Biotech Jobs in Iselin, New Jersey

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166 Iselin, NJ Biotech jobs found on Monster.

Jobs 1 to 20 of 166
Senior Regulatory Manager Requirements: -Bachelor’s degree in science or health related field required; Advanced degree preferred (PhD, MD, PharmD, or equivalent) -6-8 years relevant pharmaceutical industry and regulatory experience -Documentum is a MUST; eCTD (electronic common technical documents) is a MUST -Biologics experience preferred but not necessary Responsibilities: -Develop a pro...
Our client is the world's leading chemical company. With more than 110,000 employees, six affiliate sites and approximately 380 additional production sites worldwide they serve customers and partners in almost all countries of the world. They combine economic success, social responsibility and environmental protection. Through science and innovation they enable customers in almost all industries t...
TechLaw, Inc., a nationwide Environmental Consulting firm, seeks chemists and biologists of all levels for Environmental Services Assistance Team contract supporting U.S. EPA laboratories located in Edison, NJ. Experience with organic and inorganic laboratory equipment, laboratory procedures, sample extractions, and EPA analytical methods are desired. Candidates must have at least a BA/BS degree...
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...
Accountabilities: The Auditor is accountable for review of data (submission/ pre-submission data that goes to FDA) critically per current in-house and compendia requirements to ensure completeness and accuracy of the data. There is heavy penalty for non-compliance of activities laid down in consent decree. · Depending upon submission (Annual review, ANDA, NDA, CBE, PAS, Response to FDA deficienc...
CorePharma LLC is a fast growing mid-size generic pharmaceutical company with approximately 250 employees, located in Middlesex, New Jersey. We are a fourteen year old firm principally in the business of developing, manufacturing, and distributing pharmaceutical products for the United States market. JOB SUMMARY: Under the direct supervision of the Supervisor, Quality Control Laboratory, the inc...
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...
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...
If you are interested in a GREAT contract opportunity to get your foot in the door with a top chemical company in the world please email a word .doc version of your resume to *****. This is an entry level role (No MS or PHDs will be considered) The successful candidate will perform a variety of routine chemical and physical tests for the Analytical Services and Materials Charact...
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...
Responsibilities: • Prepare and manage aggregate reports, EU Renewals and Risk Management Plans (RMPs) for investigational compounds, compounds in various stages of clinical development and marketed products, using the timeframes referenced in the project plan. • Circulates report for team review and quality control/quality assurance. • Update the document reconciling the reviewers'/auditors' c...
Must have: - PhD - 10 years of pharmaceutical experience. - Expertise in applying LC/MS, GC/MS, high resolution MS, and tandem MS for the characterization of organic compounds and degradation products. - Experience in operating and maintaining LC-MS/MS. - Experience in LC-MS/MS method development and optimization, validation, data analysis, and sample preparation techniques. - Expertise in m...
Joulé Scientific Staffing has an opening for a contract Analytical Chemist at a major pharmaceutical company in the Clark area. Requirements: MS in Chemistry 2-5yrs of experience Experience with routine HPLC and MS operation, HPLC method development, maintaining equipment operations, mobile phase and sample preparations, and preparing samples and methods for routine screening and analysis. Re...
Hays Life Sciences has partnered with a prominent global pharmaceutical client seeking a candidate who will be responsible for the development of formulations for topical products. Our client specializes in generic products for topical and oral administration. This person will need experience working with semisolid and liquid dosage forms. Additionally, this candidate will also be responsible for ...
Seeking a Product Development Manager with direct experience working with Semi-Solid, Solid and Liquid formulations. The purpose of this position is to direct the development of formulations and manufacturing processes of new products, including but not limited to the general oversight of all issues associated with guiding the development process from pre-formulations work to the manufacture of th...
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...
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...
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...
Eurofins is the world leader in the food, bio/pharmaceutical product testing. It is also number one in the field of environmental laboratory services and one of the global market leaders in agroscience, genomics, discovery pharmacology, and central laboratory services. With over $1 billion in annual revenues and 13,000 employees across 170 sites in 35 countries, Eurofins is a leading international...
Company Confidential Berkeley Heights, NJ, 07922
We are eagerly reviewing new resumes and have 2 openings for Clinical SAS Programmers. Requirements: -Bachelor’s degree or higher in analytical field -At least five years of progressive SAS experience within a pharmaceutical setting. -Good knowledge of statistical terminology, clinical data structure , clinical tests, medical terminology, regulatory standards and protocol designs. -Strong SAS...

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