Biotech Jobs in New Jersey

275 jobs

SEA GIRT, 08750
As a Water Treatment Specialist in the Army National Guard, you will make sure your fellow Soldiers have clean water and live and work in sanitary conditions. Water Treatment Specialists are part of the Army National Guard's environmental health and safety team, using their acquired knowledge and skills to fulfill several vital needs. These skills include site reconnaissance and preparation for wa...

SOMERSET, 08873
As an Army National Guard Chemical Operations Specialist, you'll be there and prepared whenever a community is flooded, an earthquake shakes the foundations of a city, a hurricane makes landfall, or an enemy uses biological or chemical warfare. You will know what to do to evacuate the area, control the situation, and solve the problem. In order to perform these functions, you will be trained to ex...

GENERAL PURPOSE OF JOB: Performs various types of microbiological testing under minimal or no supervision. Evaluates, records, reports data. Provides training and support for less experienced members of the lab. Assists Lab management in trending and reporting data, and in investigations. ESSENTIAL DUTIES AND RESPONSIBILITIES: A Listing of the job's essential or most important functions and respon...

Our client is a reputable pharmaceutical company seeking RNs with 2+ years of drug safety experience from a CRO or pharma company. Please see below and if qualified, please apply ASAP to receive a call from a recruiter with more information! This is a 6 month contract position extendable up to 4 years. Requirements: - Registered Nurse or Higher Degree in Health Care - Two years of experience in ph...

BIOLOGICS PROCESS OPERATOR REQUIREMENT #15-00705 RECRUITER: JESSICA CLARK JOB LOCATION: HOPEWELL, NJ JUNE 1, 2105 Project Description: · Operates control systems and processes in Biotechnology Pilot Plants as assigned · Prepares process buffers and reagents · Cleans equipment and maintain area in clean and orderly fashion · Recognizes and reports safety, maintenance and operational variances to ar...

SCIENTIST WITH EXPERIENCE IN CHEMICAL AND PHYSICAL PROPERTIES OF MATERIALS REQUIREMENT #15-00704 RECRUITER: DIANA WRIGHT JOB LOCATION: BLOOMSBURY, NJ JUNE 1, 2015 Project Description: Research and study the structures and chemical properties of various materials to develop new products or enhance existing ones. Usual requirement is a minimum of a bachelor's degree in science or a closely related f...

At Dr. Reddy’s, a global pharmaceutical company, you will contribute to making the breakthroughs of tomorrow a reality today! From making medicines more affordable to discovering innovative treatment options to satisfy unmet medical needs, we are dedicated to helping people lead longer and healthier lives. We are seeking dynamic and energetic individuals ready to inspire, ready to make a differenc...

CyberCoders Matching Great People with Great Companies Learn more about CyberCoders Regulatory Affairs EU Specialist Princeton, NJ Full-Time $120,000 - $130,000 Apply Apply Regulatory Affairs EU Specialist Princeton, NJ Full-Time $120,000 - $130,000 Apply Job Details We have an outstanding career opportunity for a Regulatory Affairs Specialist or Regulatory Affairs Subject Matter Expert (SME) with...

Job ID: 37985 Position Description: Clean Harbors is the leading provider of environmental, energy and industrial services throughout North America. The Company serves a diverse customer base, including a majority of the Fortune 500 companies, thousands of smaller private entities and numerous federal, state, provincial and local governmental agencies. Through its Safety-Kleen subsidiary, Clean Ha...

SCIENTIST WITH PEPTIDE SYNTHESIS EXPERIENCE REQUIREMENT #15-00703 RECRUITER: TROY SANDERS JOB LOCATION: LAWRENCEVILLE, NJ JUNE 1, 2015 Project Description: The successful candidate will become a significant contributor to a 6-month project related to the synthesis and purification of small peptides. The project will evaluate the final synthetic steps of peptide preparation, possibly involving soli...

MEDICAL INFORMATION MANAGER REQUIREMENT #15-00701 RECRUITER: MICHELLE ASHEN JOB LOCATION: PLAINSBORO, NJ JUNE 1, 2015 Project Description: Participate in ongoing comprehensive product/disease area training to serve as Medical Information expert within area of responsibility Ability to communicate on professional level with physicians, nurses, pharmacists, and other professional staff when discussi...

Join a winning team! The time is right to join our company! Joule Clinical and Scientific Staffing Solutions a System One division is looking to expand its dynamic internal team of recruiting and operations professionals. This position offers attractive earnings potential including a base salary plus monthly commissions and bonuses. In addition, we offer a strong benefits package and opportunity f...

Position Details: Position: Regulatory Submission Specialist / Dossier Associate Location: Pennington , New Jersey 08534 Duration: 12+ Months Contract Job Description: This dossier associate role will be to support the creation, distribution and archival of Regulatory submissions for Mature Products. These submissions are required to be in paper or NeES (non-eCTD Electronic Submission) format. Thi...

TRIAGE ASSOCIATE REQUIREMENT #15-00695 RECRUITER: CINDI PISNOY JOB LOCATION: HOPEWELL, NJ JUNE 1, 2015 Major Skills Required: Mastery of health / life sciences gained through either formal education or on job experiences. Mastery of AE processing both internally and externally, as well as the ability to understand the future impact. Mastery of the intricacies of CARES (the client’s drug safety dat...

Project Manager / Principal Investigator Openings in NJ and Utah Requirements: The major duties and responsibilities include the following: 1. Managing bioanalytical projects which includes: 1.1. Maintaining project schedule information (sample receipt, analyses required, data and report timelines, etc.) 1.2. Ensuring client contract and technical specifications are met. 1.3. Performing duties of...

Lead 6 or more Group Medical Directors responsible for multiple Clinical Development programs, provide strategic product development plans, medical and scientific expertise and strong knowledge of regulatory compliance requirements. Requirements: * Medical Doctorate or Doctorate of Osteopathic Medicine. * 10+ years experience in clinical trial activities, academic research or medical affairs. * Pr...

Mondelēz International is a whole new company that has been reimagined with a single focus in mind: create delicious moments of joy by sharing the world’s favorite brands. Launched on Oct. 1, 2012, and employing around 100,000 people around the world, Mondelēz International comprises the global snacking and food brands of the former Kraft Foods Inc. While Mondelēz International is new, our brands...

As mentioned there is still 2 positions here with this Global Pharmaceutical for their Oncology team. This project not only is going to be long term, but it is truly is going to be great experience in one of the hottest therapeutic areas in the industry with one of the top Oncology teams) 2 Opening's Title: Senior Principal Clinical SAS Programmer Duration: 18 months (Extendable) Authorization: No...

Perform both leadership and technical functions relating to leading the execution of specific Biostatistics and Programming project work and team members in a Phase I-IV clinical trial setting. Independently provide oversight of all statistical aspects in the design and analysis of clinical trials, including: 1. Contribute to efficient study design, preparing statistical consideration sections and...

DOSSIER ASSOCIATE FOR PAPER REGULATORY SUBMISSIONS REQUIREMENT #15-00693 RECRUITER: MICHELLE ASHEN JOB LOCATION: HOPEWELL, NJ JUNE 1, 2015 Project Description: This dossier associate role will be to support the creation, distribution and archival of Regulatory submissions for Mature Products. These submissions are required to be in paper or NeES (non-eCTD Electronic Submission) format. This resour...