Biotech Jobs in New Brunswick, New Jersey

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201 New Brunswick, NJ Biotech jobs found on Monster.

Jobs 1 to 20 of 201
Company Confidential New Brunswick, NJ
Director of Toxicology with Pesticides Please note that the Job is in Maryland Seeking Ph.D. level Director with 10+ years experience working in mammalian toxicology, pharmacology, developmental reproductive (DART) and/or related fields either in CRO, Pharmaceutical or AG Chem industries. EPA/AG Chem / Pesticides experience required. Doctoral degree and DABT certification required. Must have stron...
Business Development Director for GLP Lab selling Large Molecule studies Remote position, ideally on East Coast Qualifications: Bachelors Degree in Life or Physical Sciences. Masters or MBA preferred At least 5 years selling experience in pharmaceutical or biotechnology markets, preferably CRO services including testing to support the development of biologics and vaccines Thorough knowledge of dru...
This is a Permanent Position. Our client is looking for a candidate who will supervise a team of 10 chemist in addition, but not limited to, scheduling testing of raw materials, in process materials and finished products. ESSENTIAL DUTIES: · Supervise Quality Control team and compliance activities to achieve key site and corporate objectives. · Develops testing schedule for raw materials based on...
This position contributes significantly to the successful timely development of new pharmaceutical products utilizing analytical technologies to support customers in their formulation development activities. SPECIFIC DUTIES, ACTIVITIES AND RESPONSIBILITIES INCLUDE BUT ARE NOT LIMITED TO: • Works on problems of diverse scope where analysis of data requires in-depth evaluation of identifiable factor...
We have been retained by one of the world's leading manufacturers of medical/surgical disposable products to assist them as they expand their sales organization. You will be responsible to manage your own C. New Jersey Territory for their existing business and develop new sales primarily in the acute care market. With products that are clinically superior, you will call on various departments of t...
Fast growing, Life Sciences SaaS company seeks energetic and enthusiastic Business Analyst. If you are a Business Analyst with great interpersonal skills and a desire to learn while supporting our top selling software solution you may be the right candidate to join our growing team. As a Business Analyst, you must represent our company well by being professional, responsible and motivated to go ab...
Our Global Client is a large manufacturing company and they are looking for some talented QC Chemists to provide the following: ANDA ,Chemists, QC Chemists, Formulation Chemists, all kinds of Chemists needed. Great benefits. Perform various QC analyses on lab samples at mfg plants; Ensure compliance to cGMP’s and Safety & Health Programs. Analyze lab samples (raw material, in-process, finished pro...
*Experience in sterile injectables is required Roles and Responsibilities: Compile ANDA/NDA dossiers, including: requesting necessary documents from CMO/CRO, performing pdf CRO conversion and size reduction, bookmarking, and compiling Modules. Ensure quality submission. Manage regulatory document submissions, including: uploading all modules to eCTD software, performing hyperlinking, submitting th...
Director Epidemiology Job Summary: We are currently seeking a Director, Epidemiology in northern NJ location. This position, focused on clinical drug safety, provides support in epidemiology, signal detection and data mining, and risk management expertise to teams that are developing new medicines or marketing innovative products to patients. Responsibilities: Working as the epidemiology expert fo...
As a Sr. Research Investigator in Stability you will contribute to establishing the stability study strategy for drug substances/drug products for assigned projects and guides teams on this strategy. Position is responsible for the design and authoring of stability protocols for large molecules and writing stability sections for Biologic Licensing Associations (BLA), using scientific and technical...
Due Diligence for Health Care Business Integrity Program Department: Worldwide Transportation Reports to: Director of Global Trade Compliance Location: Piscataway, NJ; meetings possible in various NJ locations Qualifications project management; communications and organizational skills Education: BA Experience: at least 5 years project management; transportation and regulatory compliance knowledge;...
TRG has recently been engaged by one of our top clients located in New Jersey, a rapidly growing and respected Pharmaceutical organization that is actively seeking qualified candidates for the role of DIRECTOR/SENIOR DIRECTOR OF REGULATORY AFFAIRS to help them with the development of their cutting edge portfolio of pharmaceuticals. ADVANTAGES OF THIS OPPORTUNITY: CHANCE TO MAKE A DIFFERENCE – As t...
Email resumes to ***** or call me at 732 429 1850 asap Direct Client -Generic Pharma Client Location- Piscataway,NJ Fulltime/Permanent Role Salary-$ 150k Experience: -At least 10-15 years experience in filing IND’s, 505b(2) and ANDA’s for injectable, ophthalmics and solid dosage forms -Assembling documents for eCTD filing -Compiling eCTD filings using appropriate software -interact...
US-NJ-Validation Chemist – Instrumentation Services Distek, Inc., a rapidly growing leader in the scientific instrumentation field is currently seeking a Validation Chemist in the New Jersey area to perform Instrumentation Services at customer sites. The position will be responsible for on-site laboratory instrument: · Validation · Calibration · Testing · Installation · Repair The qualified candid...
Company Confidential North Brunswick, NJ, 08902
We are a fast-growing consumer product company with 2 locations in New Jersey and over 30 years of experience in the personal care/OTC industry. We have an immediate need to hire a Quality Control Manager. A successful candidate will have the ability to work in a fast-paced, team-oriented environment and must be able to multi-task effectively. A Bachelor’s Degree or higher in the Sciences is requi...
Must have: Strong Phase III regulatory writing experience AND PK/PD Phase I writing experience Therapeutic area experience in: oncology and/or endocrinology Duties and Responsibilities % of Time Provide medical writing support for development programs by hands-on writing of protocols, IBs, and CSRs. Participate in appropriate development teams and internal strategy and operations meetings. 60% Man...
Seeking an experienced company's Rave study builder who can work at our Edison, NJ location. Key Responsibilities: • Advise external customers and internal staff on best practices for implementing Company's software • Work with Project Managers in translation of customer needs in terms of system functionality to ensure a match between needs and actual system capabilities/limitations • Work directl...
Location: Piscataway, NJ Job Description: The role of Inside Sales Manager (ISM), is to drive and support sales efforts in a given territory - US by implementing the sales/marketing product and service strategies. The ISM will use his/her knowledge of the business and corporate contacts to commit to and deliver profitable initiatives that build sales. Responsibilities: The ISM will be responsible...
Medical Director, US Medical Affairs: Top 20 Oncology Drug to Treat Multiple Tumors Summary: You will be the US Lead MD/Physician for a Top 20 Oncology drug that treats multiple tumors/cancers as a mono and combination therapy. This is a very visible and challenging position with a Top Global Pharmaceutical/Biotechnology Company that has multiple top 20 drugs to treat solid tumors and blood cancer...
-Essential: • Minimum of BSc or Higher within a Pharmaceutical, Pharmacy or Chemistry discipline. • Extensive senior level technical experience within pharmaceutical analytical development, especially method development from scratch • Solid team management experience, particularly within appraisal, development and coaching of team members • Thorough understanding of pharmaceutical development regu...
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