Biotech Jobs in New Jersey

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763 New Jersey Biotech jobs found on Monster.

Jobs 1 to 20 of 763
Description Ortho Clinical Diagnostics (OCD) is a leading provider ofin vitrodiagnostic products and services, offering accurate, timely, and cost-effective solutions for screening, diagnosing, monitoring and confirming diseases. The company has approximately 3,800 employees around the world serving the global clinical laboratory and transfusion medicine community, and is committed to providing c...
Ortho-Clinical Diagnostics, Inc. (OCD) is a leading provider ofin vitrodiagnostic products and services, offering accurate, timely, and cost-effective solutions for screening, diagnosing, monitoring and confirming diseases. The company has approximately 3,800 employees around the world serving the global clinical laboratory and transfusion medicine community, and is committed to providing customer...
Toxicologist, Preclinical Research Demonstrate the ability to work independently and efficiently in order to complete high quality Toxicology Risk Assessments quickly in order to meet aggressive timelines. Must be detail oriented. Participate on various project teams and communicate clearly and effectively to team members, as well as to others within the department. Demonstrate the ability to m...
We currently have an excellent opportunity for a Program Manager located at our Princeton, NJ office. The individual will lead the product engineering group as well as some product development projects from initiation through manufacture (launch). Responsibilities will include influencing and supporting Strategic Business Unit (SBU) decisions, resource allocation, budget tracking, process improv...
Johnson & Johnson companies are equal opportunity employers. Associate Director, Regulatory Program Management-1303140522 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, ...
Experienced Chemical Engineer for research in fragrance ingredient synthesis and large-scale commercial production. Bring in new technology and advance capabilities for competitive advantage in fragrance ingredients. Responsibility - Apply chemical engineering principles of reactor design, chemical kinetics, fluid mechanics, heat transfer, mass transfer, thermodynamics, and process simulation & ...
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...
Sr Medical Dir Immunology up to 250k base Immunology Medical Director up to 220k base all openings offer Benefits - Full Relocation Assistance Available - Possible for the ideal candidate Bonus Eligible - Yes Interview Travel Reimbursed - Yes Sr Medical Dir Immunology up to 250k base SUMMARY: The Medical Director represents a key role of all aspects related with Medical Affairs responsibil...
CLINICAL SPECIALIST MANAGER JOB RESPONSIBILITIES 1. Create/Manage a team of clinical specialists to become experts of Nuclear Cardiology and particularly in Cardiac PET, Lung and Endocrine disease Diagnostics 2. Create the process and manage the resources required for set-up and installation of the Rubidium Elution System (RbES) and Ruby-Fill™ generator and ensure proper troubleshooting procedu...
Johnson & Johnson companies are equal opportunity employers. Senior Analyst Incentive Compensation-2765140619 Description Janssen Pharmaceuticals, a member of the Johnson & Johnson Family of Companies, is recruiting for a Senior Analyst – Incentive Compensation to be located in Titusville, NJ. Janssen Pharmaceuticals, Inc., a pharmaceutical company of Johnson & Johnson, provides medicines for ...
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...
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...
To maintain and coordinate Quality Systems related documents namely deviation reports, change controls and product complaints for compliance with cGMP and company procedures with minimal supervision. To review and write cGMP procedures under supervision. To process changes in analytical methods, test specifications and batch records. To issue effective documents including procedures, forms, report...
Follows current GMP requirements and complies with company safety policies. Participates in repair and maintenance of lab equipment and laboratory housekeeping (disinfection and cleaning). Initiate, document, and perform microbiological analysis on received test samples (including raw materials, bulk, final product, stability, water) as per USP, in-house, or customer methods. Evaluates and record...
This pharmaceutical company is known as a human health care (hhc) company seeking innovative solutions in disease prevention, treatment and care for the health and well-being of people worldwide. They use their talents to explore new therapeutic approaches that help address two key goals: meeting the medical needs of patients and their families, and improving their quality of life. Job Descriptio...
Job Number: 422564 Data Entry Specialist EZIJP00001842 Skills: Entering data from existing spreadsheets or correspondences to another spreadsheet. Able to work with multiple spreadsheets at a time. Entering names, selecting from drop down menu in Excel, dates, etc. May import data to another file as well. Superior accuracy and attention to detail skills. Must be organized Proficient in MS...
Our Company We are a rapidly growing pharmaceutical manufacturer with strong lines in hospital and ophthalmic markets, and many new products in development and awaiting FDA approval. In anticipation of long-term, substantial growth, we offer challenging, attractive career opportunities. Akorn is an Equal Opportunity Employer. M/F/V/D. The Opportunity We are looking for a temporary Quality Contr...
Description Our Pharmaceutical client based in Bridgewater, NJ has an immediate need for a Manager for the Quality control Analyst Job Details Job Category Scientific Job Title Manager Standards Job Code Quality Control Analyst : Quality Control Analyst Duties Drive timely resolution to assigned audit findings, ensuring that implication of process changes is considered across all relevant p...
Global pharmaceutical company is seeking a Director or Vice President of Quality to join their team. We are looking for a forward thinking quality professional to maintain and build upon our quality approach to providing pharmaceuticals. The Director/Vice President is responsible for the site’s quality systems ensuring the connection with manufacturing processes and business to customer needs. Yo...
JUNIOR DOCUMENT PUBLISHER WITH SAP EXPERIENCE REQUIREMENT #14-00860 RECRUITER: NATALYA VOLKOV JOB LOCATION: NEW BRUNSWICK, NJ AUGUST 13, 2014 Project Description: Document publishers work with an integrated system of computer applications to manage, edit and publish documents for submission to health authorities around the world. The candidate should have excellent computer skills, including...

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