R & D Jobs in North Brunswick, New Jersey

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

Jobs 1 to 20 of 350
Assist Director of Compliance with batch record review, labeling artwork, FDA filings related to MedWatch, Annual /Quarterly reporting, and promotional materials. Knowledge of FDA Regulations, familiar with USP/NF , eCTD format, ANDA compilation. Ability to develop SOP’s, conduct GMP/laboratory audits, and handle customer complaints. Candidate must be detailed oriented, and have excellent communic...
HISTOLOGY TECHNICIAN - MUST HAVE ANIMAL TISSUE EXPERIENCE!!! JOB RESPONSIBILITIES: Prepare histologic slides from tissue sections for microscopic examination and diagnosis by the Pathologist. Prepare sections of lab animal tissue for immediate examination, using rapid tissue processing and frozen section technique to freeze, cut, mount and stain tissue specimen received from animal necropsies. ...
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...
We have an opening for a formulations chemist, Pharmaceutical Formulations - Dry Powder - Aerosols in the Dayton, NJ Area. Responsibilities for Formulations Scientist - Dry Powder - Aerosols • Blend dry powder formulations, operation / assembly / cleaning of mixing equipment, transferring of formulations from one type of container to another, conditioning experiments / working with analytical su...
POSITION SUMMARY: Primary Function: Processes, performs and results medical diagnostic testing on body fluids by automated and manual methods in a timely manner under the supervision of the senior technologists. Produces medical diagnostic test results in an efficient and cost effective manner for stat and routine specimens. Maintains, troubleshoots and repairs instruments and lab equipment if pos...
POSITION SUMMARY Primary Function: Maintains positive patient identification while procuring venous and capillary blood specimens on all patients regardless of age on a routine and stat basis. Verifies orders from scripts and orders procedures in HIS and LIS. Follows established procedures for patient identification and specimen labeling. Performs accessioning and clerical duties as needed. Set-u...
CorePharma LLC is a fast growing mid-size generic pharmaceutical company with approximately 270 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 primary role of the QA Project Manager is to support a launch process by coordin...
MEDICAL INFORMATION MANAGER REQUIREMENT #15-00106 RECRUITER: MICHELLE ASHEN JOB LOCATION: PLAINSBORO, NJ JANUARY 29, 2015 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 professional staf...
If you’re interested in working for a Leading, Mid-Size Contract Research Organization (CRO) that has a massive global reach, then look no further, because Pharm-Olam International offers all of that and more! We are a company that strives to deliver cost-effective, quick-to-market clinical services in today’s emerging marketplace. Pharm-Olam International (POI) has one of the largest global footp...
Regulatory Affairs Specialist (CMC) Kelly Scientific has been retained to locate a Regulatory Affairs Specialist (CMC). This is an amazing opportunity with an up and coming company in Central NJ. The responsibilities of this individual will be to combine their knowledge of scientific, regulatory and business issues to enable generic pharmaceutical products that are developed, manufactured and dis...
Job Title: Senior Scientist/Engineer in Upstream Process Development Required Skills: fermentation, CHO cell culture, microbial fermentation, process development/design, molecular biology, mammalian cells, DNA construction, early discovery & late discovery stages, biologics, small molecules and Biosimilars Qualification & Experience: A MS/PhD degree with 2 - 4 years with hands-on experience in ...
ARMD Team Lead/Mgr Responsibility: Responsible for managing the research and development activities in the Analytical Research and Methods Development Department in support of ANDA submissions and providing technical guidance to the group. Reports to the Director, Analytical Research and Methods Development. Work Performed: 1. Provides guidance for the development of analytical methods that inc...
Job Title: Senior Chemist Responsibilities: Responsible for the development and validation primarily of stability-indicating analytical methods applicable to specific pharmaceutical products. Work Performed: • Conduct analysis of Finished products, Stability, Raw materials using equipment such as HPLC, GC, FT-IR, UV, Karl Fisher • Perform analysis of Residual Solvents and Impurities for Drug ...
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...
NNIT US is seeking talented consultants to support our ambitious growth aspirations within Life sciences consulting. The pharmaceutical industry is experiencing a radical change in their core business in terms of efficient exploitation of IT and use of new technology platforms. We therefor seek new colleagues to join our Life sciences consulting team focusing on Regulatory Affairs. The positions...
Manager, Regulatory Affairs (Labeling) Perm Opportunity Our Client a Global Pharmaceutical Company is seeking a Manager, Regulatory Affairs (Labeling) to join their team. In this critical role, you will ensure regulatory compliance in relation to Labeling and Promotional Review submissions and initiatives. Knowledge of OPDP is critical as is Generic Pharma Products. Position offers competitive c...
At Dr. Reddy’s, a global pharmaceutical company, you will contribute to making the breakthroughs of tomorrow a reality today! From making medicines more affordable to discovering innovative treatment options to satisfy unmet medical needs, we are dedicated to helping people lead longer and healthier lives. We are seeking dynamic and energetic individuals ready to inspire, ready to make a differenc...
inVentiv Health – Transforming Promising Ideas into Commercial Reality Job Title: Study Start-Up Specialist II Location: Princeton, NJ Job Description: · Research local requirements for documentation of IRB / EC submission approvals, and subsequent follow-up documentation · Liaise with study sites regarding essential document collection and, as required by country, site contract/ budget negot...
inVentiv Health – Transforming Promising Ideas into Commercial Reality Job Title: Manager, Study Start-Up Location: Princeton, NJ Job Description: · Provide project support, performance management, and career development guidance to direct reports · Coordinate new employee onboarding orientation and training at the department level · Assess, track and manage employees activities to ensure de...
Our client is seeking a Technical Support Specialist for a contract to hire position in Edison, NJ. The candidate is a well rounded individual who has the ability to thrive in a high pressure environment while maintaining high quality and proper communication. The Technical Support Specialist has the ability to quickly learn different applications and technologies and apply that knowledge to resol...

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