- Eisai, Inc (Nutley, NJ)
- …Director will direct the development and submission of investigational drug applications, product registration dossiers, supplements, amendments, as well as ... of 10 years direct Regulatory Affairs experience in the biotech/biopharmaceutical industry. Education area of study in a scientific discipline with a Master's or… more
- Merck & Co. (Rahway, NJ)
- …several factors including, but not limited to relevant education , qualifications, certifications, experience, skills, geographic location, government requirements, ... Testing, Clinical Trial Management, Cross-Cultural Awareness, Cross-Functional Teamwork, Dermatology, Drug Development, Ethical Compliance, Ethical Standards, Immunoassays, Immunotherapy, Management… more
- Aequor (Davie, FL)
- …Rate: /hr Pay rate: /hr mins interview Screening Requirements: Basic Background 12-Panel Drug Test - yes Medical Screenings: A) Vision Screen - Near, Far, Color, ... accepted practice is required. POSITION REQUIREMENTS Any equivalent combination of education , training and/or experience that fulfills the requirements of the… more
- Eisai, Inc (Seattle, WA)
- …regulations impacting the pharmaceutical industry (eg, PhRMA Code; Federal Food, Drug , Cosmetic Act; Anti-Kickback Statute; False Claims Act, OIG/DOJ Guidance; ... depend on various factors including but not limited to experience level, education , knowledge, and skills.Employees are eligible to participate in Company employee… more
- BioAgilytix (Durham, NC)
- …fast-paced, fun and never boring. Because we work across numerous clients and drug modalities, your career can develop rapidly. You'll gain experience with a variety ... GxP guidelines)Additional Responsibilities:Other duties as neededMinimum Preferred Qualifications - Education /Experience:Bachelor's degree in molecular biology, biochemistry, immunology, biotechnology, or… more
- Merck & Co. (Durham, NC)
- …our Intermediate Adjuvant manufacturing process and Sterile Supply manufacturing for Bulk Drug Substance. Focused areas of responsibility include but are not limited ... to develop reliable, consistent manufacturing processes that meet cGMP requirements. Education Minimum Requirement:-High School Diploma/GED or higherMinimum Required Experience… more
- Merck & Co. (Rahway, NJ)
- …establish a consolidated, visible forecast for all study product needs (Bulk Drug Product and Clinical Finished Goods).-- Responsible for authoring clinical supply ... work location and the chosen candidate's relevant skills, experience, and education . Expected US salary range: $114,700.00 - $180,500.00Available benefits include… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …investigational sites. Additionally, this position possesses adequate knowledge of drug development in pharmaceutical industry across different disease areas, and ... to meet the qualifications below with or without a reasonable accommodation. Education Qualifications (from an accredited college or university)- Master's degree in… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …to meet the qualifications below with or without a reasonable accommodation. Education Qualifications (from an accredited college or university)- Master's Degree ... reporting of clinical trials. preferred- Having knowledge of all phases of drug development, including early and late phase clinical development and submission… more
- BioAgilytix (Durham, NC)
- …fast-paced, fun and never boring. Because we work across numerous clients and drug modalities, your career can develop rapidly. You'll gain experience with a variety ... LIMS systemAdditional ResponsibilitiesOther duties as neededMinimum Preferred Qualifications - Education /ExperienceBachelor's degree in molecular biology, biology, biochemistry, immunology, biotechnology,… more
