- Merck & Co. (South San Francisco, CA)
- …optimizing GenAI approaches to streamline the creation and quality control (QC) of regulatory submission documents. The candidate will be part of an ... the assessment of drug candidates. The successful candidate will join a dynamic Data Science team focused on bringing AI/ML approaches to bear to improve the speed… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …diversified, unmet medical needs of people globally by leveraging our world-class science and technology. With more than 125 years of scientific expertise and ... electronic records, validation processes, and regulated applications meet strict regulatory requirements, industry best practices, and internal quality standards.… more
- Legend Biotech USA, Inc. (Baton Rouge, LA)
- …an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking Sr. Medical Science Liaison (South Central) as part of the Medical Affairs team ... in TN, KY, AR, LA, or MS. Role OverviewAs part of the US Medical Affairs team, the Senior...of the US Medical Affairs team, the Senior Medical Science Liaison (MSL) will be responsible for engaging identified… more
- Insmed Incorporated (San Diego, CA)
- …transfers and mentoring junior staff. Maintaining laboratory equipment, ensuring safety and regulatory compliance, and supporting audits are also part of the ... industry, come to Insmed to accelerate your career.RecognitionsConsistently Ranked Science 's Top EmployerInsmed is dedicated to creating a collaborative environment… more
- Formation Bio (New York, NY)
- …drugs than the industry can progress because of the high cost and time of clinical trials. Recognizing that this development bottleneck may ultimately limit the ... values, and every team and individual plays a key part in our mission to bring new treatments to...commercialization. You will oversee internal and external teams, ensure regulatory compliance, and play a key role in scaling… more
- Merck & Co. (North Wales, PA)
- …Drug Development, Ethical Standards, ICH GCP Guidelines, Life Science , Medical Writing, Motivation Management, Ophthalmology, Prioritization, Regulatory ... to demonstrate your leadership, technical skills, and scientific acumen as part of a global, cross functional team.Job ResponsibilitiesResponsible for leading… more
- Genmab (NJ)
- …compassionate, candid, and purposeful, and our business is innovative and rooted in science . We believe that being proudly authentic and determined to be our best ... methodologies that may support innovation and improve efficienciesEngage with regulatory authorities on compound/indication level discussionsActs as a role… more
- Merck & Co. (North Wales, PA)
- …Life Science , Medical Writing, Motivation Management, Prioritization, Project Management, Regulatory Compliance, Regulatory Documents, Science {+ 4 ... have the opportunity to demonstrate your leadership and technical skills as part of a global, cross-functional team. You will apply project management,… more
- Genmab (NJ)
- …experienced Senior Medical Writing Manager to help us tell the story of our science through compelling clinical and regulatory documents. You'll be at the heart ... purposeful, and our business is innovative and rooted in science . We believe that being proudly authentic and determined...a meaningful impact in oncology drug development and be part of a dynamic, collaborative team that values innovation,… more
- Genmab (NJ)
- …compassionate, candid, and purposeful, and our business is innovative and rooted in science . We believe that being proudly authentic and determined to be our best ... methodologies that may support innovation and improve efficienciesEngage with regulatory authorities on compound/indication level discussionsActs as a role… more
- Insmed Incorporated (San Diego, CA)
- …industry, come to Insmed to accelerate your career.RecognitionsConsistently Ranked Science 's Top EmployerInsmed is dedicated to creating a collaborative environment ... where our team can thrive. Every day, our employees turn their passion for science and research into innovative solutions for patients. That's why we've been named… more
- Merck & Co. (Rahway, NJ)
- … Science , Medical Writing, Motivation Management, Prioritization, Problem Solving, Regulatory Compliance, Regulatory Documents {+ 4 more}-Preferred Skills:Job ... demonstrate your leadership, technical skills, and scientific acumen as part of a global, cross-functional team . - Job...clinical scientists. Core Skills Solid knowledge of clinical research regulatory requirements (e . g . , GCP and… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …treatment of multiple myeloma.Legend Biotech is seeking a Global Process Steward as part of the Technical Operations team based in Raritan, NJ. Role OverviewThis ... best-in-class high volume marketed CAR-T product. This effort is business critical and part of a multi-site global manufacturing network whose aim is to maintain… more
- Twist BioScience (South San Francisco, CA)
- …of our proprietary MES technologies will ensure strict adherence to regulatory requirements, optimize complex biological manufacturing processes, and align with our ... continuous improvement, technical excellence, robust software development practices, and regulatory compliance.Software Development & Implementation: Oversee the full Software… more
- Lundbeck (Edmond, OK)
- …SUMMARY: Are you a results-driven biopharmaceutical sales professional looking to be part of an organization that values being curious, adaptable and accountable? ... Environment/Compliance - Ability to apply knowledge of pharmaceutical and regulatory environment, including accountability and adherence to Lundbeck policies and… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …treatment of multiple myeloma.Legend Biotech is seeking a Metrology Technician I/II as part of the Technical Operations team based in Raritan, NJ. Role OverviewThis ... work environment focused on an EHS first mindset, a Right First Time culture of quality, permanent inspection readiness compliance mindset and passionately drives… more
- Formation Bio (New York, NY)
- …drugs than the industry can progress because of the high cost and time of clinical trials. Recognizing that this development bottleneck may ultimately limit the ... values, and every team and individual plays a key part in our mission to bring new treatments to...AI solutions into trial protocols and workflows Partner with regulatory teams to ensure imaging biomarkers and AI models… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Chemical Commercialization Technology (CCT) department, which is part of our Manufacturing Division , is seeking self-motivated individuals who ... effective communication and collaboration skillsGood organizational, interpersonal, writing, and time management skillsLead and operate within a cross-functional process… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …the treatment of multiple myeloma.Legend Biotech is seeking Maintenance Technician I as part of the Technical Operations team based in Raritan, NJ. Role OverviewThis ... thermal energy principals, mechanical maintenance techniques, and electromechanical theoryEnsures regulatory and job training remains current by promptly completing… more
- Genmab (NJ)
- …compassionate, candid, and purposeful, and our business is innovative and rooted in science . We believe that being proudly authentic and determined to be our best ... other analyses not pre-defined in the SAP), answers to questions posed by regulatory authorities or ethics committees, answers to in-house questions related to data… more
