- Merck (Rahway, NJ)
- …seeking a highly motivated and experienced Anatomic Pathologist (MD) for the role of Principal Scientist ( Director ) to join our innovative team. This ... and advancing digital pathology within our company's clinical therapeutic pipeline. **The** ** Principal Scientist ( Director )** **will have the following… more
- AbbVie (North Chicago, IL)
- …LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description Purpose: The Senior Principal Research Scientist / Director of Drug Metabolism and ... of absorption, distribution, metabolism, excretion (ADME), and pharmacokinetics. + Ensure regulatory compliance for all studies and reports, providing oversight of… more
- Bristol Myers Squibb (Cambridge, MA)
- …track record of high-quality scientific publications in relevant fields For the Sr. Principal Scientist position, the starting compensation for this job is a ... oncology. + Manage relationships with key internal stakeholders including regulatory , clinical and commercial and scientific communications and external… more
- Gilead Sciences, Inc. (Foster City, CA)
- …Join Gilead and help create possible, together. **Job Description** The Associate Director / Principal Scientist , Cell Culture Process Development (Pivotal & ... development, platform process evolution, and to support cell culture-related regulatory documentation. **Key Responsibilities:** + Optimize and characterize cell… more
- Merck (Rahway, NJ)
- …**Role Summary** + Under the guidance of a senior leader, a Senior Principal Scientist /Senior Director , has primary responsibility for developing value ... to reimbursement and market access, and provides input into clinical, regulatory , payer/access, marketing and evidence generation strategies and programs + In… more
- Catalent Pharma Solutions (Baltimore, MD)
- …on Quality by Design principles and regulatory compliance. The Principal Scientist will report to the Senior Director of Analytical Development and is ... ** Principal Scientist , Analytical Development** **Summary:** Catalent...Scientist - Analytical Development will report to the Senior Director , Analytical Development. **Catalent is committed to a Patient… 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
- J&J Family of Companies (Cincinnati, OH)
- …America **Job Description:** We are searching for the best talent for a Principal Scientist /Project Leader located in Cincinnati, OH. Purpose: The Principal ... necessary to competitively position products for domestic and international regulatory approval and clinical adoption. The individual will independently design,… 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)
- …and pipeline products to produce safe, effective, innovative medicine. The Senior Principal Scientist /Senior Director is responsible for protocol development ... of manuscripts for publication in peer-reviewed journals. The Senior Director will also contribute to establishing Vaccine Clinical Development Strategies… more
- UTMB Health (Galveston, TX)
- Regulatory Scientist I / II - Institutional Office... Scientist II will be assigned as a Study Director , as defined by the US FDA Good Laboratory Practice ... for the interpretation, documentation and reporting of results. The Regulatory Scientist I / II works in...I / II works in conjunction with the Scientific Director for the Institutional Office of Regulated Nonclinical Studies… more
- Honeywell (Buffalo, NY)
- As a Principal R&D Engineer/ Scientist here at Honeywell, you will play a crucial role in driving innovation and leading research and development initiatives ... mentor a team of engineers and scientists. You will report directly to our R&D Director and you'll work out of our Buffalo, NY location on a hybrid work schedule.… more
- AbbVie (Cambridge, MA)
- …more than 170 countries. Analytical Research and Development is seeking a Director (oral) Peptides to conduct process research and formulation development of ... drug substance and drug product development. + Experience developing global regulatory strategies including authoring regulatory submissions, and responding to… more
- AbbVie (Irvine, CA)
- …Science & Technology (PDS&T) - Biologics organization supports manufacturing, regulatory submission, and continuous improvement for late-stage and commercial ... opportunity for a group leader position based in Irvine, CA reporting to the Director of PDS&T Toxins. The Toxins group within the Product Development, Science &… 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
- Lilly (Indianapolis, IN)
- …respective functions but will be coordinated by the Ramp Team Sr. Director . **Key Responsibilities:** Responsible for depth of Small Molecule synthesis knowledge ... strategy effectiveness. Provide proficient data analysis and conclusions considering technical, Regulatory and Quality compliance, and business needs. + Work closely… more
- USAA (Tampa, FL)
- …of what truly makes us special and impactful. **The Opportunity** As a dedicated Director , Data Scientist , you will lead a team of Data Scientists responsible ... team's model inventory and ensures compliance with USAA model risk policies and regulatory expectations. The person will be responsible for influencing the future of… more
- UTMB Health (Galveston, TX)
- …utilize the US FDA GLP regulations as a reference standard. The Regulatory Scientist II may also function as a Principal Investigator for extramurally funded ... Select Agent Program (FSAP). **JOB SUMMARY** **Function** : The Regulatory Scientist II will be assigned as...Scientist II will be assigned as a Study Director , as defined by the US FDA Good Laboratory… more
- Sutter Health (San Francisco, CA)
- …as periodically summarizing QC and PT results in reports or graphs for Medical Director review. Also performs a variety of Quality Assurance (QA) duties such as ... in maintaining accreditation readiness; participates in accreditation surveys and regulatory agency inspections. Advises on, and provides guidance for, technical… more
- Eurofins (Columbia, MO)
- …relationships, and reactions of matter. + May assist or serve as study director , principal investigator, or project leader for GLP studies. May assist ... colleagues with constructive feedback. Eurofins Agroscience Services is searching for an Assistant Scientist I, Residue to work in Columbia, MO. This is an entry… more
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