Regulatory Affairs Manager

GreenLight Biosciences is seeking a highly motivated Regulatory Affairs Manager to join our Crop Protection team. Greenlight is developing cutting edge RNA technologies that address key challenges in global Crop Protection. In this role you will be integrally involved in the development and registration of novel biochemical products. The ideal candidate will have registration experience as well as knowledge of biochemical product regulations. Strong technical, organizational, and communication skills, attention to detail, as well as the ability to maintain a commitment to excellence and high-quality work in a fast-paced milestone driven company, are essential.

Responsibilities:

Support supervisor in all aspects of international, federal and state development and registration for GreenLight products. This process typically involves:

Working with regulatory team to plan, assist and manage electronic submission packages to regulatory authorities (e.g.: EPA CDX);

Assure compliance with US Environmental Protection Agency (EPA), Canada Pest Management Agency (PMRA) and other regulatory authorities regulations related to formatting and organizing documents files in preparation for submission to these regulatory authorities.

Work with internal stakeholders to assist annual reports required by authorities (e.g.: EPA Pesticide production establishment reports).

Prepare and maintain US State Registrations supporting internal business plan.

Interfacing with the appropriate regulatory agency (EPA, CDPR, etc.) contacts.

Independently preparing more routine submissions.

Maintaining appropriate files and databases to document such activities;

Being regulatory point of contact with other GreenLight team members to meet registration objectives and address regulatory concerns that impact the businesses, such as amending federal and/or state registrations/labels.

Requirements:

master’s degree or higher in a relevant science (preferred);

previous FIFRA experience; US state registration, label management, international and biochemical experience are a plus;

data management system implementation and management.

good communication skills, be highly organized and have a strong attention to detail.

have a good command of the English language, and an ability to do technical writing and critically review documents;

be proficient in using the following: Microsoft Office products (Word, Excel, PowerPoint, Outlook, Smartsheets is a plus); Adobe Acrobat; other software.