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Supports all functions, goals, and objectives of the department as well as development of any new programs that involve the Neurodiagnostic Lab and Epilepsy Unit. Performs all the duties of the Neurodiagnostic Technologist Level 1.
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The CMC Regulatory Technical Writer II authors high quality Module 2 and 3 regulatory submissions for both development and post-approval dossiers, change controls and technical reports. The CMC Regulatory Technical Writer II authors high quality Module 2 and 3 regulatory submissions for both development and post-approval dossiers, change controls and technical reports.
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We're seeking a vigilant and dedicated professional to fill the position of Pharmacovigilance Case Management Head. If you have a keen eye for detail, a passion for pharmacovigilance regulations, and a commitment to maintaining the highest standards of drug safety, we invite you to apply.
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Talent development is a managerial principle at Kering and we are committed to fostering internal mobility. This is a fabulous opportunity to join the Kering Eyewear adventure and to actively contribute to the development of the business by becoming part of a thriving Company in a global Luxury Group that offers endless possibilities to learn and grow.
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Demonstrated hands-on product development experience and knowledge in Dairy & Dairy Alternative Category Application segment (Yogurt & Fermented Milk products, Cheese, Ice Cream, Frozen Desserts, Ready-to-Drink Beverages, and their Plant-Based Alternatives)Knowledge of ingredient selection and differentiation related to selecting and formulating with Starches, Hydrocolloids, Proteins, Specialty Sweeteners, Flavors, Enzymes, and Cultures regarding Dairy and Dairy Alternative applications.
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Solid understanding of medical concepts and familiarity with safety activities in drug development and post marketing and global safety health authority requirements. The Associate Director (AD) Safety Analysis Scientist (SAS) provides scientific expertise and leads the safety assessment of assigned assets for Johnson & Johnson Enterprise Innovation.
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Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market.
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Hands-on experience in nucleic acid drug formulation and development (especially nanoparticle delivery technologies) is required. BS degree plus minimum 6 years or Master degree plus minimum 4 years of experience OR PhD plus 1 year of experience in Pharmaceutics, Chemistry, Biomedical Engineering, Chemical Engineering, or related field with a strong background in nanoparticle-based formulation development & analytical characterization.
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Benefits: Bonus based on performance Opportunity for advancement Training & development The Exercise Coach®- Montgomery, NJ: Health Coach / Personal Trainer – Part time If you can, without hesitation, say YES to the statements below, let’s connect.
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Skills: FDA, Food Product Development, USDA. Support planning (will include ordering/requesting ingredients), execute and manage concept and development trials for medical nutrition and consumer care products as well as VMS products according to project scope/brief.
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Leads strategic consultation, and guidance to the PV scientists on decisions that have significant drug safety implications, including safety signal detection activities of monitoring, evaluation, interpretation and appropriate management and communication of safety information for Insmed’s portfolio of products in development.
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Through economic development and community empowerment, we elevate the Navajo Nation to provide lasting impact and sustainable growth for future generations. Diné Development Corporation (DDC) is a Navajo Nation owned family of companies that delivers IT, professional, and environmental solutions to advance the missions of federal, state, and tribal government agencies.
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Located in Dublin, Cruiserath Biologics Campus, a one billion Multi-Product Cell Culture Biologics Manufacturing facility plays a central role in the Global Product Development and Supply (GPS) network as the company's first European biologics manufacturing facility.
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Familiarity/experience with end-to-end CMC drug development. Knowledge and Understanding of Drug Development Processes. The Technical Project Manager will be a key member of the Cell Therapy Development (CTD) Development Operations & Services (DO&S) Portfolio Management Office.
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QualificationsWhat we are looking forRequired Qualifications A minimum of a bachelor’s degree5+ years of Consumer Products industry experience in Category or Customer Strategy, Customer Business Development, Category Insights & Analytics, and/or Shopper Insights & analytics Extensive knowledge of omni-retail customer store operations, structure, strategy, and retail execution tactics.
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drug development jobs Title: director safety in Somerset, NJ
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