- Merck (Madison, WI)
- …Director , Combination Product Regulatory CMC - (R5)** This Principal Scientist position is equivalent to a Director position. Under direction from the ... Combination Product Regulatory CMC Team Leader, the Principal Scientist is responsible for executing in the Regulatory CMC space. Leveraging demonstrated… more
- Merck (Austin, TX)
- … updates. + Audit vendors/partners of SaMD/IVD/Companion Diagnostics **Reports to** - Director Regulatory Compliance, Device Quality and Regulatory ... This position will be part of the Device Quality & Regulatory Team within Global Regulatory Affairs and Clinical Safety (GRACS). The primary responsibility for… 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
- 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)
- …to reimbursement and market access, and provide input into clinical, regulatory , payer/access, marketing and evidence generation strategies and programs. + In ... collaboration with internal teams and external partners, design studies, author study protocols, develop measurement questionnaires, case report forms, data analysis plans, final study reports, scientific presentations, and publications. + Responsible for… 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
- Merck (Rahway, NJ)
- **Job Description** The Director ( Principal Scientist ) has primary responsibility for the planning and directing clinical research activities involving new ... cycle of clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and publication. **Specifically, The Director May… more
- MD Anderson Cancer Center (Houston, TX)
- …undergraduate and graduate students, trainees, professionals, employees, and the public. The Principal Research Scientist for the Proteomics Core will provide ... in the Proteomics core in alignment with the Core Director 's vision and strategic goals. *Key Functions * 1....1. Assist in developing scientific planning and financial and regulatory oversight of the Proteomics Core Facility. 2. Monitor… 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
- USAA (Charlotte, NC)
- …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
- Charles River Laboratories (Mattawan, MI)
- …participate in process improvement initiatives, and may function as a Principal Investigator or Study Director . **Job Qualifications** The following ... education are added correctly. **Job Summary** We are seeking an **Senior Associate Scientist ** for our **Bioanalytical Team** site located in **Mattawan, MI** . The… 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
- Charles River Laboratories (Cleveland, OH)
- …studies + Independently function as a Principal Investigator, Individual Scientist and/or Study Director Essential Duties and Responsibilities: continued + ... that you can feel passionate about. **Job Summary** We are seeking a Research Scientist I - Method Development for our Bioanalytical Chemistry team for our Safety… more
- Charles River Laboratories (Cleveland, OH)
- …with minimal oversight + Function as a Principal Investigator, Individual Scientist and/or Study Director as assigned with minimal oversight + Actively ... about. **Job Summary** We are seeking a Senior Associate Scientist for our Manual Ion Channel Testing team at...observations + Assist in problem solving for technical and/or regulatory issues with oversight + Responsible for writing and… more