- Merck & Co. (Rahway, NJ)
- …with talented and dedicated colleagues while developing and expanding your career.The Senior Director ( Sr . Principal Scientist ) has primary responsibility ... studiesWork closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical… more
- Merck & Co. (North Wales, PA)
- …implementation of internal regulatory strategies and provides mentoring and coaching to Sr . Scientist and Assoc Principle scientist in support of their ... divestment and product withdrawal.Support new technology development.Demonstrate an understanding of regulatory affairs and applies this understanding to the… more
- Merck & Co. (Rahway, NJ)
- …studies;Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical ... dedicated colleagues while developing and expanding your career.--The Director (Principal Scientist ) has primary responsibility for the planning and directing of… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …timelines for the assigned projects. The individual will also contribute to regulatory process optimizations on relevant topics.Responsibilities- Supports CMC ... with cross functional teams and various departments to include Marketing, Medical Affairs , Regulatory Affairs , Supply Chain Technical Operations,… more
- Merck & Co. (North Wales, PA)
- …studiesWork closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical ... colleagues while developing and expanding your career.The Clinical Director (Principal Scientist ) has primary responsibility for the planning and directing clinical… more
- ThermoFisher Scientific (Cambridge, MA)
- …+ Complete the Design and execution of experiments to support process development of advance novel vaccine programs from preclinical through clinical ... with minimal supervision, maintaining good scientific practice. + Complete process characterization studies for current program + Complete data...authoring of technical reports in collaboration with QA / RA / MSAT / ARD teams and assist in… more
- AbbVie (North Chicago, IL)
- …disciplines to further program goals via collaborations with drug product development, regulatory affairs , and commercial operations. + The candidate will ... development of AbbVie's clinical candidates. We are seeking a Principal Research Scientist II to conduct process research and development of antibody-drug… more
- Balchem (Montvale, NJ)
- Senior Scientist - Corporate Regulatory Affairs ...the Legal team as part of the claims review process . + Prepare high quality ad hoc and form ... internal customer service. Provide expert guidance to internal stakeholders on regulatory affairs as they relate to Balchem- s product lifecycle management (R&D,… more
- Organon & Co. (Jersey City, NJ)
- …the Director in Regulatory Chemistry, Manufacturing & Controls (CMC), the Senior Scientist is responsible for implementing Regulatory Chemistry, ... for assigned products in accordance with global regulations, guidance's, and defined regulatory strategies. The Senior Scientist is responsible for… more
- Lilly (Indianapolis, IN)
- …people who are determined to make life better for people around the world. ** Senior Advisor/Director, Global Regulatory Affairs - CMC, Small Molecules** At ... patients who need them all over the world. The Senior Advisor/Director in Global Regulatory Affairs...molecule portfolio, including small molecules, peptides, and oligonucleotides. The regulatory scientist will be expected to leverage… more
- Lilly (Indianapolis, IN)
- …operational support for market registrations and post-approval submissions. The regulatory scientist in Global Regulatory Affairs - CMC Biotechnology ... need them all over the world. We are seeking Regulatory Scientist GRACMC-Biotechnology to be a part...+ Demonstrated deep knowledge of the biologic drug development process . + Bioproduct Regulatory CMC experience supporting… more
- Novo Nordisk (Plainsboro, NJ)
- …designated personnel. Relationships Report to the Director/Associate Director/Lead Regulatory Scientist / Sr . Manager Regulatory Affairs . Develop and ... maintain positive rapport and working relationships with other personnel in Regulatory Affairs , CMR, and other local and headquarter departments to accomplish… more
- Herbalife (Winston Salem, NC)
- …routinely with Herbalife global cross functional teams including Quality, Strategic Sourcing, Regulatory Affairs , Project Management and Supply Chain as well as ... Sr . Research Scientist , R&D Technical Operations...position is responsible for carrying out formulation and manufacturing process qualifications for product acquisition, reformulation, technology transfer activities,… more
- Abbott (Santa Clara, CA)
- …data. + Facilitates regulatory submissions and communications by communicating with Regulatory Affairs during the submission process . Generate documents ... serve people in more than 160 countries. **Job Title** Sr . Research Scientist **Working at Abbott** At...other departments including Global Clinical Operations, Research & Development, Regulatory Affairs , and Biostatistics. + Writes, study… more
- Merck (North Wales, PA)
- …with talented and dedicated colleagues while developing and expanding your career. The Senior Director ( Sr . Principal Scientist ) has primary responsibility ... + Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development… more
- Unilever (Burlington, VT)
- …marketplaces. Claims Review & Approval + Lead claims risk discussions between Marketing, Regulatory Affairs , Research & Development, and Legal to drive decisions ... Who You Are and What You'll Do The Senior Claims & Compliance Scientist works...stakeholders, and archiving approved materials. + Work closely with Regulatory Affairs to ensure comprehensive claims review.… more
- Kelly Services (Frederick, MD)
- …prestigious research organizations in the world. We are currently seeking a Toxicology Senior Scientist with the National Institutes of Health in Rockville, MD. ... do for you at www.kellygovernmentsolutions.com POSITION SUMMARY: The Toxicology Scientist will serve as the primary toxicology subject matter...to toxicity studies as directed by the Office of Regulatory Affairs . + Attend and contribute to… more
- University of Washington (Seattle, WA)
- …noted for diversity, intellectual excitement, artistic pursuits and natural beauty. The Senior Scientist of Clinical and Regulatory Development (Research ... and optimization of high-complexity molecular and cytogenomic assays and process improvement that will be used for the Genetics...suitable to a clinical laboratory environment. + Experience in regulatory affairs in clinical diagnostics. + To… more
- Abbott (Plymouth, MN)
- …stake holders including clinical project management, clinical operations, biostatistics data management, regulatory affairs , medical affairs as well as ... 114,000 colleagues serve people in more than 160 countries. ** Senior Principal Clinical Scientist ** **Working at Abbott**...risk management, or clinical evaluation planning for products and process changes, to gain regulatory approval for… more
- Abbott (Plano, TX)
- …new applications in the field. + Experience in both materials characterization and regulatory affairs to support product approval filing and marketing. + ... people in more than 160 countries. **Job Title** : ** Senior Engineer Material Scientist , R&D - Polymers**...will work closely with advanced development, mechanical engineering, and process development teams to select the right polymers for… more
