R & D Jobs in Linden, New Jersey

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175 Linden, NJ R & D jobs found on Monster.

Jobs 1 to 20 of 175
· High school diploma or general education degree (GED) is required; and one year related experience in QA Inspection; or combination of education and experience. · Ability to read and comprehend simple instructions, short correspondence, and memos in English. · Ability to speak effectively in English in one on one or small groups. · Ability to add, subtract, multiply, and divide in all units o...
Senior Manager Regulatory Affairs Location: Iselin, NJ Duration: 6 months Requirements: -At least a Bachelor’s degree in Life Sciences (preferably a Master’s degree) -Minimum of 10 years general Regulatory industry experience, with the preponderance of experience being in the area of Regulatory advertising and promotion review. Responsibilities: Promotional material (75%): -Collaborate wit...
A leading provider of drug development and manufacturing services to pharmaceutical, biotech and medical device companies around the world is seeking a qualified Chemistry Data Reviewer. Qualified candidate will review raw data in support of GMP testing. Bachelor's degree with 2+ years of the following experience required: -Analytical Chemistry required. -GMP experience required. -Experience ...
Celgene is a global biopharmaceutical company leading the way in medical innovation to help patients live longer, better lives. Our purpose as a company is to discover and develop therapies that will change the course of human health. We value our passion for patients, quest for innovation, spirit of independence and love of challenge. With a presence in more than 70 countries - and growing - we l...
Our client – a growing company in central NJ, is looking for an executive level professional with extensive regulatory affairs experience in the pharmaceutical industry. Excellent salary + Bonus + relocation. Job Posting #: 1535 Job Title: Sr. Director – VP – Regulatory Affairs Overnight Travel: 5 % Location: Edison, NJ Relocation: YES – Sign on bonus to cover relocation expenses Compensatio...
Early Clinical Development Specialist - III Must have: - BS degree (will not consider non-degreed) - Direct clinical experience (e.g. nursing) or experience conducting Phase I clinical research in the pharmaceutical industry - Phase I experience with direct tasks of regulatory document authoring (protocols, clinical study reports, IND updates), project management/oversight for Phase I studies,...
Job Purpose: Maintains product quality by conducting microbiologic tests; communicating results. Duties: * Organizes work by confirming product specifications. * Maintains clean and safe work environment by maintaining aseptic methods and protocols; following standards and procedures; complying with legal regulations. * Prepares cultures by obtaining in-process and finished product samples. ...
Industry: Pharmaceutical Must have: - BS Life Sciences/Engineering - Experience supporting clinical trials/programs - Experience with Microsoft Project - Experience with Clinical Trial Management Systems such as Spectrum or Impact Responsibilities: · The Clinical Project Specialist will be responsible for supporting and managing the Early Stage Clinical Development functional area planning ...
Peak Environmental Inc. is looking to add staff members to our environmental consulting company to address our expanding workload in the areas of environmental site assessments, investigation and remediation. This is a unique opportunity for growth at any level. Entry level candidates will find a wide variety of interesting projects to participate in; mid level candidates will find increased proje...
Requirements: -Educated to degree level (biological science, pharmacy, or other health-related discipline preferred), equivalent nursing qualification or other equivalent experience (degree is not required) -Min 5 yrs experience within biotech/CRO or smaller company (can’t just have big pharma exp), would consider experience over degree but depends on background, (high exp working in house, they...
Responsible for the management of outsourced contract manufacturing organizations (CMOs) involved in the production of APIs and finished dosage forms for the Company during late-stage development and commercialization phases of product life-cycle. The project manager will have responsibility for tracking project contracts, budgets, timelines and deliverables. The project manager will also provide ...
Worldwide Clinical Trials is a therapeutically focused global CRO that provides full-service drug development services to the pharmaceutical and biotechnology industries. As one of the most innovative and scientifically-driven contract research organizations, we offer exceptionally strong clinical trial methodology integrated with an effective global operations network. We are currently seeking hi...
Company Confidential Summit, NJ, 07901
Exciting Data Management position with excellent potential. We are eagerly reviewing new resumes. Please submit if you feel qualified with the below skills. Responsibilities will include, but are not limited to: 1. Functional proficiencies: • Reviews synopsis/protocol and attends Synopsis Review Committee (SRC) meetings • Leads DM study start-up and maintenance activities - CRF design/edit che...
Admera Health is an advanced molecular diagnostics company focused on personalized medicine and non-invasive cancer testing. Our goal is fulfill unmet medical needs with cost-effective tests and accurate analysis to guide patient care by utilizing next generation sequencing technologies and advanced bioinformatics to redefine disease screening, diagnosis, treatment, monitoring, and management. It ...
Supervise and reports of overall product development activities to Sr.VP of R&D.Issues of meeting time line ,enhancement of personal step up activities. Analysis and resolutions for projects progression blocks of specifically of ANDA and generally other projects in lines of R&D layer out. Duties requirements encompasses solid dosage a must soft gel plus. Preformulation and as well as formulation...
AAIPharma Services is a leading provider of drug development and manufacturing services to pharmaceutical, biotech and medical device companies around the world. With over thirty years of drug development expertise, we offer exciting and challenging career opportunities in a dynamic and growth oriented business. Our facility is located in Edison, NJ, voted one of "America's Best Places to Live" by...
Company Confidential Edison, NJ
Open Ended contract hiring ASAP Local candidates only Qualified resumes will receive feedback within 24 hours Inorganic Chemistry: Instrumentation and analysis: ICP-Metals TPH, O&G TOC-Shimadzu COD TSS, TDS An Environmental Laboratory Analyst who has experience in wet chemistry. The candidate should be familiar with inorganic parameters. These tests include: TSS, TDS, Metals digestion, T...
Manage projects/engagements delivering health economics/outcomes research (HEOR) modeling and analytic solutions. Familiarity with the application of analytics to HEOR problems such as: • Cost-effectiveness model design, including Markov and discrete event simulation (DES) models. • Integration of data from multiple sources, such as clinical trials, claims databases, and literature. • Biostatis...
TechData is looking for Regulatory Specialist, Biostatistician (Some remote), SAS Programmer/Statistical Programmer (Some can be telecommuting), Clinical Research Scientist, Clinical Research Physician, Drug Safety Specialist, Safety Trial Manager, Medical Affairs Contract Manager/Outsourcing manager, Sr. Clinical Data Manager, for our pharmaceutical clients in Central NJ and Northern NJ. Please s...
Job Number: 423225 SAS Programmer Responsibilities will include, but are not limited to, the following: 1. Provide programming input to CRF, SAP, analysis file specifications, and tables, figures, and listings (TFLs) shells. 2. Write SAS programs to generate derived analysis datasets, perform analysis, and TFLs. 3. Perform ad hoc flexible and rapid programming arising from questions generated f...

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