Cranbury
R & D Jobs in Cranbury, New Jersey
135 Cranbury, NJ R & D jobs found on Monster.
Yoh has a contract to hire opportunity for an Associate Scientist - Analytical / Formulations / Development Sciences tojoin our client in the Princeton, NJ area. Job Responsibilities: - Development, qualification, and implementation of analytical methods for protein therapeutics. - Design and implementation of experiments to investigate protein product quality attributes - Prepare all lab document...
Requisition ID 13372BR Title Principal Statistician/Assoc. Director - Biostatistics Job Category Medical Information Job Description PURPOSE: This is a senior level technical position. Work under minimal supervision, the incumbent is responsible for the delivery of statistical support to NN's clinical development, registration, and marketing support programs. Functions include clinical trial desig...
Manager of Medical Information Through decades of combined experience, CSG, Inc. understands the intricacies of the drug development process, industry-based technologies, and the responsibilities tied to the positions we support. This has helped our firm gain credibility and notoriety with key decision makers within Pharmaceutical companies ranging from small start-ups to fortune 500 corporations....
We have several openings for Laboratory Assistants & Entry-level associate scientists to join a rapidly growing R&D-oriented service laboratory in central New Jersey in the areas of Animal Science and Bioanaltyical/Metabolism/Pharmaceutical Chemistry. Laboratory Animal Science Assistant The successful candidates must have a High School and or Associates degree with experience to work on in-life ph...
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/syst...
Job Title: Global Clinical Study Manager Position Description Oversee Phase IV and PMS studies to support multiple brands in CV-Met, Immuno, Virology and Neuroscience. Position Responsibilities Demonstrates a strong operational understanding of conducting clinical trials. In conjunction with Medical Strategy and Field Medical Science (FMS) executes or oversees outsourced Phase IV and Post Marketin...
CHEMIST (Multiple Opportunities) Keywords: entry-level, chemistry, chemists, scientist, lab tech, lab technician, science, biology WILL TRAIN ENTRY LEVEL CANDIDATES! Accutest Laboratories is a nationwide environmental testing laboratory that has successfully delivered defensible data for over 50 years. Founded in 1956, Accutest is the nation’s 3rd largest environmental testing laboratory combining...
GENERAL DESCRIPTION: Supervise and assist in the conduct of regulatory studies performed at Product Safety Labs (PSL). Responsibilities include: Supervise study conduct. Assist in protocol development, design and implementation. Responsibilities as stated in GLP regulations. Data interpretation and report writing. Client liaison. QUALIFICATIONS: M.S. degree in Chemistry with at least 5 years relat...
Large pharmaceutical company in Central NJ has an immediate need for a contract based SAS Programmer. Role is approved through year end with the option to be extended. Prefer MS level grads, but will consider BS level candidates. Prospects must possess 5+ years of SAS programming experience within an Outcomes Research or Analytics department within a sponsor or specialty firm. Candidates must have...
REQUIRED • Must be Pharm.D. with 3-5 years pharmaceutical industry experience or relevant clinical experience 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 staff when discussing products....
Environmental Project Manager Insurance Restoration Specialists, Inc. (IRS) is a turnkey environmental company seeking a Project Manager licensed with the NJDEP for Subsurface Evaluation & Tank Closure. Candidate will complete a wide array of tasks for each project from cradle to grave. Everyday tasks may include site inspections, job estimation providing cost estimates and proposals, supervising...
Job Title: Clinical Trial Associate Position Description Supports project clinical teams by performing tasks related to study mgt from start up to study completion. Distributes, collects and tracks study documentation and completes project deliverables accurately and within project timelines. Key role in supporting project team needs. Utilizes technology effectively to support clinical development...
Company Confidential
Princeton, NJ
Senior Research Scientist: The major duties and responsibilities of a Senior Research Scientist include the following: 1. Follows all standard operating procedures, safety and security polices and prescribedGLP and Biomarker and Immunoanalytical Division practices, policies and guidelines; use SOP manual as reference to support work performed. Completes all necessary paperwork related to job dutie...
Company Confidential
Princeton, NJ
Senior Technical Director - Biotechnology expertise Primary responsibility for overall Scientific Strategy, capabilities and technology used at all sites. This includes: * Overall responsibility for content for presentations, technical papers, conference and trade show attendance for company. * Leading position representing company ‘s technical capabilities in client visits. Management of Technolo...
Shall design and develop dosage forms for metered dose inhalers, dry powder inhalers, nasal sprays, and nebulizers. Required Experience: * Design of Experiments. * Solid state characterization: HPLC, UV-VIS, FTIR, Raman, X-ray Powder Diffraction, thermal analysis. * Aerosol and powder characterization: cascade impaction, moisture sorption isotherm, bulk density, surface area, particle size analysi...
Shall design and develop formulations of new transdermal products. Required Experience: * Transdermal patch physical property testing and rheology testing * Transdermal characterization: x-ray powder diffractometry (XRPD), differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), and isothermal microcalorimetry (ITMC) * Knowledgeable of scale-up, tech transfer, and process optimiz...
Company Confidential
Princeton, NJ
Job Responsibilities: The Bioinformatics Data Manager will have primary responsibility for the Bioinformatics data lifecycle. S/He will actively manage data exchange with collaborators, leverage both community data and data standards for internal use and develop/adopt/utilize common ontologies to categorize data. S/He will ensure data integrity and the consistency of meta-data across scientific sy...
Regulatory Affairs Associate Princeton, NJ Our client, a global pharmaceutical organization is seeking a Regulatory Affairs Associate to join their team. This position will be part the Regulatory Affairs Department and NDA submissions team. This is an exciting time to join this organization as they recently brought several new products to market. Position offers tremendous growth, competitive comp...
Currently we have a temporary opening for a Quality Assurance Specialist to support a company located in the Princeton, NJ area. Responsibilities: Write pharmaceutical manufacturing batch records. Process validation protocols and reports. Process development and scale-up reports. Update SOPs pertaining to manufacturing which requires an understanding of manufacturing processes for oral solid dosag...
Company Confidential
Princeton, NJ
Description Working in collaboration with global regulatory and safety (GRS) CMC teams and bioprocess manufacturing/process development technical experts. Creates final drafts of Regulatory documents for submission to GRS and onwards to global Health Authorities. Documents included: BLA, MAA, IND, IMPD, Briefing packs, responses to queries. Develops overall document strategy with GRS and CMC leade...
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©2013 Monster - All Rights Reserved U.S. Patents No. 5,832,497; 7,599,930 B1; 7,827,125 and 7,836,060 MWW - Looking for Monster Cable? - V: 2013.1.5.22-218