Community affairs jobs in Plainfield, NJ

At least 8 10 years of relevant pharmaceutical biotechnology experience in R&D, including at least 5 years of relevant Regulatory Affairs experience (regional and or global), in early..

Job Details. Internal Job Title. Regulatory Affairs Associate II Duration. 12 months. Contract Location. Onsite. Clark, NJ Key Responsibilities Review formulas for compliance with local..

Job Tittle. Medical Affairs Manager Duration. 12. Months Location. Titusville, NJ (Hybrid OR Remote can.. Partnership across Medical Affairs, RW V&E, JRD, Brand Marketing, Regulatory Affairs, Global Medical..

Regulatory Affairs Associate located in Clark, NJ. Details for the position are as follows. Pay Rate. 25.74 hr. Job Description Responsibilities. This is an entry level position within R&I..

JOB SUMMARY. The Regulatory Affairs Manager will be responsible for independently compiling and.. The Regulatory Affairs Manager is a self motivated, detail oriented, flexible team player who is able to..

months with the possibility of extension Intake Call Notes. This is an entry level position within R&I. It is not a lab based role, but rather a corporate 'desk job' supporting r..

JOB SUMMARY. The Regulatory Affairs Manager will be responsible for independently compiling and.. The Regulatory Affairs Manager is a self motivated, detail oriented, flexible team player who is able to..

Position requires a Bachelor's degree in a science or chemistry related field, coursework or certification in Cosmetic or Drug Regulatory Affairs Experience in drug or cosmetic industry..

We are proud to offer an opportunity to work as a Sr Scientist, Regulatory Affairs located in Clark, NJ.. 0 60 hr Purpose of the Role. Administer regulatory affairs over the product lifecycle from pre market..

We are proud to offer an opportunity to work as a Sr Scientist, Regulatory Affairs located in Clark, NJ.. It's the ripple effect that changes and improves everything for your family, your community, and the..

Innovating every day. Position Overview The Senior Director, Regulatory Affairs will lead and formulate.. Supervise 3 regulatory affairs specialists. Position Requirements Must have a master's degree in..

Take a shot at us for your IT requirements and experience a radical change. Job Description Accountable for deliverables of the Global Medical Affairs function, including expert review and..

The Senior Director, Regulatory Affairs will lead and formulate the regulatory affairs strategy for.. Supervise 3 regulatory affairs specialists. Position Requirements Must have a master's degree in..

The requirement is for 3 Regulatory Affairs Specialist.Responsibilities. Identify reference documents for technical documentation including, but not limited to design and risk documents..

Experience Qualifications. 10 or More Years in the pharmaceutical industry required. 7 or More Years in regulatory affairs Experience in providing regulatory strategic input into the drug..

Associate Director, Regulatory Affairs UK The Regulatory Affairs team manages a broad portfolio of.. A new opportunity has arisen in the UK Regulatory Affairs Department, at the Associate Director level..

About Us Evergreen Theragnostics, Inc. is a radiopharmaceutical company headquartered in Springfield, NJ. We operate in a brand new state of the art facility, providing contract de..

The Director of Statistical Programming Medical Affairs provides leadership to the group in Medical.. membership of the Traveler community, sexual orientation, disability, genetic information, familial..