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At Bristol Myers Squibb we are inspired by a single vision transforming patients lives through science In oncology hematology immunology and cardiovascular disease and one of the most diverse and..
n nJob Description nJoin a Legacy of Innovation 110 Years and Counting Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of..
About AbbVieAbbVie’s mission is to discover and deliver innovative medicines that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact..
Job Title : Clinical Project Manager - Pharmaceutical Duration : 12 Months Job Description: Collaboratively and proactively supports and offers Project Management leadership within a cross-functional team within WW Oncology..
At Bristol Myers Squibb, we are inspired by a single vision – transforming patients’ lives through science. In oncology, hematology, immunology and cardiovascular disease – and one of the most..
Job DescriptionnnWe are a research-driven biopharmaceutical company. Our mission is built on the simple premise that if we u201cfollow the scienceu201d that great medicines can make a significant impact to..
Job DescriptionnnSubject to applicable law, all prospective hires will be required to demonstrate that they have been fully vaccinated for COVID-19 or intend to be vaccinated for COVID-19 by November..
Job DescriptionnnSubject to applicable law,u00a0 all prospective hires will be required to demonstrate that they have been fully vaccinated for COVID-19 or intend to be vaccinated for COVID-19 by November..
Regulatory Affairs Specialist Role with a World-Class Medical Device Company!! Regulatory Affairs Specialist Duties and Responsibilities: Support new product development and commercial programs by interacting with cross-functional project teams in..
OverviewnKashiv BioSciences is a fully integrated biosciences company with an expanded and dynamic platform for growth including advanced drug delivery technologies, biosimilars, prodrugs, and a large development pipeline. We are..
Job Title : Compliance Specialist Duration : 06 Months Job Description • Manage and coordinate activities associated with the GxP IT Quality Assurance (QA) program for GPS and R&D computerized..
Overview Do you have a noticeable passion for results?You're bold, empathetic, and very resourceful, especially when results are at stake. You have what it takes: a competitive drive coupled with..
The Associate Director of Clinical Drug Supply & Logistics (CDSL) - Operations is responsible for driving the strategy, optimization and execution of business processes and analytic capabilities for the CDSL..
Job DescriptionnnPrincipal Scientist (R5) u2013 Biologics AR&D u2013 Analytical Method DevelopmentnOur Research Scientists are our Inventors. We identify and target steps in disease mechanisms or pathways that could be inhibited..
The Associate Director, Therapeutic Area Project Management (TAPM) provides project management leadership for the cross functional clinical development teams, ensuring targets are met on time and with quality. We are..
Apply on the Company Site Are you an experienced clinical laboratory professional looking for leadership opportunity? Are you detail oriented, process focused, and enjoy leading others? Are you looking for..
Apply on the Company Site **Business Title:** Manager, Life Sciences, Digital Solutions - Regulatory Affairs, Quality, Safety **Requisition Number:** 63993 - 58 **Function:** Advisory **Area of Interest:** **State:** NJ **City:**..
Title: Product Complaint Specialist nLocation: New Brunswick, NJ nStart date: ASAP nResponsibilities: n n Perform accurate review, evaluation and assignment of incoming product quality complaints within established timeframes n Assess..
Job DescriptionnnThe Quantitative Pharmacology and Pharmacometrics (QP2) department within Pharmacokinetics, Pharmacodynamics, and Drug Metabolism (PPDM) drives model-informed drug discovery and development (MIDD) to routinely enable efficient drug discovery/development and/or regulatory..