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
