Regulatory Affairs Specialist at Savant Chemicals Catalunya

Further Details

Savant Chemicals is now recruiting in Catalunya. Apply for the position of Regulatory Affairs Specialist. The required qualification is Bachelor. This role is within the Chemicals industry. A bachelor degree is preferred. The application process commenced on 03 November, 2026 via Eurojobs. Interested and eligible candidates must submit their applications before the deadline on 18 December, 2026. This is a prime opportunity to join a renowned organization. For a step-by-step application guide and full eligibility criteria, please see the official advertisement on https://www.jobseed.pk.

Regulatory Affairs Specialist at Savant Chemicals

We have an immediate opening for the post of Regulatory Affairs Specialist. The job location is Catalunya.

Key Requirements:

• Qualification: Bachelor
• Vacancies: 1

This is a fantastic chance to work with a reputed organization and grow professionally.

Skills

• Manage technical and regulatory documentation for chemical raw materials
• Review and update safety data sheets (SDS/FDS) and technical data sheets (TDS)
• Handle certificates of analysis (CoA) and other product-specific documentation
• Ensure proper organization, archiving, and version control of documents
• Monitor compliance with REACH and CLP regulations in Europe
• Track legislative changes affecting the product catalog
• Verify regulatory requirements for different markets and applications
• Liaise with national and international suppliers for regulatory information
• Respond to technical and documentation inquiries from clients
• Collaborate with sales teams to provide product technical information
• Support quality management systems and relevant certifications (e.g., ISO)
• Assist in preparing documentation for audits and supplier homologations
• Contribute to the improvement of internal procedures
• Manage documentation for sample dispatch
• Strong proficiency in office software, especially Excel
• Good written and spoken English communication skills

Duties and Responsibilities:

• Manage, review, and maintain up-to-date technical and regulatory documentation for our chemical raw material catalog
• Request, verify, and update safety data sheets (SDS/FDS), technical data sheets (TDS), certificates of analysis (CoA), and other product documentation
• Manage declarations of conformity, certificates of origin, composition, allergens, and other customer-specific documents
• Ensure accurate organization, archiving, version control, and traceability of all documentation
• Guarantee the availability of necessary documentation for the commercialization and distribution of our products
• Oversee compliance with applicable regulatory requirements for marketed products
• Review documentation related to European REACH and CLP regulations, including classification, labeling, and hazard communication for substances and mixtures
• Track new and modified legislation that may impact our product catalog
• Verify specific regulatory requirements for different markets and product applications
• Collaborate in identifying and resolving potential regulatory incidents or deviations
• Provide technical and regulatory support for the incorporation of new raw materials and suppliers
• Act as a technical point of contact for requesting and managing regulatory documentation with national and international suppliers
• Respond to technical and documentary inquiries from our clients
• Manage quality questionnaires, homologation forms, and regulatory information requests
• Collaborate with the commercial team to facilitate technical product information and applications
• Ensure agile and efficient communication between suppliers, clients, and internal teams
• Support the maintenance and monitoring of the company's quality management systems
• Manage documentation related to applicable standards and certifications, such as ISO, GMP+, and other sector-specific standards
• Participate in the documentary preparation for internal and external audits, as well as supplier homologation processes
• Contribute to the development, updating, and improvement of internal procedures
• Collaborate in the management of incidents, non-conformities, and corrective actions related to documentation and regulatory compliance
• Oversee the technical and regulatory documentation required for the management and shipment of samples to clients
• Coordinate with Customer Service, Purchasing, Sales, and Logistics departments to ensure correct document management
• Verify the documentary and labeling requirements applicable to products and samples
• Provide support in the documentary evaluation of new references and commercial opportunities

How to apply

How to Apply for Regulatory Affairs Specialist:

• 💼 Prepare Your Application: Ensure your Curriculum Vitae (CV) and any relevant supporting documents are up-to-date.
• 🎓 Verify Qualifications: Confirm you meet the degree requirement of a university degree in Chemistry, Chemical Engineering, Biochemistry, Pharmacy, or a similar scientific discipline.
• 🔎 Review Experience: Ensure you have previous experience in Regulatory Affairs, quality management, or similar technical documentation roles within the chemical industry.
• 🌍 Language Proficiency: Confirm your good command of both written and spoken English for international communication.
• 👉 Visit the Application Portal: Navigate to the official application link provided below.
• 📝 Complete the Online Application: Fill out all required fields accurately on the application form.
• 🚀 Submit Your Application: Click the 'Apply Now' button to submit your application for the Regulatory Affairs Specialist position.
• ⏳ Application Deadline: Please ensure your application is submitted by the closing date of 18 December 2026.
• Important Note: Only shortlisted candidates will be contacted for further selection stages.