R & D Jobs in New Jersey

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821 New Jersey R & D jobs found on Monster.

Jobs 1 to 20 of 821
Manager Medical Affairs Location: Jersey City NJ Duration: 5 months Requirements: -PharmD, Ph.D, or MD preferred -The position is for Infectious Disease therapy area promotional material (Promotional Review Committee [PRC]) review as per pharmaceutical industry guidelines -Must have PRC experience (4 years) -Infectious disease therapeutic areas expertise highly valued -Medical Affairs expe...
ESSENTIAL DUTIES AND RESPONSIBILITIES: Develops multiple processes in the laboratory, scaling up and overseeing the processes, according to cGMP guidelines and ISO 17025 requirements. Well versed in all USP microbiological testing, especially USP , , . Maintains laboratory policy and procedure manuals and assists in developing and writing procedures; validates the procedures and document prepar...
Organic Extractions Supervisor Accutest Laboratories is a nationwide environmental testing laboratory that has successfully delivered defensible data for over 50 years. Founded in 1956, Accutest is the nation's 3rd largest environmental testing laboratory combining advanced technology and experienced personnel to deliver "Total Performance You Can Count On". Accutest Laboratories in Dayton, NJ i...
One of the world’s leading chemical companies has a job opening in their central New Jersey location. The company seeks a research engineer with a degree in Chemistry or Chemical Engineering to work on experimentation related to catalysts that reduce harmful emission gases. The company designs and develops catalysts and adsorbents used to treat and purify emission gases from power plants, or from...
inVentiv Health – Transforming Promising Ideas into Commercial Reality Job Title: Sr. Clinical QA Auditor Job Description: · Conduct and/or assist with the conduct of audits of the Company’s projects, processes, systems and vendors as assigned and in accordance with the Annual Audit Plan with minimal supervision · Facilitate or assist with facilitation of client audits and regulatory inspectio...
Theradex® is an international contract research organization with over 30 years of experience providing complete professional services for the clinical research and development of pharmaceutical compounds, medical devices and diagnostic tests in the areas of oncology and life-threatening diseases. Theradex® conducts clinical trials towards the goal of marketing approval for new agents with the pot...
Title: Manager Medical Affairs. The position is for Infectious Disease therapy area promotional material (Promotional Review Committee [PRC]) review as per pharmaceutical industry guidelines Education: PharmD, Ph.D, or MD preferred. Experience: Must have PRC experience (4 years), infectious disease therapeutic areas expertise highly valued, and Medical Affairs experience (4 years) in Pharmaceut...
Theradex® is an international contract research organization with over 30 years of experience providing complete professional services for the clinical research and development of pharmaceutical compounds, medical devices and diagnostic tests in the areas of oncology and life-threatening diseases. Theradex® conducts clinical trials towards the goal of marketing approval for new agents with the pot...
BIOLOGICAL RESEARCH SCIENTIST WITH ASSAY DESIGN EXPERIENCE REQUIREMENT #14-01171 RECRUITER: MELISSA GIUSTI JOB LOCATION: HOPEWELL, NJ OCTOBER 24, 2014 Project Description: Basic knowledge of the drug discovery process and independence in experimental / assay design, data analysis and problem solving Working knowledge and experience with a wide range of technical skills relevant to the speci...
Xenobiotic Laboratories (XBL), a subsidiary of the Lab Testing Division of WuXi AppTec, Inc., is a leading contract research laboratory specializing in small molecule bioanalytical, drug metabolism, and pharmacokinetic services to the pharmaceutical, animal health and agrochemical industries. XBL is seeking an experienced autoradiography research professional to lead the QWBA group to conduct stud...
J. Knipper and Company’s continued growth as the Pharmaceutical industry’s leading sample services provider, creates long term career opportunities for high performing individuals with a strong desire to learn, succeed, and advance. One of those opportunities is now available in our premier Professional Services Department. With over 25 years of continued growth as one of the largest employers in...
Job Number: 424074 SAS Programmer II OVERVIEW Provide statistical programming expertise in SAS for the production of analyses, tabulations, graphics, and listings from clinical trial data. Key responsibilities and skills include, but are not limited to, the following: Contribute to the preparation of analysis plans. Prepare, document and test required programs and procedure data displays in ...
Auditor Principal Specialist GCP Requirements: - Bachelor degree preferably in a life / medical / natural sciences or scientific discipline - 10 to 14 years of pharmaceutical (or related) experience with BA or 8 to 12 years with advanced degree, e.g. MBA, MS, PharmD, PhD. This includes a minimum of 6 years of Clinical Quality Assurance related experience and/or experience in Clinical Trials suc...
Clinical Pharmacologist/Toxicologist Beta Pharma, Inc is seeking a driven Clinical Pharmacologist/Toxicologistto manage all nonclinical and preclinical affairs, including clinical pharmacology and toxicology development strategy, design and management of nonclinical and preclinical studies. The successful candidate will additionally manage CRO selection and oversee timelines and budgets. Beta Ph...
Ortho-Clinical Diagnostics, Inc. (OCD) is a leading provider of in vitro diagnostic products and services, offering accurate, timely, and cost-effective solutions for screening, diagnosing, monitoring and confirming diseases. The company has approximately 3,800 employees around the world serving the global clinical laboratory and transfusion medicine community, and is committed to providing custom...
Product Complaint Associate JOB SUMMARY: The Product Complaints Associate will manage the administration of the Clinical and Commercial Complaints systems including the receipt, coordination of returns, investigation and final correspondence of all Product Complaints for Global Products. This role will drive the Investigation process for QA with emphasis on compliance to SOPs and applicable Regu...
Ortho-Clinical Diagnostics is recruiting for a Corporate Account Manager-Distribution in our Commercial Sales Department and will be Field Based. Ortho Clinical Diagnostics (OCD) is a leading provider of in vitro diagnostic products and services, offering accurate, timely, and cost-effective solutions for screening, diagnosing, monitoring and confirming diseases. The company has approximately 3,8...
Ortho-Clinical Diagnostics is recruiting for an IDN National Account Manager in our Commercial Sales Department and will be work from home, covering nationally. Ortho Clinical Diagnostics (OCD) is a leading provider of in vitro diagnostic products and services, offering accurate, timely, and cost-effective solutions for screening, diagnosing, monitoring and confirming diseases. The company has ap...
Regulatory Documentation Coordinator You're precision-oriented and a stickler for doing it right. You have deep expertise in pharmaceutical compliance and quality control. Your critical thinking prowess makes you a problem solver extraordinaire. You generate powerful ideas and know how to get them implemented. If this describes you, this opportunity from Experis is just right for you. ***This is...
Ortho-Clinical Diagnostics, Inc. (OCD) is a leading provider ofin vitrodiagnostic products and services, offering accurate, timely, and cost-effective solutions for screening, diagnosing, monitoring and confirming diseases. The company has approximately 3,800 employees around the world serving the global clinical laboratory and transfusion medicine community, and is committed to providing customer...

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