R & D Jobs in Trenton, New Jersey

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157 Trenton, NJ R & D jobs found on Monster.

Jobs 1 to 20 of 157
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...
QUALITY CONTROL, SUPERVISOR Bio-Pharm Inc. is a leading manufacturer and supplier of generic pharmaceutical formulations. This position is responsible for activities relating to the daily function of the Quality Control laboratory and strategic planning for the laboratory and laboratory staff. The individual is the subject matter expert on analytical testing. The individual is heavily involved in...
QUALITY CONTROL ANALYTICAL CHEMIST Bio-Pharm Inc. is a leading manufacturer and supplier of generic pharmaceutical formulations. Reporting directly to the Quality Control Manager, the Analytica Chemist will coordinate with other Quality Control chemists, R&D researchers and formulation specialists and other manufacturing departments to ensure high quality standards are always met. Major Tasks, K...
Job Description We are seeking a Director of Quality for a cGMP manufacturing and cGMP bioconjugation lab in Southeastern Pennsylvania. The candidate should have extensive experience in assuring cGMP compliance in a contract research organization that manufactures API's for clinical trials as well as overseeing a QC lab. The Director will be involved in daily operations and decision making, worki...
Johnson & Johnson companies are equal opportunity employers. Senior Analyst Incentive Compensation-2765140619 Description Janssen Pharmaceuticals, a member of the Johnson & Johnson Family of Companies, is recruiting for a Senior Analyst – Incentive Compensation to be located in Titusville, NJ. Janssen Pharmaceuticals, Inc., a pharmaceutical company of Johnson & Johnson, provides medicines for ...
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...
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...
Pharmacy Specialist Prefers a Bachelor's degree from an accredited college or university in Health Care Management, Business or Pharmaceutical Administration. Requires two (2) years experience in third party prescription program claim adjudication. Requires two (2) years experience as a Pharmacy Utilization Management Specialist. Requires prior customer service/service quality initiative exper...
Johnson & Johnson companies are equal opportunity employers. Senior Director, Woman's Health, Established Products Portfolio, Compound Development Team Leader-00000QGT Description Janssen Pharmaceutical Research & Development, L.L.C., a member of the Johnson & Johnson Family of Companies, is recruiting for a Senior Director, Womens Health, Established Products Portfolio/Compound Development Tea...
Research Scientist ELISA method development in GLP Also seeking: Immunoassay Project Manager in Maryland Also seeking in NC, Utah and NJ: Bioanalytical Lc/ms/ms Project Manager / Principal Investigator NJ Research Scientist: The major duties and responsibilities of a Research Scientist include the following: 1. Follows all standard operating procedures, safety and security polices and prescr...

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