R & D Jobs in Cranbury, New Jersey

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146 Cranbury, NJ R & D jobs found on Monster.

Jobs 1 to 20 of 146
Excellent opportunities for Quality Assurance personnel to join a rapidly growing R&D oriented service laboratory located in central New Jersey. Quality Assurance Auditor Responsibilities include but are not limited to: inspecting/auditing analytical/bioanalytical studies performed according to Good Laboratory Practices (FDA, EPA, and OECD); reviewing study data and reports; auditing software/sy...
. Adecco Engineering and Technical, a division of the world leader in the recruitment of engineering and information technology professionals, has an immediate opening for a QC Technician on a contract opportunity with a leading company in Plainsboro, NJ. The position is expected to last at least 3 months. In the position, the candidate would control, monitor, and report on quality during all ph...
Requirements: -Ph.D. and/or M.D. in medicine, pharmaceutical sciences, engineering, or a related field, with 2-5 years of industry experience in clinical pharmacology/pharmacometrics, and proficiency with S-PLUS/R and NONMEM software. -Strong oral and written communication skills to clearly present scientific data, its interpretation and significance, and the ability to work in a dynamic scienti...
We currently have an excellent opportunity for a Program Manager located at our Princeton, NJ office. The individual will lead the product engineering group as well as some product development projects from initiation through manufacture (launch). Responsibilities will include influencing and supporting Strategic Business Unit (SBU) decisions, resource allocation, budget tracking, process improv...
Requisition ID 23682BR Title In-House Clinical Research Associate (CRA) Job Category Clinical Trial Management Job Description PURPOSE: Responsible for the support of assigned sites in accordance with Good Clinical Practice (GCP), ICH guidelines and federal regulations. Close collaboration with other members within Clinical Trial Management (CTM) and with various representatives within CMR. Ma...
Requisition ID 23681BR Title Project Manager, Clinical Project Management Job Category Clinical Trial Management Job Description SUMMARY: Responsible for the operational and financial management of clinical trial planning and execution for assigned projects. Close collaboration with other members within Clinical Trial Management (CTM) and with various functional units of NNI as well as HQ. RE...
We currently have an excellent opportunity for a Chemist located at our Princeton, NJ R&D facility. The candidate for this position will be focused on development and improvement of new and existing fabric care products and activities supporting the Fabric Care/Laundry business. Roles & Responsibilities Perform hands-on product development activities, including laboratory experiments, sample pr...
OUTCOMES RESEARCH SPECIALIST REQUIREMENT #14-00895 RECRUITER: CHERYL AMBROSE JOB LOCATION: PRINCETON, NJ AUGUST 21, 2014 Project Description: Expected Areas of Competence Good understanding of Outcomes Research studies relating to health economics, epidemiology, Patient Reported Outcomes and quality of care. Ability to work with external groups academics and vendors starting with the RFP p...
This position coordinates and ensures effective and timely input into the planning, agreement and generation of required documentation, and the review and compilation of dossiers. Provide leadership to the Regulatory Associates, i.e filing procedures, and document retrieval. Scope · Responsible for strategizing activities at Ranbaxy/Ohm sites as well as 3rd party manufacturers. · Monitor all ap...
Scope This position supports the regulatory manager in day to day activities to ensure the timely compilation and submission of ANDAs, annual reports, amendments, supplements and deficiency responses to the FDA. Interact and provide support to other departments including, but not limited to, PDTS, Quality Assurance, Quality Control and Manufacturing. Responsible for timely preparation and submis...
We are currently looking for a Report Coordinator at our InVentiv Health Clinical Lab located in Princeton, NJ for a 6 month contract position. Job Responsibilities: · Become familiar with the policies and practices at the InVentiv Health Clinical Lab, including familiarity with computer systems, SOPs and LOGs that are pertinent to the employees duties · Know and follow all laboratory safety po...
Sr Associate Regulatory Affairs (CMC) Our client a global pharmaceutical organization is seeking a Regulatory Affairs Senior Associate to join their team. This is an exciting time to join this organization as they recently brought several new products to market. Great full-time permanent opportunity! Position offers tremendous growth, competitive compensation, comprehensive benefits and a reward...
W2 only! PLEASE ONLY RESPOND IF YOU HAVE BELOW SKILLS and are interested in a 6 month + contract. - Must have 7+ years experience as a director with pharmaceutical marketing experience - Bachelors Degree REQUIRED - Cardiovascular disease area preferred Responsibilities: - Partnering with R&D and business development - Focus on advancing early cardiovascular pipeline assets - Provide input i...
Global pharmaceutical company is seeking a Director or Vice President of Quality to join their team. We are looking for a forward thinking quality professional to maintain and build upon our quality approach to providing pharmaceuticals. The Director/Vice President is responsible for the site’s quality systems ensuring the connection with manufacturing processes and business to customer needs. Yo...
JUNIOR DOCUMENT PUBLISHER WITH SAP EXPERIENCE REQUIREMENT #14-00860 RECRUITER: NATALYA VOLKOV JOB LOCATION: NEW BRUNSWICK, NJ AUGUST 13, 2014 Project Description: Document publishers work with an integrated system of computer applications to manage, edit and publish documents for submission to health authorities around the world. The candidate should have excellent computer skills, including...
Company: Yoh An Analytical Scientist is needed for a long term contract with Yoh's client located in Cranbury, NJ. Top Skills You Should Possess: - Analytical methods and testing - Research and development - GMP What You'll Be Doing: - Perform either validation studies for analytical methods, conduct stability analyses on R&D drug product, or test of Raw Materials for Release - Execute cur...
Senior Research Scientist East Windsor, NJ Position Summary: Due to expansion of our activities and to strengthen our R&D team, we currently have a job opening for a senior research scientist at our East Windsor, NJ laboratories. The successful candidate will develop new additive products and technologies for the consumer markets. The senior research scientist will identify product opportunitie...
Responsibilities: XenoBiotic Laboratories, Inc. (XBL), a GLP-regulated Pharmaceutical Development Contract Research Organization located in central NJ, is seeking an experienced Post-Doc with expert knowledge of in vitro drug metabolism. The position requires a solid background and understanding of drug metabolism, drug-metabolizing enzymes, drug-drug interactions, and a wide variety of bioanalyt...
ASSOCIATE MANAGER/DATA ANALYST Minimum REQUIREMENTS: Job Description: Job Role and Responsibilities: The primary responsibility is to conduct specific in-house HEOR studies across the entire portfolio. In addition, the incumbent also coordinates certain department-wide activities including but not limited to HEOR website, staff meetings, HEOR Research Review Committee (RRC) meetings, and key c...
Company Confidential East Windsor, NJ
Aprecia Pharmaceuticals 1. Responsible for testing and release of finished pharmaceutical products, stability samples, raw materials, registration, clinical and marketed products batches under GMP/GLP environment as per company's standard operating procedures and USP/FDA guidelines. 2. Performs analytical method validation according to an approved method validation protocol and support analytica...

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