R & D Jobs in Somerset, New Jersey

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191 Somerset, NJ R & D jobs found on Monster.

Jobs 1 to 20 of 191
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...
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...
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...
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. Staff R&D Engineer-9583140428 Description Mentor, a member of Johnson & Johnson's Family of Companies is currently recruiting for a Staff R&D Engineer, to be located in Somerville, New Jersey. Mentor Worldwide L.L.C., is a trusted global leader in aesthetic medicine among both consumers and clinicians by providing a broad range of in...
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...
Johnson & Johnson companies are equal opportunity employers. Manager, Quality Monitoring & Compliance-00000UH5 Description Janssen Research & Development, L.L.C., a member of Johnson & Johnson's Family of Companies, is recruiting for a Manager, Quality Monitoring & Compliance. The position will be based at one of the following R&D Q&C sites: Raritan, NJ; Titusville, NJ; Spring House, PA; Malver...
Responsible for day to day support of Quality Control (QC) activities for biological and/or small molecule projects to support US and international drug development and commercial programs. This includes performing data review, data and document management and working with CLOs to facilitate and assist in managing the timely testing and receipt of QC deliverables. Data Review - • Perform thoroug...
JOB SUMMARY: The Document Control Specialist will assist with the Document Control process. This role will serve as a Document administrator to track and monitor controlled documents throughout their lifecycle with emphasis on compliance to SOPs and applicable local Regulatory requirements. The role will support the various business functions in the organization for the timely and accurate genera...
Job Number: 424670 SAS Programmer 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 an ...
AkzoNobel is a leading global paints and coatings company and a major producer of specialty chemicals, with leading market positions and brands in countries around the world. We operate in a number of important market segments ranging from buildings and infrastructure to transport, industrial and consumer goods. We’re also the sector leader in sustainability and are number one in the renowned Dow ...
Our client is one of the to pharmaceutical companies in the world, looking for a Senior manager/Product Lead of Regulatory Affairs. This is a full time, permanent position in Bridgewater, NJ. Summary: The Regulatory Affairs Product Lead (RA PL) Senior Manager coordinates and manages all regulatory aspects for the Rx Branded products in their portfolio. He/She acts as the RA Product Lead and rep...
Responsibilities: · Excellent employment opportunity for a Regulatory Affairs Consultant in the Somerville, NJ area. · Work in cooperation with company personnel who maintain ultimate direction over the work. · Support U.S., EU, and International regulatory affairs activities for Project Complexity. · Collaborate with cross-functional project team members and commercial partners to oversee the...
Assisting R&D Chemists with lab samples batch preparation and stability sample testing. Responsibilities: Perform stability testing to monitor physical and chemical characteristics of aerosol products Daily interaction with R&D Chemists to make sure all out-of-spec results are investigated Document results of testing in accordance with GMP and FDA regulations Assist R&D team with gathering ne...
Senior Regulatory Manager Requirements: -Bachelor’s degree in science or health related field required; Advanced degree preferred (PhD, MD, PharmD, or equivalent) -6-8 years relevant pharmaceutical industry and regulatory experience -Documentum is a MUST; eCTD (electronic common technical documents) is a MUST -Biologics experience preferred but not necessary Responsibilities: -Develop a pro...
Our client is the world's leading chemical company. With more than 110,000 employees, six affiliate sites and approximately 380 additional production sites worldwide they serve customers and partners in almost all countries of the world. They combine economic success, social responsibility and environmental protection. Through science and innovation they enable customers in almost all industries t...
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...
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...
Principal Investigator / Project Manager positions Lc/ms/ms Project Managers in Utah and NC Immunoassay (large molecule) Project Managers in Maryland Are you a Sr. Scientist with CRO or client liaison experience? Will you relocate? 1. Bioanalytical Principal Investigator in Utah, New Jersey and North Carolina (also seek Sr. Scientist in NJ and NC) Must have Lc/ms/ms Method Development Experi...

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