Rovensa Next North America
Regulatory Affairs Expert
Rovensa Next North America, Fresno, California, United States, 93650
Regulatory Affairs Expert – Overview
The Regulatory Affairs Expert will drive regulatory activities to ensure compliance and market access for Rovensa Next portfolio within North America. Mission
Rovensa Next combines local technical knowledge, innovation and teams that work alongside farmers and distributors in the field to solve sustainability challenges, backed by the global expertise and leadership of the Rovensa Group. It is aimed to shape a sustainable future for agriculture and drive its biotransformation. Let’s grow greener! www.rovensanext.com/ Responsibilities
Prepare, submit and maintain product registration dossiers, labels and related activities in North America Develop and implement registration submission strategy to achieve commercial objectives including advising various departments of data requirements to support product registrations. Create, coordinate and review product technical documents such as labels, supporting literature, and registration dossiers. Ensure that Rovensa Next product labelling, classification and sales comply with local regulations, provide relevant risk analysis in the region and initiate corrective measures when needed. Evaluate and advise on raw materials, formula changes, monitor product conformity, compliance and assist with internal audits requiring regulatory input. Contract and monitor third part laboratory studies (e.g., acute toxicity, agricultural residues, heavy metals) as needed to support regional product registrations. Conduct scientific data review. Liaise and co‑operate with global regulatory team for product registrations and special projects. Identify, troubleshoot, and increase efficiency in areas of improvement/potential problems and development of policies and procedures to meet regulations and requirements. Keep up‑to‑date knowledge of local regulations: national regulations on fertilizers, biostimulants, plant protection products, organic farming standards, other horizontal regulations and their trends. Perform other related tasks as assigned. Qualifications
Requires a Bachelor’s degree in relevant scientific discipline (biological science, chemistry, or toxicology etc.). Master’s degree is highly preferred. 5 years proven professional experience in a similar agrochemical regulatory environment. Excellent knowledge of regulatory requirements for agricultural crop remedies, including nutrition, bio‑stimulants, bio‑pesticides and/or adjuvants. Basic knowledge of import, export and transport regulations including DOT, IMDG, IATA, EPA, TSCA, FDA, and USDA. Experience with interpreting technical material such as trial and toxicology reports. Ability to work independently and in a team environment. Analytical person with creative and strategic thinking. Equal Opportunity
Rovensa Group is an equal‑opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws. This policy applies to all employment practices within our including hiring, recruiting, promotion, termination, layoff, recall, leave of absence, compensation, benefits, training, and apprenticeship. Rovensa Group makes hiring decisions based on qualifications, merit, and business needs at the time.
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The Regulatory Affairs Expert will drive regulatory activities to ensure compliance and market access for Rovensa Next portfolio within North America. Mission
Rovensa Next combines local technical knowledge, innovation and teams that work alongside farmers and distributors in the field to solve sustainability challenges, backed by the global expertise and leadership of the Rovensa Group. It is aimed to shape a sustainable future for agriculture and drive its biotransformation. Let’s grow greener! www.rovensanext.com/ Responsibilities
Prepare, submit and maintain product registration dossiers, labels and related activities in North America Develop and implement registration submission strategy to achieve commercial objectives including advising various departments of data requirements to support product registrations. Create, coordinate and review product technical documents such as labels, supporting literature, and registration dossiers. Ensure that Rovensa Next product labelling, classification and sales comply with local regulations, provide relevant risk analysis in the region and initiate corrective measures when needed. Evaluate and advise on raw materials, formula changes, monitor product conformity, compliance and assist with internal audits requiring regulatory input. Contract and monitor third part laboratory studies (e.g., acute toxicity, agricultural residues, heavy metals) as needed to support regional product registrations. Conduct scientific data review. Liaise and co‑operate with global regulatory team for product registrations and special projects. Identify, troubleshoot, and increase efficiency in areas of improvement/potential problems and development of policies and procedures to meet regulations and requirements. Keep up‑to‑date knowledge of local regulations: national regulations on fertilizers, biostimulants, plant protection products, organic farming standards, other horizontal regulations and their trends. Perform other related tasks as assigned. Qualifications
Requires a Bachelor’s degree in relevant scientific discipline (biological science, chemistry, or toxicology etc.). Master’s degree is highly preferred. 5 years proven professional experience in a similar agrochemical regulatory environment. Excellent knowledge of regulatory requirements for agricultural crop remedies, including nutrition, bio‑stimulants, bio‑pesticides and/or adjuvants. Basic knowledge of import, export and transport regulations including DOT, IMDG, IATA, EPA, TSCA, FDA, and USDA. Experience with interpreting technical material such as trial and toxicology reports. Ability to work independently and in a team environment. Analytical person with creative and strategic thinking. Equal Opportunity
Rovensa Group is an equal‑opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws. This policy applies to all employment practices within our including hiring, recruiting, promotion, termination, layoff, recall, leave of absence, compensation, benefits, training, and apprenticeship. Rovensa Group makes hiring decisions based on qualifications, merit, and business needs at the time.
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