Regulatory Affairs Manager

HIRING: Regulatory Affairs Manager - Growing Global Pharma - New Jersey
Hays Life Sciences is currently partnered with a growing global pharmaceutical company to assist in their search for a Regulatory Affairs Manager to be based in New Jersey. This company is advancing their developmental efforts for both small molecule and biologic products. Focused in a variety of therapeutic areas, this company’s innovative business is looking to make big strides in 2019. The Regulatory Affairs Manager is an important addition to the Regulatory Affairs team.

In this capacity, you will be responsible for leading the authoring, preparation, review and submission of regulatory documents and dossiers to regulatory authorities including IND, NDA, ANDA, amendments, supplements, annual reports, briefing documents and meeting requests. You will assist with the design of regulatory strategies, serve as a regulatory contact with health authorities and provide regulatory assessments of manufacturing processes. In addition, you will manage technical quality control of documents.

At minimum, you must possess a Bachelor’s degree in a Scientific discipline, 5+ years of Regulatory Affairs pharmaceutical industry experience, and eCTD regulatory submissions experience.

Apply now for consideration.


Job type:
Full Time
New Jersey
Competitive / Based on Experience
Apply Now

Talk to a consultant

Talk to Phu Huynh, the specialist consultant managing this position, located in New York

23rd Floor, 555 Eighth Avenue, New York, NY, United States of America, 10018-4378

Telephone: 212 548 4525

Share Job