New Brunswick
R & D Jobs in New Brunswick, New Jersey
162 New Brunswick, NJ R & D jobs found on Monster.
Hello, Please do let me know if you are available for the below position. Job Title: Labware LIMS Developer Location: New Brunswick, NJ Duration: Long Term Job description: Must have significant experience and demonstrated proficiency in the support, maintenance and use of large or complex systems. LabWare LIMS v6 (and v5) experience highly desirable. Experience with laboratory instrument systems,...
Seeking extensive clinical development experience to help guide discovery strategies and focus pre-clinical resources and efforts most effectively for big pharma research & development activities. Must be a strategic expert and savvy diplomat to work closely with global pharma CEO in the analysis, selection and internal promotion of drug development strategies from evidence-based medicine to susta...
Establish and manage and an effective and knowledgeable quality and compliance organization, with specialization in providing quality oversight for commissioning, qualification, and validation of GMP facilities, utilities, equipment, instruments and computer systems used in the manufacture of clinical supplies. Additionally, lead and manage computerized systems compliance audits for applications a...
Position: Validation Specialist I Location: New Brunswick, NJ Job Description and Responsibilities: • Manage routine calibration, validation documentation and monitoring systems. • Generate and execute all Validation protocols (IQ/OQ/PQ) of all site equipment including production equipment, product storage, utilities (as applicable) and other related systems in an FDA regulated environment. • Asse...
Level dependent upon experience/qualifications. Under the general direction of a more senior staff or director, the incumbent is primarily responsible for designing and preparing novel animal health formulations. As a senior staff member, the incumbent is responsible for conducting, planning, and prioritizing complex research and development activities and representing the department on multidisci...
Under a general direction of a more senior staff or director, the incumbent will be primarily responsible for developing analytical methods for bulk drugs and finished dosage forms. The individual is expected to work under GLP/GMPs and serve as a Study Director on GLP studies. Major responsibilities include the following: Reporting to a more senior staff member/director from whom assignments are r...
Global pharmaceutical company is seeking a Director of Quality. In this critical role, you will head all quality operations for GMP manufacturing. We are looking for a forward thinking quality professional to maintain and build upon our “quality first” approach to providing pharmaceuticals. The Director of Quality is responsible for the site’s quality systems ensuring the connection with manufactu...
New Brunswick, NJ Pharmaceutical DEA Data Reviewer Our client is seeking a full-time DEA Data Reviewer to join their growing pharmaceutical organization. Great opportunity with excellent benefits and compensation! Summary: The DEA Data Reviewer is responsible for DEA reporting and Documentation, review of data for DEA review, and trending/tracking errors to provide resolution to correct documentat...
To independently perform and direct in vivo and in vitro drug metabolism as well as tissue residue studies within Drug Safety and Disposition to support Merial drug development for both production and companion animal products. The incumbent will develop and validate methods, including methods to identify and profile metabolites, with little or no guidance, and provide guidance to others in suppor...
This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. Our Senior SAS Programmer Analysts play a key role within ICON developing and executing execute statistical programs designed to analyze clinical trial information. The Senior SAS Programme...
Job_Other_Compensation: We have an immediate need for a Chemist ESSENTIAL DUTIES AND RESPONSIBILITIES: Ability to perform all test procedures and handle instrumentation/equipment used in testing which includes Gas Chromatographs, UV-Visible Spectrometers, titrators, Melt Flow Indexer, various particle size determination techniques and classical lab apparatuses. Perform polymerizations and physical...
ITC is a world leader in the development and manufacturing of Point-of Care blood coagulation and clinical diagnostic systems. We are committed to developing, manufacturing & marketing safe, easy to use, & reliable products that are used by doctors, nurses & medical practitioners where care is provided to patients. We currently have an opening in for a R&D Engineering Managerin our Piscataway loca...
Sample Accountability - Coordinators & Analyst 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 Sample Accountability Department. With over 25 years of conti...
Job Qualifications: Good Experience in SDTM and ADAM At least 4 years of professional experience in Creating SDTM mapping specifications, Developing and Validating SDTM standard and non-standard domains At least 1 year of team leading experience of CDISC team Familiar with CDISC compliance checking At least 4 years of professional experience in SAS programming Job Requirement: Bachelor Degree or M...
Croda Inc is a world-class leading supplier of high quality, innovative specialty ingredients used in the personal care, pharmaceutical, household, and industrial markets. The culture of Croda Inc is one that values and respects the individual and their contribution to the Company’s results. Our aim is to provide a safe work environment where employees are encouraged to communicate with management...
Requirements: Bachelor's degree Experienced CRA with 5+ years of recent direct monitoring Must have strong inpatient hospital chart/EMR experience 3 plus years of Oncology monitoring required Inpatient monitoring experience Travel is expected to be, on average, 75%, sometimes more depending on trial demands. Must have home office Phase II-III trial experience...
Lead Clinical Data Manager – Full Time Permanent position in Metuchen, NJ All work to be performed onsite. For additional details please email me your resume at – arati.kapileshwari@maxisit.com Must have 3 yrs of Oncology experience and total of 6-7 years of Data Management experience · Require MediData Rave experience. · e/CRF Design – Review and approve CRF design, data review ground rules and d...
GENEWIZ, Inc. is an award-winning global contract research organization (CRO) specializing in DNA services. Excelling in both science and customer support, GENEWIZ is a trusted provider for DNA sequencing, gene synthesis, molecular biology, genomic, next generation sequencing, bioinformatics, and GxP/CLIA regulatory services. Customers depend on GENEWIZ to achieve results in a rapid, cost-effe...
Education: Associates or BA/BS Experience: Regulatory in Pharma or CRO Summary: Provides submission compilation, filing and archiving expertise in the acquisition, quality control, retention, and submission of nonclinical, CMC, and clinical regulatory documents and other sponsor-specific essential documents. Maintains electronic and hardcopy files, assures completeness of the records, and helps en...
GENEWIZ, Inc. is an award-winning global contract research organization (CRO) specializing in DNA services. Excelling in both science and customer support, GENEWIZ is a trusted provider for DNA sequencing, gene synthesis, molecular biology, genomic, next generation sequencing, bioinformatics, and GxP/CLIA regulatory services. Customers depend on GENEWIZ to achieve results in a rapid, cost-effe...
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If three resistances, 6 ohms, 12 ohms,and 18 ohms, are connected in series across 36 volts,...?
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©2013 Monster - All Rights Reserved U.S. Patents No. 5,832,497; 7,599,930 B1; 7,827,125 and 7,836,060 MWW - Looking for Monster Cable? - V: 2013.1.5.22-211 
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©2013 Monster - All Rights Reserved U.S. Patents No. 5,832,497; 7,599,930 B1; 7,827,125 and 7,836,060 MWW - Looking for Monster Cable? - V: 2013.1.5.22-211