R & D Jobs in Cranbury, New Jersey

108 jobs

At Joulé, you could say the right match is in our DNA. We're the specialists in Scientific Staffing. Our unmatched industry network and geographic reach enable us to place professionals like you at top firms every day. For more than 20 years, we've been providing temporary, contract and direct staff to pharmaceutical, biotechnology, food, flavor and fragrance, specialty chemical and other scientif...

This is a physician position in a mid-size diagnostic pharmaceutical and medical device company, with a broad range of medically-oriented responsibilities and activities in (1) supporting the sales force in its efforts to sell contrast media, imaging solutions, and medical devices, (2) supporting Professional Services in answering customers’ medical queries, and (3) in the modalities of contrast-e...

Leading Diagnostics Company seeks a Medical Communications Manager for a permanent opportunity. Great Benefits!! The incumbent is responsible for managing global Medical Communications and Medical Education activities. ESSENTIAL DUTIES AND RESPONSIBILITIES * Plan medical communication and education activities with Medical and Marketing * Prepare and edit abstracts and posters for congress pre...

Leading diagnostics client seeks an Associate Director, Drug Safety Medical Evaluation, Drug Safety Physician for a permanent opportunity. -15-20% Domestic and international travel maybe required. Must work on site ¿ Provides medical review and evaluation of safety information and adverse event reports for both marketed and investigational medicinal products and medical devices. Performs scient...

Manger through Director level, CMC Regulatory Affairs positions available. Multiple PERM opportunities with reputable pharmaceutical companies throughout New Jersey and Maryland. CMC Regulatory Affairs (Manager/Director) will provide regulatory leadership and oversight to for both pre- and post-approval roles. Emphasis will be primarily on biologics products, so large molecule experience needed. ...

Head of Formulation Development Kelly Scientific has partnered with an esteem specialty generic pharmaceutical company in Central NJ This position is responsible for independently creating and implementing formulation development strategies. The Formulation head within team based structure and provides direction for the progress of team projects. Serves as an SME (subject matter expert) in dealin...

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DOCUMENT MANAGER CLINICAL OPERATIONS Establish Pharmaceutical Company located in Princeton, NJ area has an IMMEDIATE NEED for Document Manager in Clinical Ops. This Contractor position involves managing the CTMF document process and guide Regulatory compliance with GCPs, ICH, and TMF. Will require high level of knowledge in Clinical Operations and GCP. Excellent Opportunity to take a leadership...

CLINICAL MANAGER FOR NAMED PATIENT PROTOCOLS REQUIREMENT #15-00657 RECRUITER: BRIDGET BURNS JOB LOCATION: PLAINSBORO, NJ MAY 26, 2015 Project Description: Demonstrates a strong operational understanding of conducting clinical trials Coordinates or contributes to key clinical documents (e.g. Protocols, ICF, DSUR/PBRER/RMP Reports) Establishes and maintains effective dialogue with Sponsor-In...

BUSINESS OPERATIONS ANALYST FOR MEDICAL DATA OPERATIONS REQUIREMENT #15-00553 RECRUITER: CHERYL AMBROSE JOB LOCATION: PLAINSBORO, NJ MAY 6, 2015 Qualifications: B.A/B.S. and a minimum of 2 years of equivalent relevant work experience. Experience in a pharmaceutical setting preferred Must be self-directed, capable of making independent decisions and must possess effective verbal and written ...

PROJECT MANAGER WITH CLINICAL, OUTSOURCING AND GLOBAL PROCUREMENT REQUIREMENT #15-00268 RECRUITER: BRIDGET BURNS JOB LOCATION: PLAINSBORO, NJ MAY 18, 2015 Project Description: · Drives the successful and timely execution and completion of the global tasks for Late Phase studies in adherence to Good Clinical Practices (GCPs), appropriate Standard Operating Procedures (SOPs), Food and Drug Adm...

CLINICAL PROTOCOL MANAGER FOR POST – PRODUCT APPROVAL STUDIES REQUIREMENT #15-00269 RECRUITER: BRIDGET BURNS JOB LOCATION: PLAINSBORO, NJ MAY 18, 2015 Project Description: Strong, late-phase global-operational experience in the management of post product approval pharmaceutical research (phases IV, REMS, RMP, PASS) Drives the successful and timely execution of global Post Authorization Safe...

Primary Duties and Responsibilities: · Responsible for planning, scheduling, execution and leading validation project assignments in coordination with the IT Manager and in accordance with Good Laboratory Practices (GLPs) and FDA 21 CFR Part 11. · Validation assignments include validation, qualification, and implementation of new and existing, processes, equipment, software, and instrumentation ...

Kelly Scientific is seeking a Quality Assurance Lab Technician with strong Lab experience and excellent GLP knowledge. The incumbent must will perform a variety of tasks in the lab and all in conjunction with GLP standards. Experience / Training / Education: Bachelor’s degree in Biology, Chemistry, or science related field. At least 2 years of experience in QA or QC, with focus on bio-analytica...

Company Confidential
Overview 1. Responsible for testing and release of finished products, stability samples, raw materials, registration, clinical and marketed products batches under GMP/GLP environment as per company's standard operating procedures and USP/FDA guidelines. 2. Performs analytical method validation according to an approved method validation protocol and support analytical method transfer activity as ...

Responsibilities will include: Perform Microbiological Assays Microorganism Identification Media Preparation/Growth Promotion Some weekend hours Minimum requirements: Ability to work independently Strong analytical skills Working knowledge of pharmaceutical microbiology & GMP’s 2+ years microbiology laboratory experience Bachelor’s degree in biology or related field Strong organizationa...

CHEMIST (Multiple Opportunities) Keywords: entry-level, chemistry, chemists, scientist, lab tech, lab technician, science, biology WILL TRAIN ENTRY LEVEL CANDIDATES! Accutest Laboratories is a nationwide environmental testing laboratory that has successfully delivered defensible data for over 50 years. Founded in 1956, Accutest is the nation’s 3rd largest environmental testing laboratory combin...

Clinical Document Manager Requirements: Bachelors Degree Minimum of 6 years in the pharmaceutical, biotechnology or medical device industry with at least 3 years experience in Clinical Trial Master File management Experience in GCP Quality Assurance is preferred Demonstrates thorough knowledge and understanding of regulatory authorities, GCPs, ICH guidelines and regulatory requirements for TM...

Joule has an opening for a contract Quality Analyst at an immunotherapy company in Plainsboro area. Responsibilities: Conducts qualitative and quantitative assessments to monitor product and process quality. Reviews and tests components, raw materials and finished products to ensure that such items meet company quality and safety standards. Prepares documents that report the results of laborat...

Joule has an opening for a contract Quality Control Chemist at a biopharmaceutical company in the Plainsboro area. Responsibilities: The major purpose of this position is the performance and reporting of analytical testing for product release. In addition, this position participates in testing activities related to failure investigation, method improvements, method validation and instrument qual...

Bracco Diagnostics Inc. is a subsidiary of Bracco Imaging which is part of the overall Bracco Group. The Company specializes in the clinical development, marketing and sales of diagnostic contrast imaging agents. Bracco Diagnostics Inc. primarily markets its products to hospitals throughout the United States. Bracco Diagnostics Inc. is committed to the discovery, development, manufacturing and mar...