- Merck & Co. (Rahway, NJ)
- …within the Device Development team and with external partners.Understand and apply regulatory and compliance requirements relevant to device risk management ... Job DescriptionThe Associate Principal Scientist, Device Risk Management Lead, is a...control measures, and performing overall device risk evaluations in compliance with ISO 14971 and other relevant standards. Ensure… more
- Merck & Co. (Rahway, NJ)
- …DESCRIPTION SUMMARY Primary activities include but are not limited to: The Associate Principal Scientist is a DVM and/or PhD whose primary function is to design, ... and report clinical laboratory and field studies that will support the regulatory approval of new companion animal and livestock products. The position requires… more
- Merck & Co. (Rahway, NJ)
- …of our company Research Laboratories Division is seeking applicants for a Principal Scientist position available at its Rahway, New Jersey research facility. The ... Principal Scientist is a senior scientific role tasked with...- Authoring and reviewing internal technical reports, sections of regulatory filings ( eg, IND , BLA ) and… more
- Merck & Co. (Rahway, NJ)
- …to ensure they are developed and manufactured in accordance with regulatory , company, and customer requirements. - Principal Responsibilities Lead/Support ... to improve processes related to device-drug integration. Partner with Quality and Regulatory teams to ensure compliance with applicable global regulations.… more
- Merck & Co. (Boston, MA)
- …Intellectual Curiosity, Interdisciplinary Problem Solving, Medical Research, Pharmacovigilance, Regulatory Compliance , Regulatory Reporting, Scientific ... teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new drugs, vaccines and new indications for existing… more
- Merck & Co. (North Wales, PA)
- …Research, Pain Management, Pharmaceutical Development, Regulatory Affairs Compliance , Regulatory Compliance , Scientific Leadership, Scientific ... teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new drugs, vaccines and new indications for existing… more
- Merck & Co. (South San Francisco, CA)
- Job Description Senior Principal Scientist Translational Medicine, Immunology Translational Medicine in our Research & Development Division is responsible for ... point in the drug development process, working closely with scientific, regulatory , statistical, and modelling colleagues across the organization to translate the… more
- Merck & Co. (Rahway, NJ)
- …Microbial Fermentation, Process Analytical Technology (PAT), Process Scale Up, Regulatory Compliance , Scientific Innovation, Strategic Leadership, Strategy ... Job DescriptionThe Microbial Process Operations (MPO) Team is seeking a Senior Principal Scientist with expertise in microbial process development for the production… more
- Merck & Co. (South San Francisco, CA)
- …Dynamics, Metabolism and Bioanalytics (PDMB) group is seeking an Associate Principal Scientist to contribute to our Company's biologics, drug conjugates, and ... novel modality discovery and development pipeline. The Associate Principal Scientist will be primarily discovery team-facing and is expected to be a key contributor… more
- Merck & Co. (MA)
- …Drug Development, Gastroenterology, Inflammatory Bowel Diseases, Pharmaceutical Industry, Regulatory Compliance , RheumatologyPreferred Skills: Current Employees ... Job DescriptionThe Senior Director (Sr. Principal Scientist) has primary responsibility for the strategic planning and directing clinical research activities… more
- Merck & Co. (North Wales, PA)
- …Data Analysis, Data Management, Data Science, Numerical Analysis, Project Management, Regulatory Compliance , Regulatory Requirements, Scientific Leadership, ... art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Principal Scientist, Drug Discovery in our Research and Development Department will be responsible for identifying new molecular entities and ... cardiology, pain & inflammation, reproduction, drug delivery or biotechnologyKnowledge of regulatory aspects of pharmaceuticals including GLP, GCP and GMPAbility to… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionSr. Principal Scientist - Device Technical and Engineering Lead (Sr. Director Equivalent)Our company's Device Product & Process Development (DPPD) ... products and processes are developed in accordance with applicable regulatory , quality, company, and customer requirements.-This position will lead cross-functional… more
- Merck & Co. (South San Francisco, CA)
- …addressed.Collaborate cross-functionally with medicinal chemistry, pharmacology, clinical, and regulatory teams to advance pipeline programs.Interpret complex data ... guide decision-making.Stay current on emerging science, competitive landscape, and regulatory requirements in respiratory therapeutics.Manage and mentor junior scientists… more
- Merck & Co. (Rahway, NJ)
- …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 & Co. (Rahway, NJ)
- Job DescriptionThe Senior Director (Sr. Principal Scientist) has primary responsibility for the planning and directing clinical research activities involving new or ... including development strategy, study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication.Specifically, the Senior Director May Be… more
- Keurig Dr Pepper (Frisco, TX)
- …needed for this role can be found in the full description below. Sr Principal , Product Owner - Enterprise Data Management Are you ready to redefine how data ... technology and business transformation, this is your moment. Your Mission: As the Sr Principal Product Owner - Enterprise Data Management , you will execute the Data… more
- Usaa (Plano, TX)
- …in a complex institution and/or highly matrixed environment. In-depth knowledge of compliance laws, regulations, and regulatory expectations. Ability to apply ... regulatory risk and compliance knowledge o to consult and provide insights and...description reflects the details considered necessary to describe the principal functions of the job and should not be… more
- USAA (Charlotte, NC)
- …technology, cyber security or related industry. 2 years of experience with relevant regulatory compliance , industry regulations and regulatory data sources ... etc. Proficient knowledge of relevant cyber and/or technology process(es) and regulatory compliance requirements. Strong knowledge of cybersecurity principles… more
- USAA (Charlotte, NC)
- …principles, tools, and applicable systems Awareness and ability to apply risk and compliance laws, regulations, and regulatory expectations. Ability to work with ... We are seeking a motivated and forward-thinking Risk and Compliance Advisor II to join our team and play...description reflects the details considered necessary to describe the principal functions of the job and should not be… more
