Monsanto Regulatory Information Management Specialist in ST. LOUIS, Missouri
We are seeking highly motivated Regulatory
Documentation Specialists for current and future roles to join the
Regulatory Affairs Team.
In this role, you will support the
development and implementation of regulatory processes, compilation of product
dossiers, agency submissions, and will contribute to efforts to obtain and
maintain U.S. and global regulatory approvals for agrochemicals, biologs and/or
biotechnology derived products across our robust pipeline and business
units. You will work closely with colleagues as new products are
handed-off to regulatory, fully-characterized to ensure product safety, and
ultimately commercialized for sale and distribution.
This position will work in a
cross-functional capacity to implement approval strategies to obtain both U.S.
and international regulatory approvals. The position will utilize your document
management skills, keen eye for quality, and strong process orientation to
provide input on regulatory dossiers, and prepare documents to support product
registrations in the U.S. and other countries.
Support global regulatory strategies for our productsin collaboration with colleagues in the global Regulatory organization
Provide input and coordination in informationmanagement for Regulatory Affairs. Manage regulatory documentationprocesses to ensure thatappropriate national (e.g., USDA, EPA, FDA), State/Territory, andinternational data (e.g., CODEX, OECD) requirements are met
Assist in the preparation of regulatory submissions,edit submissions, coordinate responses to questions from regulatoryauthorities, develop product composition statements, certificates oforigin, production reports, develop product labeling, and support the developmentof other related documents (e.g., white papers, position statements, etc)to obtain regulatory approvals in the US and other markets
Improve internal regulatory processes and manageinformation databases
Filing, archiving, uploading and viewingRegulatory documents
Minimum of a Bachelor’s degree, or professional degree equivalentthrough experience
One or more years of relevant experience in theagricultural, chemical, biotechnology, pharmaceutical or relatedscientific based industry
Excellent written/oral communication and organizationskills
Proficient with IT tools and databases, and mastery ofMicrosoft Office suite of applications
Strong project management skills, and the ability tosuccessfully interact with a wide diversity of people
Prior experience working for a life sciences company
Prior experience working in a regulated environment forbiological, agrochemical, chemical, biotechnology, or pharmaceuticalproducts
Bayer successfully completed the
acquisition of Monsanto in June 2018, bringing together Monsanto’s leadership
in seeds and plant traits with Bayer’s leadership in chemical and biological
crop protection. By joining forces, we will create even more extensive career
opportunities for talent around the world. We’re a global team working to shape
agriculture through breakthrough innovation that will benefit farmers,
consumers, and our planet.
While we are now Bayer, we will continue to hire using separate career sites
until we can integrate our career platforms. We invite you to explore the
career opportunities available at the combined company by visiting
Organization: Global Chemical Regulatory Affairs51096759_
Title: Regulatory Information Management Specialist
Location: North America-USA-Missouri-St. Louis
Requisition ID: 01TEV
Job: Research & Development
At Monsanto, we value a diverse combination of ideas, perspectives and cultures. All qualified applicants will receive consideration for employment without regard to, among other things, race, religion, color, national origin, age, sex, sexual orientation, gender identity, gender expression, status as a protected veteran, or status as a qualified individual with a disability. If you need a reasonable accommodation to access the information provided on this website, please for further assistance.access our disability accommodations process
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