives. The scientist will be expected to exhibit a mindset of safety and quality… more
- Merck (De Soto, KS)
- **Job Description** We are seeking a highly motivated Associate Principal Scientist to join our Swine Biologicals R&D team located in De Soto, KS. The ... interact with various stakeholders including but not limited to Regulatory Affairs, Marketing, Process Development, Technical Operations, Quality Control,… 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 (Rahway, NJ)
- …energetic individual to join our Biologics Process Development Department as an Associate Principal Scientist . Applicant must have effective organizational ... cell culture processes. + Responsible for process development, process characterization, and regulatory filing activities to ensure a smooth and clear path to… more
- Merck (South San Francisco, CA)
- …Description** Our company's Research Laboratories in South San Francisco is seeking an Associate Principal Scientist with strong expertise in translational ... generation, analysis, and reporting to project teams, governance bodies, and regulatory agencies. + Drive scientific innovation and champion new enabling… more
- IQVIA (Ithaca, NY)
- **We are seeking an Associate Principal Scientist Lab Operations to join Q2 Solutions, IQVIA's laboratory business at Ithaca, NY.** **We hire passionate ... concepts in the job area. + Basic knowledge of requirements under relevant regulatory standards for the assigned work area. + Expertise in laboratory techniques. +… more
- Bristol Myers Squibb (Princeton, NJ)
- …oncology. + Manage relationships with key internal stakeholders including regulatory , clinical and commercial and scientific communications and external ... human genetics, immunology). + Minimum of 6 years post-PhD experience for Sr. Principal Level (and minimum of 8 years Post-PhD experience for AD Level), with… more
- Merck (Rahway, NJ)
- …process enhancements, next generation process development, and authoring of regulatory submissions. Under the general scientific and administrative department ... functional area on cross-functional and cross-divisional teams. + Authors required regulatory and technical documentation. Ensures that processes are developed and… 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
- Fujifilm (Thousand Oaks, CA)
- …community, and the world at large. **Job Description** **Reports to:** SeniorScientist/ Principal Scientist , Manufacturing Science and Technology **Location** : ... with and/or under the direction of a Senior or Principal Process Development Scientist . **Company Overview** Join...or PhD in Science with 1+ years of experienceor Associate degree with 6+ years of experience; or High… more
- Amgen (Thousand Oaks, CA)
- …team with varied levels of experience and report to a Process Development Principal Scientist . **Responsibilities:** + Contribute within a project team on goals ... and transform the lives of patients while transforming your career. **Process Development Associate ** **What you will do** Let's do this. Let's change the world. In… more
- Emory Healthcare/Emory University (Atlanta, GA)
- …Dermatology is seeking a highly motivated and accomplished MD/PhD or PhD scientist with experience in translational science, human subjects research, and team ... leadership to serve as Associate Director of Research Projects. This position is integral...of research projects, ensuring compliance with study protocols and regulatory requirements. + Facilitate medical student engagement in departmental… more
- UCLA Health (Los Angeles, CA)
- Description We are seeking to hire a full-time Staff Research Associate I (SRA I) in a cutting-edge gynecologic oncology research laboratory under the mentorship of ... communicate effectively on a one-to-one basis sufficiently to convey experimental results to principal investigators. + Ability to take direction as well as to work… more
- University of Colorado (Aurora, CO)
- …build a track record towards more of an independent research career as a team scientist or as a principal investigator or continue to advance their own ... application of these in new settings. **Research Mission:** + Serve as Principal Investigator (PI), Co-PI, or co-investigator on research projects and experiments to… more
- Merck (Rahway, NJ)
- **Job Description** The Senior Director (Sr. Principal Scientist ) has primary responsibility for the planning and directing clinical research activities ... including development strategy, study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication. **Specifically, the Senior Director May… more
Related Job Searches:
Associate,
Associate Principal Scientist,
Principal,
Principal Associate,
Principal Scientist,
Regulatory,
Regulatory Scientist,
Scientist