R & D Jobs in East Brunswick, New Jersey

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89 East Brunswick, NJ R & D jobs found on Monster.

Jobs 1 to 20 of 89
Works with guidance from senior staff members develops formulations for a variety of dosage and delivery forms that support new products or product/process optimization projects. Prepares stability, consumer, and clinical samples as needed. With minimal supervision, run and monitor benchtop, pilot, and manufacturing scale-up and verification batches. Require Hands on experience or knowledge to o...
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...
Growing Pharmaceutical client in Central/Northern NJ area is looking to fill a temp-to-perm role for a Director, Quality Assurance/Auditing with large molecule, biologic experience. This job will have the following responsibilities: ·Manufacturing is done on-site, so client needs a hands-on leader to oversee QA and internal audit compliance. ·Primarily GMP, but some GLP and GCP oversight as wel...
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...
One of the world’s leading chemical companies has a job opening in their central New Jersey location. The company seeks a research engineer with a degree in Chemistry or Chemical Engineering to work on experimentation related to catalysts that reduce harmful emission gases. The company designs and develops catalysts and adsorbents used to treat and purify emission gases from power plants, or from...
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...
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...
The Quality Assurance department plays a critical role in the daily operations of the facility. The primary function of the department is to ensure compliance with c-GMP, domestic and international, as well as direction and oversight of internal quality systems requirements for the facility. The department is entirely separate from and independent of the personnel engaged in the direction and cond...
This a terrific opportunity for an Investigation Associate with a niche generic pharmaceutical company engaged in the manufacturing of multi-source and branded pharmaceuticals for pain management and anesthesia in the United States and across the globe. This ever growing company is looking for an Investigation Associate to come on board to their NJ facility. SUMMARY: Reviews, coordinates, and as...
Director, Research Toxicology PERM position, Mercer County NJ Small, growing, and reputable biopharmaceutical company in Mercer County, NJ is looking for a permanent Director, Research Toxicology. The Director of Toxicology is accountable for drug safety support for all programs in preclinical or clinical development. The individual will demonstrate competency in interpreting toxicology data, d...
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...
PLEASE EMAIL RESUMES TO ***** Client- Pharma Location- South Plainfield, NJ Duration- 3 m contract to Hire Protein Chemistry background. MS/Ph.D. Not required. Below are some of the Duties and Responsibilities. Perform QC chemistry testing for research and clinical batches. Perform stability testing for research and clinical batches. Execute method validation activities in ...
FIELD MEDICAL MANAGER REQUIREMENT #14-01148 RECRUITER: BRIDGET BURNS JOB LOCATION: PLAINSBORO, NJ OCTOBER 17, 2014 Project Description: Position supports the function of Field Medical working both within a therapeutic area(s) and with impact across the function of Field Medical to support the safe and appropriate use of the client’s medicines. Responsibilities Include: Provide assistance in...
MEDICAL INFORMATION MANAGER, FLUENT IN FRENCH REQUIREMENT #14-01062 RECRUITER: MICHELLE ASHEN JOB LOCATION: PLAINSBORO, NJ SEPTEMBER 29, 2014 Project Description: Participate in ongoing comprehensive product / disease area training to serve as Medical Information expert within area of responsibility Ability to communicate on professional level with physicians, nurses, pharmacists, and other...
MUST HAVE: -Must be Pharm.D. with 3-5 years pharmaceutical industry experience -Individual must have appropriate training and sensitivity to legal and regulatory issues for medical information, while meeting compliance standards for Medical information. -Microsoft Office skills -Understanding of specific disease state and pharmacotherapy knowledge in area(s) of responsibility Responsibilities...
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...
CorePharma LLC is a fast growing mid-size generic pharmaceutical company with approximately 250 employees, located in Middlesex, New Jersey. We are a fifteen year old firm principally in the business of developing, manufacturing, and distributing pharmaceutical products for the United States market. JOB SUMMARY: The QCCM, under the supervision of the Associate Director of Quality Systems andRegu...
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...
Job Description Analyze laboratory samples (raw material, in-process, finished product, stability, etc. Participate in laboratory investigations when required Service laboratory equipment (calibrations, preventative maintenances, etc.) Participates in the development of other Chemists (train, mentor & guide) Comply with all applicable OSHA Safety and Health Programs Adhere to all applicable ...

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