R & D Jobs in Morristown, New Jersey

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155 Morristown, NJ R & D jobs found on Monster.

Jobs 1 to 20 of 155
Job Responsibilities: This position will provide expert guidance and leadership to the Product Stewardship and Toxicology function, business leaders and technology developers regarding risk assessment for all stages of a product's life cycle. As well as work with external regulatory agencies like to EPA and FDA regarding risk assessment for all stages of a chemical product's life cycle. Key member...
Company Confidential Matawan, NJ, 07747
The Senior Fragrance Development Manager is responsible for developing creative strategies and leading large (global) projects. He/she will need to further develop business knowledge and technical expertise in order to increase the ability to win in the market place. In addition, this role will need to leverage internal processes/programs/tools to support overall business strategy. In addition he/...
The goal of this position is to participate in ongoing research in the development of flavors and fragrances that provide IFF with new opportunities for profitable growth. In this role, the successful candidate will be responsible for managing sensory projects to support and guide the creative and technical teams, including development and implementation of current and new sensory science methodol...
Controls Engineer for the rolling mill within a mini-mill operation located in Sayreville, NJ. Must have automation, controls, PLC, drives, and etc., in a high speed heavy manufacturing environment. Relocation paid. Responsibilities for the Controls Engineer Responsible for leading process controls and process improvements as they relate to automation and controls in a rolling mill setting. Act as...
The Operator 2 is responsible for operating and maintaining equipment for the treatment of wastewater, at a small wastewater treatment facility in Staten Island, NY. Provides routine testing, monitoring, and maintenance of production wells - Performs treatment process and maintenance of treatment facility equipment to assure proper operations - Conducts routine sampling and field testing of water...
On behalf of Research Triangle Institute, Headway Workforce Solutions is seeking part time Field Staff to work on a government sponsored research study in Monmouth County. 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, sponsored by the National Oceanic and...
We are looking for qualified Registered nurses ,foreign medical professionals and professionals with background related to pharmacy in the area of Pharmacovigilance against firm job requirements. If interested, please apply with your updated resume immediately as we have many positions to be filled....
Medical Director, US Medical Affairs: Top 20 Oncology Drug to Treat Multiple Tumors Summary: You will be the US Lead MD/Physician for a Top 20 Oncology drug that treats multiple tumors/cancers as a mono and combination therapy. This is a very visible and challenging position with a Top Global Pharmaceutical/Biotechnology Company that has multiple top 20 drugs to treat solid tumors and blood cancer...
Due Diligence for Health Care Business Integrity Program Department: Worldwide Transportation Reports to: Director of Global Trade Compliance Location: Piscataway, NJ; meetings possible in various NJ locations Qualifications project management; communications and organizational skills Education: BA Experience: at least 5 years project management; transportation and regulatory compliance knowledge;...
TRG has recently been engaged by one of our top clients located in New Jersey, a rapidly growing and respected Pharmaceutical organization that is actively seeking qualified candidates for the role of DIRECTOR/SENIOR DIRECTOR OF REGULATORY AFFAIRS to help them with the development of their cutting edge portfolio of pharmaceuticals. ADVANTAGES OF THIS OPPORTUNITY: CHANCE TO MAKE A DIFFERENCE – As t...
Email resumes to ***** or call me at 732 429 1850 asap Direct Client -Generic Pharma Client Location- Piscataway,NJ Fulltime/Permanent Role Salary-$ 150k Experience: -At least 10-15 years experience in filing IND’s, 505b(2) and ANDA’s for injectable, ophthalmics and solid dosage forms -Assembling documents for eCTD filing -Compiling eCTD filings using appropriate software -interact...
Must have: Strong Phase III regulatory writing experience AND PK/PD Phase I writing experience Therapeutic area experience in: oncology and/or endocrinology Duties and Responsibilities % of Time Provide medical writing support for development programs by hands-on writing of protocols, IBs, and CSRs. Participate in appropriate development teams and internal strategy and operations meetings. 60% Man...
Seeking an experienced company's Rave study builder who can work at our Edison, NJ location. Key Responsibilities: • Advise external customers and internal staff on best practices for implementing Company's software • Work with Project Managers in translation of customer needs in terms of system functionality to ensure a match between needs and actual system capabilities/limitations • Work directl...
FULL TIME POSITION in METUCHEN NJ (Must have Pharma Experience) Senior Business Analyst proactively assesses upcoming changes in the regulatory, industry and business environments in the field of Clinical Repositories, Clinical Operations, Clinical Data reporting, dashboards, metrics, Analytics, and trial management reporting. Supports the creation of roadmaps for customers Participate in Requirem...
We have partnered with a large company in Monroe, NJ area to provide them with Associate Drug Safety Monitor on a long term contract basis Duration: 24 Months Description: · The occupant of this contractor position provides support to the Drug Safety Monitor in gathering information and quality control during the processing of serious and non-serious adverse event (AE) reports regarding Client pro...
Summary: The Associate Director, R&D Medical Applications leads development and day-to-day production support for new and existing global solutions supporting Global Medical & Regulatory Affairs (GMRA) , Group Quality and the R&D departments. Primary application areas include Clintrace and MedDRA, Trackwise and Documentum (Expresso). Manages the planning and implementation of complete business sol...
Job Description 6 month contract opportunity with a Best in Class company in the Chemical Industry that's seeking a Lab Technician to assist / support a hydrocarbon testing process within a program called "Refinery Returns". Job Duties · Testing · Operate a variety of testing equipment · Interpret test results and assess validity and reliability of data · This is a support role that is attached to...
The Chemist will be responsible for the site’s chemical inventory management system. The Chemist will also be responsible for managing wastes, both hazardous and non-hazardous, for the site. In addition, this individual will be cross trained on other functions in the R&D Services Department. MAJOR RESPONSIBILITIES: · Along with site EHS representative, lead the site’s initiative to comply with new...
Accriva Diagnostics is a leader in the development and manufacturing of Point-of-Care diagnostics. 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 are currently hiring several temporary QC Technologists for our Edison, NJ location. SUMMARY: The QC Technol...
Microbiology Analyst role available with renown Pharmaceutical Services company's Edison, NJ location: Minimum 1 year in a cGMP facility performing USP Microbiology testing Minimum BA/BS degree in Microbiology or related Hands on with common USP Microbiology tests: o USP and Microbial Limit Tests o USP Antimicrobial Preservatives-Effectiveness o USP Antibiotics o USP Endotoxin o USP Sterility...
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