Regulatory Affairs Specialist

hace 6 días


Barcelona, España Prinova Europe A tiempo completo

Regulatory Affairs Specialist (Full-time, Permanent) Unlock your potential with Prinova We are Prinova, a leading global supplier of ingredients and premix manufacturing solutions and trusted by the world's best-known food, beverage, and nutrition brands. Part of the NAGASE Group, our expertise lies in Ingredient Distribution, Manufacturing Solutions, and Customized Services. Our global network of colleagues, located in offices and manufacturing facilities around the world, deliver sustainable value-added solutions to our customers. We are recognized for our deep expertise, commitment to excellence, and bold innovation which have earned us a strong reputation as a trusted industry leader. Wherever your career is headed, you'll find direction, opportunity, and belonging with us.  What does Regulatory Affairs Specialist mean at Prinova?Provide in depth review of regulatory matters for food, feed supplements activity in the EU, UK and outside the EU entities for Prinova Europe. Provide training and troubleshooting. Link with authorities, consultants and professional bodies on all regulatory matters. Participate in company compliance initiatives. What's in it for you? Personal growth, including training and development opportunities Discretionary bonus Comapny events  Travel What to expect?Ensure regulatory compliance with food and feed safety, quality and defence as it relates to UK, EU and GFSI (BRC) requirements, Organic, Halal, FAMI QS and Kosher. Monitor changes in legislation and regulatory requirements, proactively assessing the impact on business and updating the senior management team's compliance protocols as necessary. Support the development and implementation of regulatory strategies for existing ingredients and new ingredients/products in the UK and EU regions ensuring compliance to but not limited to Allergens, REACH, Novel food, Packaging Food Contact Materials, Food Law and labelling, Feed laws and labelling, Residues and Contaminants, Natural and Botanical ingredients etc. Provide regulatory review of product compliance when an in-depth analysis/review is needed for the quality department. Example of review provided: Novel food status, specific application status, claims, labelling. Coordinate with authorities for all work required, such as authorisation and licenses. Support the design and maintenance of Prinova Specification, ensure all information is correct and meets relevant EU regulation requirements. Provide training for the quality and technical teams in Europe. Actively support QA department tasks according to workload and priorities, as required. Provide support to the commercial and marketing team to verify regulatory compliance. Assisting, as required, in the management of crises and incidents as part of the management team. Does this sound like you? A successful candidate will have 5+ years of technical or regulatory experience in food, feed or ingredients.Highly analytical, and organised with keen attention to. Must be able to identify problems and provide systematic. Be able to multi-task and have excellent communication skills. Real team player – Must be able to work with senior and junior employees in a professional and inclusive manner. A high level of business English is essential. The successful candidate will be self-motivated Strong administration skills on Microsoft Office Packaging on Windows. Interested? We would love to hear from you. Submit your CV by clicking apply. If you have any further questions, or would like to see the full job description, please email us for an informal chat careers-



  • Barcelona, España ESTEVE A tiempo completo

    Job description: 1. FUNCTIONAL CONTENT Main Role The Regulatory Affairs Specialist will be responsible for managing the regulatory lifecycle of US FDA-approved products, ensuring ongoing compliance and supporting regulatory activities for the ongoing new product development projects. This role requires close collaboration with cross-functional teams...


  • Barcelona, España ESTEVE A tiempo completo

    Join to apply for the Regulatory Affairs Specialist role at ESTEVE .OverviewManage the regulatory lifecycle of US FDA‑approved products, ensuring ongoing compliance and supporting regulatory activities for new product development projects. Work closely with cross‑functional teams including Global Regulatory, clinical, pharmacovigilance, and external...


  • Barcelona, Barcelona, España ESTEVE A tiempo completo

    Job description:1. FUNCTIONAL CONTENTMain RoleThe Regulatory Affairs Specialist will be responsible for managing the regulatory lifecycle of US FDA-approved products, ensuring ongoing compliance and supporting regulatory activities for the ongoing new product development projects.This role requires close collaboration with cross-functional teams including...


  • Barcelona, España CooperCompanies A tiempo completo

    Overview LI-onsite (converted content) - At CooperSurgical, we are currently looking to recruit a Regulatory Affairs Specialist to join our Global Regulatory Affairs team. This role focuses primarily on the US (FDA), Canada (Health Canada) and Australia (TGA) markets, ensuring compliance and supporting submissions that enable patients and healthcare...


  • Barcelona, España CooperCompanies A tiempo completo

    Overview LI-onsite (converted content) - At CooperSurgical, we are currently looking to recruit a Regulatory Affairs Specialist to join our Global Regulatory Affairs team. This role focuses primarily on the US (FDA), Canada (Health Canada) and Australia (TGA) markets, ensuring compliance and supporting submissions that enable patients and healthcare...


  • Barcelona, España ESTEVE A tiempo completo

    A pharmaceutical company in Barcelona is seeking a Regulatory Affairs Specialist to manage the regulatory lifecycle of US FDA-approved products. The role includes preparing FDA documentation, maintaining compliance, and collaborating with cross-functional teams. Candidates should have a Bachelor's degree in a relevant field and 3–5 years of experience in...


  • Barcelona, España Symrise AG A tiempo completo

    Symrise is a global supplier of fragrances and flavors, cosmetic active ingredients, and functional ingredients. Its customers include manufacturers of perfumes, cosmetics, food and beverages, the pharmaceutical industry, and producers of dietary supplements and pet food. With sales of approximately €5 billion in fiscal year 2024, the company is one of the...


  • Barcelona, España Grouper Technology A tiempo completo

    Regulatory Affairs Specialist (Full-time, Permanent)Prinova is a leading global supplier of ingredients and premix manufacturing solutions for the food, beverage and nutrition industries. Prinova holds strategic stocks in 35+ centres around the world to ensure continuity of supply and has liquid and dry premix manufacturing facilities in the UK, China and...


  • Barcelona, España Grouper Technology A tiempo completo

    Regulatory Affairs Specialist (Full-time, Permanent) Prinova is a leading global supplier of ingredients and premix manufacturing solutions for the food, beverage and nutrition industries. Prinova holds strategic stocks in 35+ centres around the world to ensure continuity of supply and has liquid and dry premix manufacturing facilities in the UK, China and...


  • Barcelona, Barcelona, España Prinova Europe A tiempo completo

    Regulatory Affairs Specialist (Full-time, Permanent)Unlock your potential with PrinovaWe are Prinova, a leading global supplier of ingredients and premix manufacturing solutions and trusted by the world's best-known food, beverage, and nutrition brands.Part of the NAGASE Group, our expertise lies in Ingredient Distribution, Manufacturing Solutions, and...