Pharmaceutical Jobs in Warren

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..

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 **Business Title:** Manager, Life Sciences, Digital Solutions - Regulatory Affairs, Quality, Safety **Requisition Number:** 63993 - 58 **Function:** Advisory **Area of Interest:** **State:** NJ **City:**..

We are currently looking for a Sr. PD Chemist in our Flanders, New Jersey facility. You will work as a member of the Exterior Coatings Team with a focus on..

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..

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..

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..

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..

View Our Website (http://centershealthcare.com/careers) View All Jobs Thanks for visiting our Job Board. Please review our open positions and apply to the positions that match your qualifications. Medical Laboratory Technologist..

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..

Date: Sep 23, 2021 Location: Parsippany, New Jersey, US, 07054 Company: Teva Pharmaceuticals Company Info Teva is a global pharmaceutical leader and the world's largest generic medicines producer, committed to..

Date: Sep 21, 2021 Location: Parsippany, New Jersey, US, 07054 Company: Teva Pharmaceuticals Company Info Teva is a global pharmaceutical leader and the world's largest generic medicines producer, committed 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..

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..

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..

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..

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..

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..

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..

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..

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..

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..

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..