R & D Jobs in Atlantic City, New Jersey

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Ocean County based manufacturing company has a need for multiple cleanroom technicians to aid in their manufacturing process. This is a contract position with an opportunity to convert to a permanent position. There are 1st and 2nd shift openings available for qualified candidates. Qualified candidates MUST have: - HS Diploma. - Previous experience working in a cleanroom under GMP guidelines. ...
Position Details: Position: Research Scientist Location: Pennington , New Jersey 08534 Duration: 3+Months Contract (40 hrs/week) Job 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 specific biology field. · E...
Job duties include but are not limited to: * Participate in FDA and Client Audits. * Review Chemist's EXCEL Data Spreadsheets & Lab Notebooks. * Verify Instrument Calibrations from daily Internal Testing and periodic 3rd Party Service Testing. * Be a "working" Manager and doing Methods Development and/or BenchAssays, as needed. * Have good people Skills to work with existing Staff and essenti...
W-2 ONLY ... CONTRACT / 12-14 MONTHS ... GREAT OPPORTUNITY ... CDISC Version 2.3, SAS, SQL, ANALYTICAL DATABASE DESIGN A MUST Duties 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 p...
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...
Growing Pharmaceutical client in Central/Northern NJ area is looking to fill a temp-to-perm role for a Director, Quality Assurance/Auditing with large molecule, biologic experience. This job will have the following responsibilities: ·Manufacturing is done on-site, so client needs a hands-on leader to oversee QA and internal audit compliance. ·Primarily GMP, but some GLP and GCP oversight as wel...
This a terrific opportunity for an Investigation Associate with a niche generic pharmaceutical company engaged in the manufacturing of multi-source and branded pharmaceuticals for pain management and anesthesia in the United States and across the globe. This ever growing company is looking for an Investigation Associate to come on board to their NJ facility. SUMMARY: Reviews, coordinates, and as...
Please note this is a 2+ months contract position Skills: Consumer Chemist, GMP/Lab experience, Validation Products Detailed Job Description: Provide technical support to TT staff in formulated products. This includes Technology transfer, lab, pre-pilot, trial and validation for new products. Provide technical assessment of TT Consumer projects against the Product/process specification. When...
GENEWIZ, Inc. is a leading global genomics service company. Excelling in both science and customer support, GENEWIZ is a trusted provider for DNA sequencing, gene synthesis, molecular biology, next generation sequencing, bioinformatics, and GLP regulatory services. Customers depend on GENEWIZ to achieve results in a rapid, cost-effective manner through specialized expertise and customizable, scala...
Johnson & Johnson companies are equal opportunity employers. Associate Director, Regulatory Program Management-5590140917 Description Janssen Research and Development, LLC, a member of Johnson & Johnson's Family of Companies, is recruiting for an Associate Director, Regulatory Program Management to be located in Raritan, NJ; Titusville, NJ; or Spring House, PA. Janssen Research & Development, ...
XenoBiotic Laboratories, Inc. (XBL), a GLP-regulated Pharmaceutical Development Contract Research Organization located in central NJ. Primary Duties and Responsibilities: · Under regular close supervision, individual performs routine laboratory techniques. · Receives specific instructions on assigned task and expected results. · Maintains research notebooks in a well-organized manner. All nece...
Responsibilities: XenoBiotic Laboratories, Inc. (XBL), a GLP-regulated Pharmaceutical Development Contract Research Organization located in central NJ, is seeking an experienced autoradiography research professional to lead the QWBA group to conduct studies as well as manage and participate in other preclinical ADME studies. The successful candidate will serve as a Study Director/Group Leader in...
2 openings follow AVP of Marketing reports to VP of Marketing. VP of Marketing reports to VP/Head of Commercial Strategy & Operations. AVP will manage 5 groups with 5 direct reports. VP has 8 direct reports + 5 that report to AVP. The entire team is about 34. Benefits - Full Relocation Assistance Available - Yes Bonus Eligible - Yes Interview Travel Reimbursed - Yes AVP Evidence Lead Diabete...
Company Confidential East Windsor, NJ, 08520
Overview Responsible for testing of raw materials, establishing impurity and degradation profiles for active bulk drug substance and release testing of drug product produced using Aprecia Pharmaceutical’s proprietary technology. Description of Duties Research, design and create, QC friendly new procedure to achieve cost effective quantitative test methods. Perform analytical method development...
Johnson & Johnson companies are equal opportunity employers. Head of Clinical Development-0462140723 Description Janssen Diagnostics, L.L.C., a member of Johnson & Johnson's Family of Companies, is recruiting for a Head of Clinical Development located in Raritan, NJ. The Head of Clinical Development will serve as the primary point of contact and resource for development activities of diagnosti...
TechData is looking for Biostatistician (some can be telecommuting), SAS Programmer/Statistical Programmer (Some can be telecommuting), Recruiter, Project manager, Quality Assurance, Database Administrator, Drug Safety Specialist, Clinical Data Managerfor our pharmaceutical clients in Central NJ. Please see below requirements and send your resume to: *****. TechData is a l...
Ortho-Clinical Diagnostics is recruiting for a Manager, Worldwide Commercial Enablement, which is part of our Commercial Operations, and can be located off or on site, Rochester or NJ would be preferred. Ortho Clinical Diagnostics (OCD) is a leading provider ofin vitrodiagnostic products and services, offering accurate, timely, and cost-effective solutions for screening, diagnosing, monitoring an...
Requisition ID 25178BR Title In-House Clinical Research Associate (CRA) Job Category Clinical Trial Management Job Description PURPOSE: Responsible for the support of assigned sites in accordance with Good Clinical Practice (GCP), ICH guidelines, federal regulations and SOPs. Close collaboration with other members within Clinical Trial Management (CTM) and with various representatives within C...
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 ...
Job Responsibilities - Define global CMC regulatory strategy for ANDA filing of injectable products and manage the preparation, assembly and review of the quality (CMC) sections of regulatory submissions. - Liase with FDA in written communications - Coordinate responses to global regulatory agencies dealing with quality sections of global regulatory submissions Qualifications - At least bache...

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