South Plainfield
Biotech Jobs in South Plainfield, New Jersey
186 South Plainfield, NJ Biotech jobs found on Monster.
GENEWIZ, Inc. is an award-winning global contract research organization (CRO) specializing in DNA services. Excelling in both science and customer support, GENEWIZ is a trusted provider for DNA sequencing, gene synthesis, molecular biology, genomic, next generation sequencing, bioinformatics, and GxP/CLIA regulatory services. Customers depend on GENEWIZ to achieve results in a rapid, cost-effe...
Education: Associates or BA/BS Experience: Regulatory in Pharma or CRO Summary: Provides submission compilation, filing and archiving expertise in the acquisition, quality control, retention, and submission of nonclinical, CMC, and clinical regulatory documents and other sponsor-specific essential documents. Maintains electronic and hardcopy files, assures completeness of the records, and helps en...
ITC is a world leader in the development and manufacturing of Point-of Care blood coagulation and clinical diagnostic systems. We are committed to developing, manufacturing & marketing safe, easy to use, & reliable products that are used by doctors, nurses & medical practitioners where care is provided to patients. We currently have an opening in for a R&D Engineering Managerin our Piscataway loca...
Lead Clinical Data Manager – Full Time Permanent position in Metuchen, NJ All work to be performed onsite. For additional details please email me your resume at – arati.kapileshwari@maxisit.com Must have 3 yrs of Oncology experience and total of 6-7 years of Data Management experience · Require MediData Rave experience. · e/CRF Design – Review and approve CRF design, data review ground rules and d...
This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. Our Senior SAS Programmer Analysts play a key role within ICON developing and executing execute statistical programs designed to analyze clinical trial information. The Senior SAS Programme...
Job_Other_Compensation: We have an immediate need for a Chemist ESSENTIAL DUTIES AND RESPONSIBILITIES: Ability to perform all test procedures and handle instrumentation/equipment used in testing which includes Gas Chromatographs, UV-Visible Spectrometers, titrators, Melt Flow Indexer, various particle size determination techniques and classical lab apparatuses. Perform polymerizations and physical...
Croda Inc is a world-class leading supplier of high quality, innovative specialty ingredients used in the personal care, pharmaceutical, household, and industrial markets. The culture of Croda Inc is one that values and respects the individual and their contribution to the Company’s results. Our aim is to provide a safe work environment where employees are encouraged to communicate with management...
Requirements: Bachelor's degree Experienced CRA with 5+ years of recent direct monitoring Must have strong inpatient hospital chart/EMR experience 3 plus years of Oncology monitoring required Inpatient monitoring experience Travel is expected to be, on average, 75%, sometimes more depending on trial demands. Must have home office Phase II-III trial experience...
Part Time Field Staff Needed On behalf of Research Triangle Institute, Headway Workforce Solutions is seeking part time Field Staff to work on a government sponsored research study in New Brunswick, NJ. Candidates must live close to the coast. POSITION SUMMARY RTI International is seeking to hire field interviewers for the Access-Point Angler Intercept Survey. This important research study, sponso...
The Scientist will be part of a team of drug development professionals responsible for the continued development and regulatory approval of thin film drug products containing a wide range of therapeutic compounds. Responsibilities: · Conduct laboratory activities and formulation work in support of product development, product characterization and process optimization relating to MonoSol Rx Pharmac...
This position is responsible for the management, development, implementation and coordination of regulatory affairs with a focus on understanding, implementing and insuring compliance with global quality/regulatory requirements. Directs regulatory activities, providing strategic direction, and definition. Manages to ensure all regulatory activities for development and marketed products are achieve...
We are looking for a Trials Safety Surveillance Manager either as a salaried employee with fully paid benefits, vacation or as an hourly employee. Responsible for • Identifying and assisting in the management of safety concerns within trials • Assisting Medical Affairs trials teams in implementing, executing and concluding trials • Assisting lead safety MDs in their evaluation of products’ safety...
Summary: The Application Specialist assists in the application of a newly developed technology as it relates to the industrial testing market. The newly developed technology will be applied to the food, veterinary and environmental testing market. The Application Specialist will assist the Manager, Applications and other team members to conduct small scale experiments in the newly constructed labo...
Job Description Manage projects/engagements delivering sales, marketing and managed markets solutions. Familiarity with the application of analytics to sales and marketing problems such as: Commercial model design, Sales Force Sizing, Territory Alignment, Sales Call Planning, Incentive Compensation Market segmentation, marketing program ROI, marketing mix optimization Managed markets pull through...
Job Description Conduct simple and advanced data analyses to help clients make good business decisions Assist in the development of analytic data marts. Apply advanced statistical, econometric and optimization models and algorithms to real-world business problems. Develop new statistical models as well as provide analysis using existing models. Develop and maintain skills to the highest standards...
Job Description Manage projects/engagements delivering sales, marketing and managed markets solutions to Pharmaceutical clients as well as clients from other Industry verticals such as Retail, Financial Services, Supply Chain etc. Function as trusted delivery leader for key Axtria client engagements. Make presentations and recommendations to clients such as marketing, sales and operations executiv...
Hello, Please do let me know if you are available for the below position. Job Title: Labware LIMS Developer Location: New Brunswick, NJ Duration: Long Term Job description: Must have significant experience and demonstrated proficiency in the support, maintenance and use of large or complex systems. LabWare LIMS v6 (and v5) experience highly desirable. Experience with laboratory instrument systems,...
Seeking extensive clinical development experience to help guide discovery strategies and focus pre-clinical resources and efforts most effectively for big pharma research & development activities. Must be a strategic expert and savvy diplomat to work closely with global pharma CEO in the analysis, selection and internal promotion of drug development strategies from evidence-based medicine to susta...
Establish and manage and an effective and knowledgeable quality and compliance organization, with specialization in providing quality oversight for commissioning, qualification, and validation of GMP facilities, utilities, equipment, instruments and computer systems used in the manufacture of clinical supplies. Additionally, lead and manage computerized systems compliance audits for applications a...
Position: Validation Specialist I Location: New Brunswick, NJ Job Description and Responsibilities: • Manage routine calibration, validation documentation and monitoring systems. • Generate and execute all Validation protocols (IQ/OQ/PQ) of all site equipment including production equipment, product storage, utilities (as applicable) and other related systems in an FDA regulated environment. • Asse...
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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: 2013.1.5.22-219 
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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: 2013.1.5.22-219