Regulatory Dossier Writer

{
  "content_hash": "41acf7a9ec4a65386de26bd8efe7561fe7f4d09001abe6bdbf7afb2cc06ccd6e",
  "source_hash": "e889f99e935731a360287bd3bd15fab4fcebed55febaaec3fb793a0b60304e62",
  "last_changed_at": "2026-06-20T10:56:49.035Z",
  "active_status": "active"
}

{
  "dedupe": null,
  "language": "en",
  "location": {
    "raw": "Norwich, Norfolk, NR4 7GJ, United Kingdom",
    "city": "Norwich",
    "region": "Norfolk",
    "country": null,
    "is_remote": false,
    "confidence": 0.8
  },
  "salary_max": null,
  "salary_min": null,
  "inferred_at": "2026-06-20T10:56:49.035Z",
  "launch_scope": {
    "reason": "bamboohr_production_catalog",
    "included": true,
    "location": {
      "raw": "Norwich, Norfolk, NR4 7GJ, United Kingdom",
      "city": "Norwich",
      "region": "Norfolk",
      "country": null,
      "is_remote": false,
      "confidence": 0.8
    },
    "countries": []
  },
  "remote_policy": null,
  "salary_period": null,
  "workplace_type": null,
  "salary_currency": null
}

{}

{
  "list_job": {
    "id": "242",
    "isRemote": null,
    "location": {
      "city": "Norwich",
      "state": "Norfolk"
    },
    "atsLocation": {
      "city": null,
      "state": null,
      "country": null,
      "province": null
    },
    "departmentId": "18930",
    "locationType": "0",
    "jobOpeningName": "Regulatory Dossier Writer",
    "departmentLabel": "IP & Regulatory",
    "employmentStatusLabel": "Full-Time"
  },
  "detail_errors": [],
  "detail_job_opening": {
    "location": {
      "city": "Norwich",
      "state": "Norfolk",
      "postalCode": "NR4 7GJ",
      "addressCountry": "United Kingdom"
    },
    "datePosted": "2026-06-19",
    "atsLocation": {
      "city": null,
      "state": null,
      "country": null,
      "countryId": null
    },
    "description": "<p><span style=\"font-weight: bold\">Are you a plant scientist with expertise within molecular biology and/or gene-editing?</span></p>\n<p><br></p>\n<p>Do you enjoy technical writing and applying your scientific knowledge outside of the laboratory? Are you interested in joining a fast-paced, innovative agricultural biotechnology company as a Regulatory Dossier Writer?</p>\n<p> </p>\n<p>As Tropic continues to grow into new global territories, we are looking to add an additional Regulatory Dossier Writer into our international team. <br><br>Reporting to the Head of Regulatory, the Regulatory Dossier Writer will play a crucial role in developing and submitting regulatory dossiers to secure field trial permits and exemptions from GMO regulations for Tropic’s gene-edited products.</p>\n<p><br></p>\n<p>You will join a cross-functional dynamic team working to successfully enable Tropic’s product development and commercialisation efforts.  </p>\n<p> </p>\n<p><span style=\"font-size: 12pt; font-weight: bold\">Job Purpose</span><br></p>\n<p><br></p>\n<p>The Regulatory Dossier Manager 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.</p>\n<p> </p>\n<p>The ideal candidate will possess strong expertise in plant biotechnology and gene editing technologies, strong interest in and understanding of regulations relating to GMOs and gene-edited products along with a proven ability to write and manage complex documents while working cross-functionally to support the development of innovative agricultural products.</p>\n<p> </p>\n<p><span style=\"font-size: 12pt; font-weight: bold\">Responsibilities</span></p>\n<p> </p>\n<ul>\n<li>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).</li>\n</ul>\n<p> </p>\n<ul>\n<li>Ensure regulatory dossiers align with Tropic’s regulatory strategy, including navigating complex regulatory requirements in different regions.</li>\n</ul>\n<p> </p>\n<ul>\n<li>Liaise with internal teams, external consultants, and regulatory bodies to gather all relevant information and to facilitate efficient dossier development and submission.</li>\n</ul>\n<p> </p>\n<ul>\n<li>Ensure all documents are complete, accurate and in compliance with relevant global regulatory frameworks, including content specifications, terminology and formatting.</li>\n</ul>\n<p> </p>\n<ul>\n<li>Compile, develop and manage the revision and submission of answers to regulators’ questions and requests for further information.</li>\n</ul>\n<p> </p>\n<ul>\n<li>Identify and propose solutions to regulatory challenges, ensuring smooth progression through the submission and approval process.</li>\n</ul>\n<p> </p>\n<ul>\n<li>Stay updated on changing regulatory requirements and industry best practices to ensure dossiers are always in compliance.</li>\n</ul>\n<p> </p>\n<ul>\n<li>Clearly communicate and report progress and relevant updates to internal and external stakeholders.</li>\n</ul>\n<p> </p>\n<ul>\n<li>Define and document processes for effective management of dossier development, revisions, and internal records.</li>\n</ul>\n<p> </p>\n<ul>\n<li>Maintain an organized system for tracking dossier development and submission timelines, key post submission activities and approvals.</li>\n</ul>\n<p> </p>\n<ul>\n<li>Maintain a repository of all relevant regulatory documents including document templates, dossiers, regulatory determinations and approval letters.