Regulatory Specialist/Lead

POSITION: Regulatory Lead (Registration Documentation) - Any candidate must have previous 5 years at least experince about registration of the biopesticides and biostimulnats in UK and EU.

LOCATION: Port Talbot, UK

DURATION: 6 months - 36 Month Contract 

Employment Type: Full-time 

Description:

Crop IQ is a global, science-led biotechnology company that made up of dedicated pioneers who manufacturing cutting-edge, innovative, sustainable farming solutions that utilize natural ingredients and integrated pest management (IPM) strategies to create additional value for all the stakeholders in the farming sector: farmers, suppliers and consumers.

Job Summary:

The Regulatory Specialist is responsible for preparing, reviewing, and submitting product registration documents to ensure compliance with local and international regulations. The ideal candidate must have a strong background in chemistry and experience in regulatory affairs (apprentices with relevant education will be considered).

Key Responsibilities:

1. Prepare registration docs of every single product according to EU and local regulatory requirements.

2. Audit external suppliers, distributors, or partners against regulatory standards.

3. Investigate compliance failures or product quality issues in the broader supply chain.

4. Rectify non-compliance by developing corrective actions and ensuring they are implemented effectively at external sites.

5. Registration Document Preparation:

   • Compile, review, and submit regulatory dossiers for chemical products (e.g., pharmaceuticals, agrochemicals, industrial chemicals).
   • Ensure compliance with regulations (REACH, FDA, EPA, GHS, CLP, EPA etc.).
   • Maintain up-to-date knowledge of regulatory requirements.
6. Regulatory Compliance:
   • Monitor changes in regulations and update documentation accordingly.
   • Liaise with regulatory authorities and respond to queries.
   • Ensure proper labeling and Safety Data Sheets (SDS) compliance.
7. Technical & Scientific Support:
   • Interpret chemical data (composition, stability, toxicity) for regulatory submissions.
   • Collaborate with R&D and quality teams to ensure product compliance.
8. Project Management:
   • Track submission timelines and deadlines.
   • Maintain organized records of regulatory documents.
9. Communication & Reporting:
   • Prepare internal reports on regulatory status.
   • Train internal teams on compliance requirements.

Required Skills & Qualifications:

Education & Experience:

• Minimum  Level 4 regulatory Compliance apprenticeship. https://www.alstraining.org.uk/regulatory-compliance/
• Familiarity with regulatory frameworks (EU, US, or other regions).

Technical Skills:

• 5 years minimum experince in registration docs of the Semiochemicals mating disruption, mass trapping and attract and kill.
• Experienced in the publiv health products in UK and EU.
• Strong understanding of chemical properties and regulatory requirements.
• Experience with SDS, GHS, and product classification.
• Proficiency in regulatory submission software/tools (e.g., IUCLID, REACH-IT).
• Advanced MS Office skills (Word, Excel, PowerPoint).

Soft Skills:

• Excellent attention to detail.
• Strong analytical and problem-solving abilities.
• Effective communication (written and verbal).
• Ability to work under tight deadlines.

Preferred Qualifications (Not Mandatory):

• Experience in pharmaceutical or agrochemical regulatory submissions.
• Knowledge of toxicology or ecotoxicology studies.
• Certification in regulatory affairs (e.g., RAC).

Opportunities for Growth:

• Joining a fast growing company with a global teamwork.
• Career advancement in regulatory leadership roles.
• Please send your resume to info@cropiqtech.com

                                             career@cropiqtech.com