R & D Jobs in Somerville, New Jersey

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205 Somerville, NJ R & D jobs found on Monster.

Jobs 1 to 20 of 205
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...
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...
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...
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 ...
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...
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...
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...
ESSENTIAL DUTIES AND RESPONSIBILITIES: Develops multiple processes in the laboratory, scaling up and overseeing the processes, according to cGMP guidelines and ISO 17025 requirements. Well versed in all USP microbiological testing, especially USP , , . Maintains laboratory policy and procedure manuals and assists in developing and writing procedures; validates the procedures and document prepar...
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...
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...
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...
Description The Global Surgery Group is comprised of the following businesses within Pharmaceutical client: Ethicon Surgical Care, Ethicon Energy, Ethicon Biosurgery, Acclarent, Biosense Webster, Cordis, Mentor and Sterilmed. With annual sales of $11 billion, the Global Surgery Group is the world’s largest, most innovative surgical company. The strength of the Global Surgery Group is illustrated ...
Johnson & Johnson companies are equal opportunity employers. Associate Engineer, R&D-9349141113 Description Ethicon, a member of Johnson & Johnson's Family of Companies, is currently recruiting for an Associate Engineer, to be located in Somerville, New Jersey. The Ethicon business offers a broad range of products, platforms and technologies-including sutures, hemostasis products, surgical sta...
Johnson & Johnson companies are equal opportunity employers. Staff Biostatistician-3404140827 Description Janssen Diagnostics, LLC, a member of the Johnson & Johnson Family of Companies, is recruiting for a Staff Biostatistician to be located in Raritan, NJ. Janssen Diagnostics, LLC, a Janssen Pharmaceutical Company of Johnson & Johnson, is the center of excellence in specialized diagnostics d...
Johnson & Johnson companies are equal opportunity employers. Associate Director, Critical Phase Program Manager-5999141007 Description Janssen Research and Development, LLC, a member of Johnson & Johnson's Family of Companies, is recruiting for an Associate Director, Critical Phase Program Manager to be located in either Raritan, NJ (preferred), Titusville, NJ or Spring House, PA. Janssen Rese...
Johnson & Johnson companies are equal opportunity employers. Regulatory Program Manager-9316141110 Description Janssen Research and Development, LLC, a member of Johnson & Johnson's Family of Companies, is recruiting for a Regulatory Program Manager to be located in Raritan, NJ; Titusville, NJ; or Spring House, PA. Janssen Research & Development, L.L.C. develops treatments that improve the hea...

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