</li>\n</ul>\n<p> </p>\n<ul>\n<li>Contribute to the preparation and execution of meetings with regulators and regulatory audits and inspections (e.g., Plant Breeding Innovation Management Program).</li>\n</ul>\n<p> </p>\n<p><span style=\"font-size: 12pt; font-weight: bold\">Requirements</span></p>\n<p> </p>\n<p><span style=\"text-decoration: underline\">Qualifications:</span></p>\n<p> </p>\n<ul>\n<li>PhD degree (or MSc degree with at least 3 years of relevant work experience) in Plant Biotechnology, Plant Molecular Biology, Agricultural Science, or related fields.</li>\n</ul>\n<p> </p>\n<p><span style=\"text-decoration: underline\">Essential skills:</span></p>\n<p> </p>\n<ul>\n<li>Strong expertise in plant biology and biotechnology, molecular biology and/or gene-editing technologies applied in agriculture.</li>\n</ul>\n<p> </p>\n<ul>\n<li>Familiarity with global regulatory requirements for biotech crops.</li>\n</ul>\n<p> </p>\n<ul>\n<li>Excellent technical writing skills, with ability to present complex regulatory information clearly and demonstrated experience delivering high quality formal documents.</li>\n</ul>\n<p> </p>\n<ul>\n<li>Proficiency with software tools for document preparation, such as Microsoft Word.</li>\n</ul>\n<p> </p>\n<ul>\n<li>Strong interpersonal skills and ability to clearly communicate with subject matter experts, regulatory stakeholders, and internal teams to gather information, ensure alignment on requirements and provide updates on progress.</li>\n</ul>\n<p> </p>\n<ul>\n<li>Excellent attention to detail and ability to ensure that scientific data is accurately presented and that all regulatory guidelines and formatting standards are followed.</li>\n</ul>\n<p> </p>\n<ul>\n<li>Strong critical thinking skills and effective problem-solving with ability to identify gaps or misalignments in regulatory data or documents and address them in a regulatory-appropriate manner.</li>\n</ul>\n<p> </p>\n<ul>\n<li>Strong organizational, planning and project management skills to effectively manage multiple priorities and meet deadlines.</li>\n</ul>\n<p> </p>\n<ul>\n<li>Ability to work independently and collaboratively as part of a cross-functional dynamic team in a fastpaced environment.</li>\n</ul>\n<p> </p>\n<ul>\n<li>Resilience and flexibility to adjust dossier preparation according to project requirements, commercial activities, the regulatory authority involved, and/or changes in the regulatory landscape and guidelines.</li>\n</ul>\n<p>  </p>\n<p><span style=\"text-decoration: underline\">Desirable skills:</span></p>\n<p> </p>\n<ul>\n<li>Direct work experience in agricultural biotechnology or gene editing.</li>\n</ul>\n<p> </p>\n<ul>\n<li>Experience creating and managing regulatory dossiers.</li>\n</ul>\n<p> </p>\n<ul>\n<li>Knowledge of biosafety, environmental impact assessments, and food safety considerations for biotech crops.</li>\n</ul>\n<p> </p>\n<ul>\n<li>Experience with document management systems and processes.</li>\n</ul>\n<p><br></p>\n<ul>\n<li>Fluency in Spanish is beneficial but not essential.</li>\n</ul>\n<p> </p>\n<p><span style=\"font-size: 12pt; font-weight: bold\">About Us</span></p>\n<p> </p>\n<p>Tropic is one of the world’s leading agricultural gene-editing companies. Our team is dedicated to the development and commercialization of high-performing varieties of tropical crops to provide significant benefits to growers, processors and consumers globally, tackling real-world problems around food security and sustainability.</p>\n<p><br>Our vision is to become a leading seed business with significant ownership of its products from the laboratory to the field, while maintaining constructive relationships with growers and consumers based on transparency and trust.</p>\n<p> </p>\n<p><span style=\"font-weight: bold\">Why Join Tropic? </span></p>\n<p><br></p>\n<ul>\n<li>Diverse workforce operating in a dynamic working environment</li>\n<li>Excellent learning and career development opportunities</li>\n<li>Social events throughout the year</li>\n<li>Competitive compensation and benefits including Private Medical Care, Medical Cash Plan.</li>\n<li>25 days annual leave and Life Assurance</li>\n</ul>\n<p><br></p>\n<p><span style=\"font-size: 12pt; font-weight: bold\">Further Information</span></p>\n<p> </p>\n<ul>\n<li><span style=\"font-weight: bold\">Job Location</span> – Norwich UK </li>\n<li><span style=\"font-weight: bold\">Time Requirement</span> – Full Time</li>\n<li><span style=\"font-weight: bold\">Contract </span>– Permanent</li>\n<li><span style=\"font-weight: bold\">Closing date</span> – 9th July 2026</li>\n</ul>",
    "compensation": null,
    "departmentId": "18930",
    "locationType": "0",
    "seekPromoted": false,
    "jobCategoryId": null,
    "jobOpeningName": "Regulatory Dossier Writer",
    "departmentLabel": "IP & Regulatory",
    "jobOpeningStatus": "Open",
    "minimumExperience": "Mid-level",
    "jobOpeningShareUrl": "https://tropicbioscience.bamboohr.com/careers/242",
    "employmentStatusLabel": "Full-Time"
  }
}