R & D Jobs in South Plainfield, New Jersey

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233 South Plainfield, NJ R & D jobs found on Monster.

Jobs 1 to 20 of 233
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...
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...
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...
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...
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...
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...
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 ...
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...
Celgene is a global biopharmaceutical company leading the way in medical innovation to help patients live longer, better lives. Our purpose as a company is to discover and develop therapies that will change the course of human health. We value our passion for patients, quest for innovation, spirit of independence and love of challenge. With a presence in more than 70 countries - and growing - we l...
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...
Hays Life Sciences has partnered with a prominent global pharmaceutical client seeking a candidate who will be responsible for the development of formulations for topical products. Our client specializes in generic products for topical and oral administration. This person will need experience working with semisolid and liquid dosage forms. Additionally, this candidate will also be responsible for ...
Seeking a Product Development Manager with direct experience working with Semi-Solid, Solid and Liquid formulations. The purpose of this position is to direct the development of formulations and manufacturing processes of new products, including but not limited to the general oversight of all issues associated with guiding the development process from pre-formulations work to the manufacture of th...
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...
If you are interested in a GREAT contract opportunity to get your foot in the door with a top chemical company in the world please email a word .doc version of your resume to *****. This is an entry level role (No MS or PHDs will be considered) The successful candidate will perform a variety of routine chemical and physical tests for the Analytical Services and Materials Charact...
Company Confidential Berkeley Heights, NJ, 07922
We are eagerly reviewing new resumes and have 2 openings for Clinical SAS Programmers. Requirements: -Bachelor’s degree or higher in analytical field -At least five years of progressive SAS experience within a pharmaceutical setting. -Good knowledge of statistical terminology, clinical data structure , clinical tests, medical terminology, regulatory standards and protocol designs. -Strong SAS...
Company Confidential Berkeley Heights, NJ, 07922
• Responsible for conducted a comprehensive study feasibility assessment for new clinical trials. Ability to rather competitive intelligence data on the disease, standard of care, clinical trial and drug development landscape and then apply this foundational knowledge to develop predictive analytics for the new trial. • Collaborate with Clinical Research and Development Operations functions and c...
A Regulatory Affairs Specialist III (known hereafter as RA professional) provides regulatory expertise specifically in biologic and sterile product requirements and is able to expertly advise client or Catalent in identifying and executing the required development and regulatory activities needed to support the biological product development. This position executes projects independently under th...

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