R & D Jobs in North Brunswick, New Jersey

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251 North Brunswick, NJ R & D jobs found on Monster.

Jobs 1 to 20 of 251
Accountabilities: The Auditor is accountable for review of data (submission/ pre-submission data that goes to FDA) critically per current in-house and compendia requirements to ensure completeness and accuracy of the data. There is heavy penalty for non-compliance of activities laid down in consent decree. · Depending upon submission (Annual review, ANDA, NDA, CBE, PAS, Response to FDA deficienc...
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...
IBA Molecular, a global leader in the radiopharmaceutical industry, is dedicated to delivering the best products, and services in the fields of personalized medicine, molecular imaging and nuclear medicine. With our corporate headquarters in Dulles, VA and locations throughout the US and Europe, IBA Molecular’s global presence serves customers throughout the world. With over thirty years of manufa...
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...
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...
Are you a chromatographer who enjoys the challenge of method development, solving problems and working on daily challenges but wants to escape the monotony of pipetting? Do you enjoy scientific research but find the laboratory life less than satisfying lately? Would you like to remain involved in HPLC/GC/SPE AND see new labs, help solve method problems, deliver new technologies to customers and ...
TechLaw, Inc., a nationwide Environmental Consulting firm, seeks chemists and biologists of all levels for Environmental Services Assistance Team contract supporting U.S. EPA laboratories located in Edison, NJ. Experience with organic and inorganic laboratory equipment, laboratory procedures, sample extractions, and EPA analytical methods are desired. Candidates must have at least a BA/BS degree...
CorePharma LLC is a fast growing mid-size generic pharmaceutical company with approximately 250 employees, located in Middlesex, New Jersey. We are a fourteen year old firm principally in the business of developing, manufacturing, and distributing pharmaceutical products for the United States market. JOB SUMMARY: Under the direct supervision of the Supervisor, Quality Control Laboratory, the inc...
Intellisphere, LLC a Princeton, NJ-area medical publisher is looking for an experienced professional with clinical and communications experience to provide support and oversight for editorial projects covering a wide variety of publication properties. Projects span a variety of therapeutic areas including cardiology, endocrinology, oncology, psychiatry and others. Additionally, this position assis...
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...
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 Post-Doc with expert knowledge of Bioanalysis of analytes and its metabolite...
GLOBAL CLINICAL PROTOCOL MANAGER - LATE PHASE SPONSORED RESEARCH WITH ONCOLOGY REQUIREMENT #14-00927 RECRUITER: CINDI PISNOY JOB LOCATION: PLAINSBORO, NJ SEPTEMBER 2, 2014 Expected Areas of Competence: General · Manages successful execution and completion of assigned global clinical Phase IIIb/IV publication/medical informing trials within CSR&O Late Phase Sponsored Research unit, in adhere...
At Joulé, you could say the right match is in our DNA. We're the specialists in Scientific Staffing. Our unmatched industry network and geographic reach enable us to place professionals like you at top firms every day. For more than 20 years, we've been providing temporary, contract and direct staff to pharmaceutical, biotechnology, food, flavor and fragrance, specialty chemical and other scientif...
MEDICAL INFORMATION COORDINATOR REQUIREMENT #14-01197 RECRUITER: KAREN GULUTZ JOB LOCATION: PRINCETON, NJ NOVEMBER 11, 2014 Project Overview: · Partner with the Global Medical Team (GMT) Lead to facilitate the development and execution of Medical Plans for assigned products. Ensure Medical Plan is aligned with TA portfolio objectives/strategies · Build relationships with key stakeholders, i...
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...
inVentiv Health – Transforming Promising Ideas into Commercial Reality Job Title: Director, Document Management & Publishing Job Description: · Direct operations of the Document Management and Publishing, group · Provide regulatory consulting services to clients, in particular with respect to document management, archiving, and electronic publishing · Provide information and/or data to Propos...
POSITION SUMMARY: This isa full-time or contract position responsible for overseeing all clinical trial activities from start to finish for US and International studies. This includes trials necessitated by R&D, Regulatory and Marketing. ESSENTIAL DUTIES AND RESPONSIBILITIES: Manage clinical study monitors and interact with investigational sites. Oversee and Manage Contract Research Organizati...
Quality Assurance Operations Manager Beta Pharma, Inc. is seeking a skilled Quality Assurance Operations Managerto supportour office needs. The successful candidate will develop, implement, and oversee quality activities in support of GxP activities conducted or monitored by Beta Pharma, Inc. Beta Pharma, Inc. is an emerging specialty pharmaceutical company dedicated to the discovery, developmen...
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...
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...

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