Compliance

• Support the management of crop protection product registration dossiers under EU Regulation 1107/2009
• Review regulatory dossiers to ensure compliance with client quality standards and EU requirements
• Act as a liaison to collect and manage registration requirements and contribute to business process development with regulatory experts across Europe
• Work with the Europe Regulatory Manager and project teams to obtain and maintain EU Member State authorizations for crop protection products
• Represent regulatory and safety positions in project teams and facilitate business decisions
• Manage relationships with internal and external stakeholders, including regulatory authorities and cross-functional teams
• Lead planning, submission, and post-submission activities for new formulations and product renewal programs
• Develop project plans to ensure timely and quality delivery of regulatory submissions
• Contribute expertise to improve regulatory processes and lead initiatives for efficient ways of working
• Share knowledge and mentor others as your experience grows
• Coordinate and manage team members working remotely to ensure that productivity, quality, documentation, working hours, and excellence are managed to maximum efficiency

Regulatory Affairs Specialist – Group Leader, Crop Protection

Regulatory Affairs Manager – Clinical Trial Applications