Job Overview

We are seeking a highly experienced and knowledgeable Senior Manager Regulatory Affairs - Agrochemical & International Registration to join our team. As the Senior Manager Regulatory Affairs, you will be responsible for overseeing all regulatory compliance and strategy related to agrochemical products. This is a senior leadership role that requires strong regulatory expertise, team management skills, and exceptional communication abilities.

Roles and Responsibilities

• Develop and implement regulatory strategies and plans to ensure compliance with agrochemical regulations
• To handle the international registration process of the organization.
• Provide guidance and support to cross-functional teams on regulatory requirements
• Manage the preparation and submission of regulatory submissions, including dossiers, registrations, and notifications
• Monitor and stay up-to-date with regulatory changes and assess their impact on the business
• Conduct risk assessments and develop mitigation strategies
• Collaborate with internal stakeholders and external partners to ensure regulatory compliance across all stages of product development and post-market activities
• Lead and mentor a team of regulatory professionals
• Represent the company in regulatory meetings and negotiations with regulatory authorities
• Provide regulatory input and support to product development teams
• Ensure compliance with FDA regulations and other relevant regulatory standards
• Manage relationships with regulatory agencies and keep abreast of regulatory trends and best practices

Qualifications and Skills

• Bachelor's degree in a relevant scientific or regulatory discipline
• Minimum of 10-15 years of experience in regulatory affairs within the agrochemical industry
• Strong knowledge of agrochemical regulations, including EPA and other global regulatory requirements
• Experience in developing and implementing regulatory strategies
• Proven track record of successful regulatory submissions and approvals
• Excellent communication skills, both written and verbal
• Strong project management abilities with the ability to prioritize and meet deadlines
• Effective leadership and team management skills
• Analytical and critical thinking abilities
• Ability to navigate complex regulatory requirements and adapt to changes
• Knowledge of FDA regulations and pharmaceutical industry practices
• Ability to work independently as well as collaboratively in a cross-functional environment
• Attention to detail and accuracy