Regulatory Dossier Writer in Norwich

Are you a plant scientist with expertise in molecular biology and/or gene-editing? Do you enjoy technical writing and applying your scientific knowledge outside of the laboratory? We are looking to add a Regulatory Dossier Writer to Tropic’s international team as we expand into new global territories. Reporting to the Head of Regulatory, the Regulatory Dossier Writer will develop and submit regulatory dossiers to secure field trial permits and exemptions from GMO regulations for Tropic’s gene-edited products. You will join a cross-functional team supporting Tropic’s product development and commercialisation efforts.

The Regulatory Dossier Writer will create and manage the development of dossiers required to gain regulatory approvals to conduct field trials of biotech crops and to commercialise gene-edited products. They will interpret complex scientific data and other technical information, translating them into clear, accurate and compliant regulatory documents. The ideal candidate will possess strong expertise in plant biotechnology and gene editing technologies, with an understanding of regulations relating to GMOs and gene-edited products, and a proven ability to write and manage complex documents while working cross-functionally.

Responsibilities:

• Write and coordinate the revision and completion of dossiers such as field trial permit applications, exemption requests and regulatory internal filings (e.g., self-determinations).
• Ensure regulatory dossiers align with Tropic’s regulatory strategy, including navigating complex regulatory requirements in different regions.
• Liaise with internal teams, external consultants, and regulatory bodies to gather information and facilitate dossier development and submission.
• Ensure all documents are complete, accurate and in compliance with relevant global regulatory frameworks, including content specifications, terminology and formatting.
• Compile, develop and manage the revision and submission of answers to regulators’ questions and requests for further information.
• Identify and propose solutions to regulatory challenges, ensuring smooth progression through the submission and approval process.
• Stay updated on changing regulatory requirements and industry best practices to ensure dossiers are always in compliance.
• Clearly communicate and report progress and updates to internal and external stakeholders.
• Define and document processes for effective management of dossier development, revisions, and internal records.
• Maintain an organized system for tracking dossier development and submission timelines, key post-submission activities and approvals.
• Maintain a repository of all relevant regulatory documents including document templates, dossiers, regulatory determinations and approval letters.
• Contribute to the preparation and execution of meetings with regulators and regulatory audits and inspections (e.g., Plant Breeding Innovation Management Program).

Requirements:

Qualifications: PhD in Plant Biotechnology, Plant Molecular Biology, Agricultural Science, or related fields (or MSc with at least 3 years of relevant experience).

Essential Skills:

• Strong expertise in plant biology and biotechnology, molecular biology and/or gene editing technologies in agriculture.
• Familiarity with global regulatory requirements for biotech crops.
• Excellent technical writing skills with the ability to present complex regulatory information clearly; experience delivering high-quality formal documents.
• Proficiency with document preparation software such as Microsoft Word.
• Strong interpersonal skills to communicate with subject matter experts, regulatory stakeholders, and internal teams.
• Attention to detail and ability to ensure scientific data is accurately presented and regulatory guidelines and formatting standards are followed.
• Strong critical thinking and problem-solving skills to address regulatory gaps or misalignments.
• Excellent organizational, planning and project management abilities to manage multiple priorities and meet deadlines.
• Ability to work independently and as part of a cross-functional, fast-paced team.
• Resilience and flexibility to adjust dossier preparation to project requirements and regulatory changes.

Desirable Skills:

• Direct experience in agricultural biotechnology or gene editing.
• Experience creating and managing regulatory dossiers.
• Knowledge of biosafety, environmental impact assessments, and food safety considerations for biotech crops.
• Experience with document management systems and processes.
• Fluency in Spanish is beneficial but not essential.

About Us: Tropic is one of the world’s leading agricultural gene-editing companies. Our team develops and commercialises high-performing tropical crop varieties to benefit growers, processors and consumers globally, addressing real-world problems around food security and sustainability. Our vision is to become a leading seed business with significant product ownership from laboratory to field, while maintaining relationships with growers and consumers based on transparency and trust.

Why Join Tropic?

• Diverse workforce in a dynamic environment
• Excellent learning and career development opportunities
• Social events throughout the year
• Competitive compensation and benefits including Private Medical Care and Medical Cash Plan
• 25 days annual leave and Life Assurance

Further Information:

• Job Location – Norwich
• Time Requirement – Full Time
• Contract – Permanent
• Closing date – 9th July 2026