- Tris Pharma (Monmouth Junction, NJ)
- …GC, GC-MS, ICP-MS, TLC and dissolution apparatusWorking knowledge of cGMP, Food and Drug Administration (FDA), Drug Enforcement Administration (DEA) ... and Occupational Safety and Health Administration (OSHA) regulations and guidancesThorough knowledge of MV parameters and relevance in method performance and method life cycle managementStrong technical writing skills, including SOPs, investigations,… more
- Tris Pharma (Monmouth Junction, NJ)
- …HPLC, UV/Vis, GC, TLC and dissolution apparatusWorking knowledge of cGMP, Food and Drug Administration (FDA), Drug Enforcement Administration (DEA) ... and Occupational Safety and Health Administration (OSHA) regulations and guidancesAbility to perform analytical testing, calculations and data analysis, as instructedAbility to perform wet chemistry and physical testings, as instructedProficiency with… more
- Tris Pharma (Monmouth Junction, NJ)
- …procedures throughout the organization. Ensures compliance with all current GxPs, Food and Drug Administration (FDA), Drug Enforcement Administration ... (DEA), and Occupational Health and Safety Administration (OSHA) regulations, as well as all applicable company compliance guidelines, standards and objectives Leads and/or oversees functions (ie, purchasing/procurement, warehousing, logistics, etc.) to… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …local, state and federal regulations including and equivalent to Federal Drug Administration (FDA), Environmental Protection Agency (EPA), Occupational Safety ... and Health Administration (OSHA), and Drug Enforcement Agency (DEA) as applicable (TSA) Transportation Security AdministrationAbility to work hours from… more
- Merck & Co. (Rahway, NJ)
- …& Technology (DD&T) organization designs, develops, and commercializes novel biologic/ drug / vaccine - device enabled combination products to achieve safe and ... products across a variety of therapy areas and routes of administration including inhalation, implantation, and injection.--This position serves as a senior… more
- Merck & Co. (Rahway, NJ)
- …In summary, our team enables the translation of preclinical candidates into non-oral drug products.We are seeking a highly motivated candidate for the position of ... Principal Scientist (R5) focused on developing parenteral drug products across a range of modalities (small molecule, peptides, proteins, antibody- drug … more
- Merck & Co. (Rahway, NJ)
- …team is responsible for the research and development of sterile & parenteral drug products for biologics, Antibody Drug Conjugates and Small Molecules, including ... include those administered via intravenous, subcutaneous, or intramuscular routes of administration . This research opportunity is fast paced and contributes to the… more
- Merck & Co. (Rahway, NJ)
- …Development & Technology (DD&T) Team designs, develops, and commercializes novel biologic/ drug /vaccine - device enabled combination products to achieve safe and ... products across a variety of therapy areas and routes of administration including inhalation, implantation, and injection.-- Job descriptionThis position will be… more
- Merck & Co. (Rahway, NJ)
- …vendor support.-Provide facility engineering support and capital project administration (processing capital requests and administering capital project closeout ... engineering or science plus a minimum of 3 years of related Drug Product/sterile experience. Required Experience and Skills :-Strong familiarity with Quality, cGMP,… more
- Eisai, Inc (Phoenix, AZ)
- …and safety messaging and information about product access / safe administration to relevant customer stakeholders in a compliant way.Monitor operating costs ... regulations impacting the pharmaceutical industry (eg, PhRMA Code; Federal Food, Drug , Cosmetic Act; Anti-Kickback Statute; False Claims Act, OIG/DOJ Guidance;… more
- Merck & Co. (Rahway, NJ)
- …development, and supplying Active Pharmaceutical Ingredient (API) for clinical use and drug product development. This will involve handling of a variety of reagents, ... processes, moving from the laboratory to the pilot scale.Familiarity with the administration of cGMPs, Good Documentation Practices (GDPs), and S&E regulations as it… more
- Eisai, Inc (Nutley, NJ)
- …guidelines.Direct program level oversight of Clinical development plans (CDP) and drug development Plans (DDP) for marketed products as well developmental compounds ... and requests for study related information.Strong knowledge base of the drug development process.Deep knowledge of the specific therapeutic area.Proven track record… more
- Eisai, Inc (Indianapolis, IN)
- …regulations impacting the pharmaceutical industry (eg, PhRMA Code; Federal Food, Drug , Cosmetic Act; Anti-Kickback Statute; False Claims Act, OIG/DOJ Guidance; ... Department of Homeland Security in partnership with the Social Security Administration that allows participating employers to electronically verify the employment… more
- Eisai, Inc (Exton, PA)
- …focused on the technology transfer, scale-up, and optimization of validatable biological Drug Substance (DS) / Antibody Drug Intermediate (ADI) production ... Department of Homeland Security in partnership with the Social Security Administration that allows participating employers to electronically verify the employment… more
- Eisai, Inc (Modesto, CA)
- …knowledge. Presentation skills, teaching skills, and confidence in discussing drug information/ disease state management. Prior experience in clinical research, ... drug development and/or clinical pharmacy and a basic understanding...of Homeland Security in partnership with the Social Security Administration that allows participating employers to electronically verify the… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …Execution Systems Lead and will be responsible for EBR development and administration at the Raritan site to support production processing while liaising with ... salary or other discretionary compensation at any time based on individual, team, performance, or market conditions.Legend Biotech maintains a drug -free workplace. more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …documentation for qualified equipment/systems (audit trails, user groups, system administration )Provide expertise and solutions to issues regarding qualification and ... salary or other discretionary compensation at any time based on individual, team, performance, or market conditions.Legend Biotech maintains a drug -free workplace. more
- Eisai, Inc (Nutley, NJ)
- …therapeutic area(s); comfortable and confident speaking about multiple drug indications/disease state management and competitor products and data.Understanding ... Department of Homeland Security in partnership with the Social Security Administration that allows participating employers to electronically verify the employment… more
- Eisai, Inc (Minneapolis, MN)
- …broad-based scientific and pharmaceutical knowledge.Clinical trial development and drug launch experience is strongly preferred.Knowledge of treatment guidelines, ... Department of Homeland Security in partnership with the Social Security Administration that allows participating employers to electronically verify the employment… more
- Eisai, Inc (Nutley, NJ)
- …Director will direct the development and submission of investigational drug applications, product registration dossiers, supplements, amendments, as well as ... Department of Homeland Security in partnership with the Social Security Administration that allows participating employers to electronically verify the employment… more
