R & D Jobs in Linden, New Jersey

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

Jobs 1 to 20 of 172
Clinical and Regulatory Analyst - III Must have: - Bachelor's degree, preferably in nursing, pharmacy or a biological science - At least three years of experience in a hospital, pharmaceutical, or research position. - Prior experience in coordinating and overseeing the production of Aggregate Reports (PSUR, DSUR, PAER etc.) and RMPs required. - PSUR authoring experience would be considered. ...
Company Confidential Edison, NJ, 08837
POSITION SUMMARY: The incumbent will manage all activities of the Quality function and have overall hands-on responsibility for the development, deployment, administration and maintenance of quality systems and product control internally and at Contract Organization encompassing Biologic and Radiologic development programs. ESSENTIAL DUTIES AND RESPONSIBILITIES: Responsibilities include, but ar...
Currently we have a temporary opening for a Facilities Engineer to support a company located in the Short Hills, NJ area.   Responsibilities: Manage major construction projects at multiple North American sites. Developing design concepts with the users and design engineering firm Developing request for proposals to bid projects, coordination with customers, contractors and consultants, Revie...
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...
Hays is currently recruiting for a Project Manager for our global pharmaceutical client located in Northern NJ. This hands-on, process driven Project Manager position is a 6 month contract job. This position is an excellent opportunity to leverage your Drug Development and Regulatory Filing experience in a tangible project-based setting. This position will be responsible for hands-on daily projec...
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,...
Medical Writer/Clinical - III Location: Rahway, NJ OR Upper Gwynedd, PA Must have: Education: Bachelor’s Degree required. RN degree, PhD in health related field and/or PharmD is a plus. Skills: • Must have at least 4 years of medical writing experience within the pharmaceutical industry and at least 2 years of this experience must have been spent authoring clinical documents for regulatory su...
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 ...
Responsibilities: · Support the MRL clinical monitors (physicians) who oversee the conduct of Phase I clinical trial. Various therapeutic areas (NON ONCOLOGY) · Lead a team of functional area members through the end-to-end process of PHASE I study conduct (normal healthy volunteer, PK/PD, DDI, ADME, special populations) · Order study related supplies Oversee CRO management for sourced Phase I t...
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...
Company Confidential Newark, NJ, 07101
Currently seeking dynamic sales entrepreneurs for a unique career opportunity in compounding pharmaceutical sales in the greater Newark area. Requirements · 5-7 years pharmaceutical sales experience · Established relationships with specialists in interventional pain management and/or: orthopedics, rheumatology, neurology, endocrinology, podiatry, oncology and primary care physicians. Preferenc...
Founded in 1977, Lipoid is a globally leading manufacturer of phospholipids for the pharmaceutical industry. Lipoid also distributes phospholipids and botanical extracts and botanical actives made by LIPOID-Kosmetik, a member of the Lipoid Group of Companies. Lipoid is headquartered in Europe and is privately held. Our high-grade products are scientifically developed in Lipoid’s laboratories and ...
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...
Kerlo Research Inc. is a privately held company based in Plainsboro, New Jersey and is a specialist provider of clinical research services. In collaboration with DM Clinical Research based in Houston, TX, we are looking for a reliable, dedicated and a motivated Clinical research coordinator. We have an urgent need to fill this position as we have ongoing studies with a good number of patients enr...
Job description JOB TITLE: Associate Manager, Biologics Development LOCATION: Edison, NJ JOB DESCRIPTION AND RESPONSIBILITIES: The successful candidate will be responsible for biologics processdevelopment by working with CMO for multiple development and technology projects, providing both technical oversight and strategic guidance in a fast-paced environment. Develops high-performing cell cult...
Job Description Responsibility: Responsible for the validation of stability-indicating analytical methods applicable to specific active pharmaceutical ingredients and pharmaceutical drug products Work Performed: • Perform methods development and validation using analytical techniques such as HPLC, GC, UV and FT-IR. for • API in drug substances • API, Preservatives and related degradation pro...
Responsibility: Responsible for the development and validation of In Vitro methods for Semi-solid pharmaceutical drug products. Work Performed: • Independently manage the development and validation of In Vitro methods for Semi-solid pharmaceutical drug products using Franz Cell • Technically supervise and coach junior chemists in validation and generation of IVRT data for Semi-solids • Perform...
GENEWIZ, Inc. is a leading global genomics service company. Excelling in both science and customer support, GENEWIZ is a trusted provider for DNA sequencing, gene synthesis, molecular biology, next generation sequencing, bioinformatics, and GLP regulatory services. Customers depend on GENEWIZ to achieve results in a rapid, cost-effective manner through specialized expertise and customizable, scala...

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