R & D Jobs in Franklin Lakes, New Jersey

79 jobs

Our client is a major medical device company and is seeking seasoned Regulatory Affairs professionals with either PHARMA OR MED DEVICE experience within RA. There are currently 2 openings and the manager is looking to fill these roles ASAP. If interested and qualified, please apply today to receive a call from a recruiter with more information! These are 6mo+ contract positions with possibility t...

POSITION PURPOSE The primary role of the Director, Product Development is to lead the execution of product development programs in support our growth strategies in patient care. Direct teams of scientists and technical professionals in the development of new formulations and products and provide scientific support to existing product lines. ESSENTIAL FUNCTIONS AND BASIC DUTIES Responsibilities ...

Everest Clinical Research ("Everest") is a contract research organization providing statistical, data management, statistical programming, medical writing, subject randomization and drug supply management, regulatory submission, and clinical trial management to pharmaceutical, biotechnology, and medical device companies. We serve some of the best-known companies worldwide, and work with many of t...

This is Edgewell The Edgewell Name Edge expresses our drive to always be on the leading edge of innovation, and to deliver meaningful advantages over competitive products. It also evokes the rich heritage of our largest global business: shaving, which is quite literally about putting an edge on blades. Well reflects our ultimate goal, as a Personal Care business, to deliver well-being for the peo...

Job Description: The R&D Systems Engineer works with other engineers and managers, within Engineering, Quality, and other functions, to identify opportunities for improvement and execute improvement initiatives. This includes but is not limited to identifying and executing improvements to Design Control documents, driving CAPAs to closure, and representing Product Development regarding PLM and CA...

Our client is a large medical device company - applicants should have LABEL REVIEW experience in a regulated environment. This person will be communicating with a diverse group so excellent communication skills is required! Requirements: 3+ years experience in pharmaceutical, medical device or other similar regulated environment Label review experience Demonstrated knowledge of RA/QA and FDA r...

Our client is a large Medical Device company hiring for a contract Data Steward to work in the Regulatory Affairs department. Applicants should have strong data mining and process analysis experience working in an FDA regulated environment and have experience working with Oracle. If interested, please apply today as this is an IMMEDIATE need! MUST HAVE: - Strong MS Office suite skills (Excel, Wo...

Responsibilities: · Programming of SAS analysis datasets from files exported out of EDC system (Velos, RedCap, and other EDC systems like Oracle Clinical, Rave, Inform, etc.). · Programming of clinical data outputs for quality reviews, exploratory data analysis, publications, and other reports. · Programming of tables, listings and figures (TLFs) for data safety monitoring committee and for int...

Currently we have a temporary opening for a Microbiologist to support a company located in the Mahwah, NJ area. Responsibilities: Performs routine laboratory functions including maintaining equipment, preparing lab materials and supporting experiments as needed. Accurately conduct specified tests, documents findings in a detailed manner and compiles data for reporting of results. Collect enviro...

Associate Clinical Specialist Requirements: BA in related field 3+ years’ experience in a Pharma/CRO/Medical Device company. Must have experience managing projects. Responsibilities: -Manage the day-to-day activities of one or more clinical studies, which may be either Investigational Device Exemption (IDE), post-approval, post-market surveillance, feasibility and/or marketing studies. -Ens...

Requirements: - BA/BS in Scientific discipline required. Engineering strongly preferred - 510(k), IDE, PMA (original/revision/supplements) preparation - Minimum 2 years’ experience in FDA regulated industry - Working knowledge of Medical Device Regulations (FDA required, international a plus) - Proficiency with MS Office required, strong MS Excel knowledge preferred Responsibilities: - Ensu...

Job Description : Contract position for a Regulatory Affairs Associate for medical devices. Work with international Regulatory Affairs (RA) affiliates regarding labeling changes. Initiate, review and approve labeling changes for RHQ change. Work with international RA affiliates to strategize on RA pathway in their respective markets. Participate on product development teams to ensure US and E...

Currently we have a temporary opening for a Research & Development Technician to support a company located in the Suffern, NY area. Responsibilities Assist formulation scientists with a broad range of research and development activities including execution of trial batches, physical testing of drug substances at different stages of development, and writing and updating SOPs Perform set-up, oper...

TechData is looking forBiostatistician (Some positions are remote), Statistical Programmer (Some positions can be telecommuting), CDISC programmer/Sr. SAS programmer Analyst, Sr. Clinical Study Manager, Sr. Clinical Outsourcing Consultant , Senior Medical Data Specialist/Medical Dictionary Coding, Sr. Clinical Data Manager, Medical Writer for our pharmaceutical clients in multiple locations inNort...

Hi New Contract Opportunity Sr. SAS Programmer Analyst Major Pharmaceutical Company 12 Months Woodcliff Lake NJ 07677 Sr. SAS Programmer Analyst, Data Operations Position Summary: Accountable for developing programs to create standard reports and listings for clinical data management and other areas of clinical for data review and data cleaning to conduct clinical trials in Oncology area. ...

Qualifications/Skills: BS/MS in Chemistry or related area is required and 5+ years of experience in GC/MS analysis. Demonstrated chromatography skills and hands-on experience in operation, and maintenance of gas chromatography equipment is required. Additional experience in using advanced GC/MS for analysis of flavors and fragrances is preferred. Would consider experience in other industries as...

Company Confidential
Temporary position likely to go full time available at specialty organics material supplier to the flavor and fragrance industry; Qualifications: Degree in chemistry (Advanced Degree preferred) with working knowledge and practice in all aspects of chromatography. Experience with Chemstation a plus, preference given to individuals with flavor and fragrance or allied industry experience. Duties to i...

Company Confidential
North New Jersey Specialty Organic Company requires a PH.D. Organic Chemist for research and development of new products and processes. Company provides medical, dental, bonus and pension plans (the latter two dependant upon individual and company performance). Please fax resume and salary requirements to 973-256-4260....

Everest Clinical Research ("Everest") is a contract research organization providing statistical, data management, statistical programming, medical writing, subject randomization and drug supply management, regulatory submission, and clinical trial management to pharmaceutical, biotechnology, and medical device companies. We serve some of the best-known companies worldwide, and work with many of t...

Everest Clinical Research ("Everest") is a contract research organization providing statistical, data management, statistical programming, medical writing, subject randomization and drug supply management, regulatory submission, and clinical trial management to pharmaceutical, biotechnology, and medical device companies. We serve some of the best-known companies worldwide, and work with many of t...