- 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
- Tris Pharma (Monmouth Junction, NJ)
- …Operating Procedures (SOPs), current Good Manufacturing Practices (cGMPs) and Food and Drug Administration (FDA) standards. She/he also provides and monitors the ... continuous flow of product and components to all manufacturing areas to ensure adequate supplies are organized and in stock, as needed. ESSENTIAL FUNCTIONS Primary duties/responsibilities Under direct supervision of the Manufacturing Supervisor and/or… 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
- Veterans Health Administration (Wichita, KS)
- …in a testing designated position are subject to urinalysis to screen for illegal drug use prior to appointment. Applicants who refuse to be tested will be denied ... about the Act and the complaint process, visit Human Resources and Administration /Operations, Security, and Preparedness (HRA/OSP) at The Fair Chance Act. Benefits A… 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 (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
- 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
- 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, ... 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 (Los Angeles, 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
- UnitedHealth Group (Springfield, PA)
- …before appointment with the clinician Perform lab services: venipuncture, injection administration , drug screen processing, and specimen collection Receive and ... state, or federal laws, rules, or regulations. OptumCare is a drug -free workplace. Candidates are required to pass a drug test before beginning employment. 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 (Cincinnati, OH)
- …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
- Northwestern University (Chicago, IL)
- …policy & procedure developed by the NU Institutional Review Board (IRB), Food & Drug Administration (FDA) Code of Federal Regulations (CFR), & the International ... scientific papers for presentation & publication & coordinates writing, submission & administration of grants. Ensures that all study activities are completed by… more
- Kestra Medical Technologies, Inc (Memphis, TN)
- …*Kestra manufactures and provides life-saving products regulated by the Federal Food and Drug Administration and under contract with Medicare. Kestra maintains a ... manufactures and provides life-saving products regulated by the Federal Food and Drug Administration and under contract with Medicare. Kestra maintains a drug… more
