Biotech Jobs in Vineland, New Jersey

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Please note this is a 2+ months contract position Skills: Consumer Chemist, GMP/Lab experience, Validation Products Detailed Job Description: Provide technical support to TT staff in formulated products. This includes Technology transfer, lab, pre-pilot, trial and validation for new products. Provide technical assessment of TT Consumer projects against the Product/process specification. When...
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...
Johnson & Johnson companies are equal opportunity employers. Associate Director, Regulatory Program Management-5590140917 Description Janssen Research and Development, LLC, a member of Johnson & Johnson's Family of Companies, is recruiting for an Associate Director, Regulatory Program Management to be located in Raritan, NJ; Titusville, NJ; or Spring House, PA. Janssen Research & Development, ...
Johnson & Johnson companies are equal opportunity employers. Group Director, R&D, Applied Science and Technology-1218140731 Description Ethicon, a member of Johnson & Johnson's Family of Companies, is currently recruiting for a Group Director, R&D, Applied Science and Technology (AST) to be located in Somerville, New Jersey. The Ethicon business offers a broad range of products, platforms and ...
XenoBiotic Laboratories, Inc. (XBL), a GLP-regulated Pharmaceutical Development Contract Research Organization located in central NJ. Primary Duties and Responsibilities: · Under regular close supervision, individual performs routine laboratory techniques. · Receives specific instructions on assigned task and expected results. · Maintains research notebooks in a well-organized manner. All nece...
Responsibilities: XenoBiotic Laboratories, Inc. (XBL), a GLP-regulated Pharmaceutical Development Contract Research Organization located in central NJ, is seeking an experienced autoradiography research professional to lead the QWBA group to conduct studies as well as manage and participate in other preclinical ADME studies. The successful candidate will serve as a Study Director/Group Leader in...
2 openings follow AVP of Marketing reports to VP of Marketing. VP of Marketing reports to VP/Head of Commercial Strategy & Operations. AVP will manage 5 groups with 5 direct reports. VP has 8 direct reports + 5 that report to AVP. The entire team is about 34. Benefits - Full Relocation Assistance Available - Yes Bonus Eligible - Yes Interview Travel Reimbursed - Yes AVP Evidence Lead Diabete...
Company Confidential East Windsor, NJ, 08520
Overview Responsible for testing of raw materials, establishing impurity and degradation profiles for active bulk drug substance and release testing of drug product produced using Aprecia Pharmaceutical’s proprietary technology. Description of Duties Research, design and create, QC friendly new procedure to achieve cost effective quantitative test methods. Perform analytical method development...
Growing Pharmaceutical client in Central/Northern NJ area is looking to fill a temp-to-perm role for a Director, Quality Assurance/Auditing with large molecule, biologic experience. This job will have the following responsibilities: ·Manufacturing is done on-site, so client needs a hands-on leader to oversee QA and internal audit compliance. ·Primarily GMP, but some GLP and GCP oversight as wel...
Johnson & Johnson companies are equal opportunity employers. Head of Clinical Development-0462140723 Description Janssen Diagnostics, L.L.C., a member of Johnson & Johnson's Family of Companies, is recruiting for a Head of Clinical Development located in Raritan, NJ. The Head of Clinical Development will serve as the primary point of contact and resource for development activities of diagnosti...
TechData is looking for Biostatistician (some can be telecommuting), SAS Programmer/Statistical Programmer (Some can be telecommuting), Recruiter, Project manager, Quality Assurance, Database Administrator, Drug Safety Specialist, Clinical Data Managerfor our pharmaceutical clients in Central NJ. Please see below requirements and send your resume to: *****. TechData is a l...
Ortho-Clinical Diagnostics is recruiting for a Manager, Worldwide Commercial Enablement, which is part of our Commercial Operations, and can be located off or on site, Rochester or NJ would be preferred. Ortho Clinical Diagnostics (OCD) is a leading provider ofin vitrodiagnostic products and services, offering accurate, timely, and cost-effective solutions for screening, diagnosing, monitoring an...
Requisition ID 25178BR Title In-House Clinical Research Associate (CRA) Job Category Clinical Trial Management Job Description PURPOSE: Responsible for the support of assigned sites in accordance with Good Clinical Practice (GCP), ICH guidelines, federal regulations and SOPs. Close collaboration with other members within Clinical Trial Management (CTM) and with various representatives within C...
Job Number: 424074 SAS Programmer II OVERVIEW Provide statistical programming expertise in SAS for the production of analyses, tabulations, graphics, and listings from clinical trial data. Key responsibilities and skills include, but are not limited to, the following: Contribute to the preparation of analysis plans. Prepare, document and test required programs and procedure data displays in ...
Job Responsibilities - Define global CMC regulatory strategy for ANDA filing of injectable products and manage the preparation, assembly and review of the quality (CMC) sections of regulatory submissions. - Liase with FDA in written communications - Coordinate responses to global regulatory agencies dealing with quality sections of global regulatory submissions Qualifications - At least bache...
J. Knipper and Company’s continued growth as the Pharmaceutical industry’s leading sample services provider, creates long term career opportunities for high performing individuals with a strong desire to learn, succeed, and advance. One of those opportunities is now available in our premier Professional Services Department. With over 25 years of continued growth as one of the largest employers in...
IBA Molecular, a global leader in the radiopharmaceutical industry, is dedicated to delivering the best products, and services in the fields of personalized medicine, molecular imaging and nuclear medicine. With our corporate headquarters in Dulles, VA and locations throughout the US and Europe, IBA Molecular’s global presence serves customers throughout the world. With over thirty years of manufa...
PLEASE EMAIL RESUMES TO ***** Client- Pharma Location- South Plainfield, NJ Duration- 3 m contract to Hire Protein Chemistry background. MS/Ph.D. Not required. Below are some of the Duties and Responsibilities. Perform QC chemistry testing for research and clinical batches. Perform stability testing for research and clinical batches. Execute method validation activities in ...
One of the world’s leading chemical companies has a job opening in their central New Jersey location. The company seeks a research engineer with a degree in Chemistry or Chemical Engineering to work on experimentation related to catalysts that reduce harmful emission gases. The company designs and develops catalysts and adsorbents used to treat and purify emission gases from power plants, or from...
Johnson & Johnson companies are equal opportunity employers. Staff R&D Engineer-9583140428 Description Mentor, a member of Johnson & Johnson's Family of Companies is currently recruiting for a Staff R&D Engineer, to be located in Somerville, New Jersey. Mentor Worldwide L.L.C., is a trusted global leader in aesthetic medicine among both consumers and clinicians by providing a broad range of in...

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