R & D Jobs in Iselin, New Jersey
252 Iselin, NJ R & D jobs found on Monster.
QUALITY SYSTEMS ENGINEER (CQA, Six Sigma, CQE, audits, GMP, FDA) · Perform Quality Engineering Data Analysis for Finished Goods and Raw Material Sampling Plans · Serve as the point person to perform statistical analysis and justifications for process monitoring, protocols and test reports requiring analysis of data · Statistical Process Control for finished goods specifications · Perform DOE (Desi...
Responsibilities · Perform quantitative analysis on routine samples according to established, written procedures (HPLC, dissolution, moisture by KF, GC, TLC, and others to perform pharmaceutical product stability testing.) · Calculate results from experiments and document all laboratory work in accordance with cGMP requirements. · Perform maintenance and calibration activities on laboratory equipm...
Army National Guard
WOODBRIDGE, 07095
As an Army National Guard Chemical Operations Specialist, you'll be there and prepared whenever a community is flooded, an earthquake shakes the foundations of a city, a hurricane makes landfall, or an enemy uses biological or chemical warfare. You will know what to do to evacuate the area, control the situation, and solve the problem. In order to perform these functions, you will be trained to ex...
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 Oncology experience and total of 5+ years of Data Management experience · Require MediData Rave or Inform experience. · e/CRF Design – Review and approve CRF design, data review ground rules and databa...
Sr. Clinical SAS Programmer - Onsite or Remote. Positions are based in NJ, NC, TX and CA locations. For additional information please email me your resume at - arati.kapileshwari@maxisit.com Senior computer programming position working with clinical trials data. Primary responsibilities include providing clinical data management and biostatistical programming support for various phases of clinical...
Job Title: Administrative Project Coordinator - Clinical data entry (Full time Perm position – Must be Onsite) Please email your resume to arati.kapileshwari@maxisit.com Job Description: · Develops and maintains a detailed project schedule which includes administrative tasks and all sites involved in the project. · Participation in Team Meetings and Coordinate meetings · Maintain Project Managers...
PerkinElmer is a global technology leader driving growth and initiative in the Environmental and Human Health Science markets. The company is a leading force in the development, production, marketing, servicing, and support of laboratory instrumentation and ancillary services throughout the world. Relocation – Associate CSE Function: Service Location: Field Reports to: Regional Business Manager/Pr...
PerkinElmer is a global technology leader driving growth and initiative in the Environmental and Human Health Science markets. The company is a leading force in the development, production, marketing, servicing, and support of laboratory instrumentation and ancillary services throughout the world. Project Manager (Relocations) To lead, manage and provide planning and execution direction in multipl...
Company Confidential
Edison, NJ
Our client is a biopharmaceutical company focused on the discovery, development and commercialization of small-molecule drugs. They have collaborations with leading pharmaceutical and biotechnology companies such as Pfizer, Celgene, and Schering Plough (Merck). This position contributes to the drug discovery and drug product development process by developing formulations for preclinical and clinic...
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 take ownership of their research to a...
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...
Champion aspects of transgenic and knockout production at a major company including embryo production and recovery in transgenic and knockout mice by performing: * Pronuclear and blastocyst injections * Egg and blastocyst implantation into pseudo pregnant mice * Hormone injection to induce super-ovulation * Identify pseudo-pregnant recipients for embryo transfers * Collect mouse eggs and blastocys...
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...
License/Certification/Education: Normally B.A./B.S. in Science w/1-2 years of experience. Job Description: Conducts audits for the regulatory/QA function within the Clinical Trials Department in order to help assure compliance with GLP/GCP in accordance with established FDA regulations and company policies and standard operating procedures. Reviews data and reports emanating from laboratory Clinic...
The Formulation Development Technician II would assist the Formulators and Engineers in new product development. The Technician II would clean, set-up and operate equipments used in development and exhibit batches. Able to perform data entry into computer and batch calculations with minimum supervision. The Technician II will be responsible for manufacture of products as per the batch records. Mai...
Basic Purpose: This position is responsible for independently creating and implementing formulation development strategies. Formulation leader within team based structure and provides direction for the progress of team projects. The person functions as a subject matter expert in dealing with government agencies and external contract research organizations. Co-ordinates with other departments to ge...
. Develops complex methods, optimizes methods, and troubleshoots and validates analytical methods used in the Quality Control Laboratory. Investigates test failures. Analyzes and interprets results in written and/or oral format. Essential Functions and Responsibilities: · Develops and optimizes complex methods for in-process, process validation, raw materials, finished products, stability and deve...
Company Confidential
Berkeley Heights, NJ, 07922
We have several positions and are eagerly reviewing new candidates. Please submit your resume if you feel you meet the necessary requirements below: The Clinical Trials Associate (CTA) is involved in the conduct of the study and interfaces with the Study Manager and the Study Team. Requirements: BA/BS in directly-relevant discipline or equivalent experience required At least 2 years experience as...
Part Time Field Staff Needed On behalf of Research Triangle Institute, Headway Workforce Solutions is seeking part time Field Staff to work on a government sponsored research study in New Brunswick, NJ. Candidates must live close to the coast. POSITION SUMMARY RTI International is seeking to hire field interviewers for the Access-Point Angler Intercept Survey. This important research study, sponso...
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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: 2013.5.0.223-326 
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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: 2013.5.0.223-326