Biotech Jobs in New Jersey

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304 New Jersey Biotech jobs found on Monster.

Jobs 1 to 20 of 304
Please note this is a 5 months contract position Skills: Microbiology experience, GxP Documentation, Excel Description The individual will perform research studies utilizing standard and modified methods in-vitro such as microbial kill time and minimum inhibitory concentration. Clinical studies will require cup-scrub sampling to collect facial skin bacterial samples from human subjects, processing...
Worldwide Clinical Trials (WCT) is a leading therapeutically focused Contract Research Organization (CRO) that applies deep therapeutic expertise to help customers achieve their drug development goals. WCT’s global footprint, full complement of development service offerings, and innovative use of proprietary and cutting edge technology, bring about an environment which allows us to focus on identi...
Senior Medical Writer - Biotech Company seeks a Senior Medical Writer to prepare clinical documents under strict timelines to support drug development at their Bridgewater, NJ facility. This is a full-time position, where you will earn a highly competitive salary, based upon your experience. You will also receive a full benefits package and the potential to earn a discretionary annual bonus for ex...
Overview: Celldex Therapeutics seeks an experienced professional to join our company as Drug Safety / Pharmacovigilance Specialist. Potential candidates who can commute to our Hampton, NJ office are strongly preferred. For those who can commute to our Needham, MA or Branford, CT offices, periodic travel to the Hampton office will be required. Position Responsibilities: The Drug Safety / Pharmacovi...
Molecular Pharmacology Job Description We are a Neuroscience company in the contract research space that focuses on many projects ranging from neurodegenerative diseases to psychiatric disorders. Our in vitro molecular pharmacology group is looking for a well-rounded molecular biologist and/or molecular pharmacologist possessing a MS or BA, and should have at least 2 to 5 years of experience in a...
Senior Regulatory Affairs Manager (CMC) Perm Job Will Relocate! Our client a global pharmaceutical organization is seeking a Senior Regulatory Affairs CMC Manager to join their team. This is an exciting time to join this organization since they are in an expanding phase offering tremendous growth opportunity. This opportunity is located in the Northern NJ area, Relo is offered for the right candid...
Clinical-Scientific - Pharmacology Associate CANDIDATES MUST HAVE Argus experience Duration: one (1) year in length Job Description: Enter applicable information into the global safety database for initial or follow up cases received via paper, fax or email. Book-in, quality check and initially assess cases from suppliers sending cases to DSS via paper, email or fax. Accept E2B cases received thro...
Please note this is a 1 year contract position. Client is looking for those with Device experience and Pharma prior work experiences. Skills: Clinical Research Associate experience, Clinical Monitoring, Medical Terminology Candidates should be able to Travel. Prepare and independently performs study site qualification, initiation, interim monitoring, and close-out visits at the clinical investigat...
Director, Supply Chain Management & Planning: Innovative Mid-size Pharma, Morris County, NJ Summary: Our client is a stable and growing mid-size pharmaceutical company with marketed drugs and multiple expected product launches in the near future. They have a newly created position open and they are seeking to hire a sharp, experienced, and passionate supply chain professional. In this role you wil...
Qualifications: Minimum of a BS degree Regulatory experience preferred Pharmaceutical/Biological manufacturing or Quality experience preferred Experience preparing CMC (Chemistry, Manufacturing, Controls) post approval submissions preferred Experience with Trackwise and regulatory tracking databases preferred Proactive and highly productive Sound judgment Attention to detail Strong written and ver...
CMC Regulatory Affairs Associate Princeton, NJ Our client, a global pharmaceutical organization is seeking a Regulatory Affairs Associate, CMC to join their team. This is an exciting time to join this organization as they recently brought several new products to market. Position offers career growth and a rewarding working environment. This is a temp to perm position, with strong compensation! Pos...
This is Energizer Holdings, Inc. With 30 brands and over 14,000 people in 50 countries all over the world, Energizer simplifies and enhances the lives of our consumers all over the world. But the challenger spirit that unites us adds up to even more than the sum of our parts. In fact, we're made up of 30 established consumer brands the world over, from Schick® and Wilkinson Sword® shaving systems...
TAKE Life Sciences are domain experts in the areas of Clinical, Regulatory, Safety and Compliance and are motivated by the success of our clients. We pride ourselves on our industry insight, our simplification approach and our pragmatic solutions which improve outcomes, ensure compliance and enable growth. Our capabilities cover strategic and change management consulting, technology and BPO. The U...
Responsibilities Summarize, analyze & interpret test results in preparation for submission to regulatory agencies. Review and approve or modify protocols and study proposals for contract laboratories Ensure all tests performed for regulatory submission meet Good Laboratory Procedure requirements Support R&D development and operations teams for determination of test requirements, sample preparation...
Job Descriptions: Ortho Clinical Diagnostics, Incorporated, a $1.9B global company, is recruiting for a senior global HR business partner role to be located in Raritan, NJ. Ortho Clinical Diagnostics Incorporated (OCD) provides high-qualityin vitromedical testing products that help people recover and maintain health throughout the world. Our vision isenabling people to be healthier feel better and...
Ortho Clinical Diagnostics, Incorporated, a $1.9B global company, is recruiting for a Customer Business Manager to be located in Utah/Nevada area. Ortho Clinical Diagnostics (OCD) provides high-qualityin vitromedical testing products that help people recover and maintain health throughout the world. Our vision isenabling people to be healthier feel better and live longer. Our products include reag...
Job Title: Lab Technician Position Description Able to execute and analyze molecular and ELISA based assays according to detailed protocols. Able to show thorough documentation of all work. Assignments are task-oriented with detailed instructions and work is closely supervised. Position Requirements Bachelor's degree in Science-related field. 1+ years ELISA experience. 1-2 years industry laborator...
TechData is hiring SAS Programmer, Biostatistician, Clinical Data Manager, Clinical Research Scientist/Clinical Study Manager for our pharmaceutical clients in Northern NJ. Please see below requirements and send your resume to: *****. TechData is a leading provider for temporary and permanent positions in the pharmaceutical industry. TechData offers very competitive pay ra...
ASSOCIATE DIRECTOR WITH ONCOLOGY REQUIREMENT #14-00716 RECRUITER: MICHELLE ASHEN JOB LOCATION: LAWRENCEVILLE, NJ JULY 16, 2014 Project Description: The Associate Director will be a PhD or PharmD with at least 3-5 years of relevant experience or M.S. greater than 5 years of relevant experience in the Pharmaceutical Industry A background in Medical Affairs or Clinical Development and specialty exper...
Johnson & Johnson companies are equal opportunity employers. Associate Director, Central Monitoring-00000ONA Description Janssen Research & Development, LLC, is recruiting for an Associate Director, Central Monitoring, to be located in Raritan NJ, Titusville NJ or Spring House, PA or Belgium/Netherlands. Janssen Research & Development, L.L.C. develops treatments that improve the health and lifesty...
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