Regulatory Affairs Specialist

hace 1 semana


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 detail.  Must be able to identify problems and provide a systematic solution. 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, Barcelona, España Inter Regulatory A tiempo completo

    Regulatory Affairs Associate (Medicines)Location:Barcelona, Spain (Hybrid – Barcelona Health Hub)Company:Inter RegulatoryEmployment Type:Full-timeAbout the roleInter Regulatory is expanding its European Regulatory Affairs team and is seeking aRegulatory Affairs Associate (Medicines)to join our consultancy based inBarcelona, primarily working from...


  • Barcelona, España Inter Regulatory A tiempo completo

    Regulatory Affairs Associate (Medicines) Company: Inter RegulatoryEmployment Type: Full-timeAbout the role Inter Regulatory is expanding its European Regulatory Affairs team and is seeking a Regulatory Affairs Associate (Medicines) to join our consultancy based in Barcelona , primarily working from the Barcelona Health Hub .This role is suited to a...


  • Barcelona, España Inter Regulatory A tiempo completo

    A growing regulatory consultancy in Barcelona is seeking a Regulatory Affairs Associate with 3-5 years of experience in pharmaceutical Regulatory Affairs. The role involves authoring and managing regulatory dossiers, handling CMC documentation, and supporting US regulatory applications. Candidates should have a scientific degree and be fluent in English and...


  • 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

    #LI-onsite 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 professionals to access our innovative...


  • Barcelona, España Solo Talento | RH Soluciones A tiempo completo

    Una compañía internacional del sector nutracéutico busca un Regulatory Affairs Specialist para su oficina en Barcelona. Este puesto se centra en garantizar el cumplimiento normativo global, apoyando a las operaciones comerciales y de I+D. El candidato ideal debe tener al menos 4 años de experiencia en Regulatory Affairs en nutracéuticos y un sólido...


  • Barcelona, España ESTEVE A tiempo completo

    Join to apply for the Regulatory Affairs Specialist role at ESTEVE . Overview Manage 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, España Solo Talento | RH Soluciones A tiempo completo

    Compañía internacional del sector de nutracéuticos y suplementos dietéticos busca incorporar un Regulatory Affairs Specialist para su sede en Barcelona, con foco en mercados internacionales.Este puesto es clave para garantizar el cumplimiento normativo global, dar soporte a las operaciones comerciales y de I+D, y minimizar riesgos regulatorios en todos...


  • barcelona, España Solo Talento | RH Soluciones A tiempo completo

    Compañía internacional del sector de nutracéuticos y suplementos dietéticos busca incorporar un Regulatory Affairs Specialist para su sede en Barcelona, con foco en mercados internacionales. Este puesto es clave para garantizar el cumplimiento normativo global, dar soporte a las operaciones comerciales y de I+D, y minimizar riesgos regulatorios en todos...

  • MedTech Quality

    hace 1 día


    Barcelona, España Ersilia A tiempo completo

    A medical technology company in Barcelona is looking for a Quality & Regulatory Affairs Specialist to enhance quality and regulatory processes. This role involves preparing regulatory submissions, conducting audits, and collaborating on compliance initiatives. Candidates should have a Bachelor’s degree in a relevant field and 2 years of experience in the...