Regulatory Affairs Specialist

hace 4 días

Barcelona, España Prinova Global 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. With strategic stocks in 35+ centres around the world and manufacturing facilities in the UK, China and the USA, Prinova’s premix business is underpinned by over 40 years of experience in ingredient sourcing and distribution.Key ResponsibilitiesProvide 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.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 (e.g., 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, ensuring 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.Assist in the management of crises and incidents as part of the management team.What’s in it for youPersonal growth, including training and development opportunitiesDiscretionary bonusCompany eventsTravelQualifications5+ years of technical or regulatory experience in food, feed, fine chemicals, pharmaceutical ingredient and/or chemical distribution.Highly analytical and organised with keen attention to detail.Ability to identify problems and provide systematic solutions.Ability 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.High level of business English is essential.Self‑motivated.Strong administration skills on Microsoft Office, Windows.How to ApplyWe would love to hear from you. Submit your CV by clicking apply.#J-18808-Ljbffr

  • Regulatory Affairs Specialist

    hace 12 horas

    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...

  • Regulatory Affairs Specialist

    hace 16 horas

    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...

  • Regulatory Affairs Senior Specialist

    hace 2 días

    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...

  • Regulatory Affairs Senior Specialist

    hace 3 días

    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...

  • Regulatory Affairs Specialist: FDA Submissions

    hace 12 horas

    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...

  • Regulatory Affairs Specialist

    hace 4 días

    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...

  • Regulatory Affairs Specialist

    hace 14 horas

    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...

  • Regulatory Affairs Specialist

    hace 4 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...

  • Regulatory Affairs Specialist

    hace 1 semana

    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...

  • Senior CMC Regulatory Affairs Specialist

    hace 4 días

    Barcelona, España Project Delivery Partners Pte Ltd A tiempo completo

    A leading consulting firm in Barcelona seeks a dedicated Senior CMC RA Specialist. This on-site role focuses on ensuring regulatory compliance in Chemistry, Manufacturing, and Controls (CMC) documentation. The ideal candidate has over 10 years of experience in Regulatory Affairs within the pharmaceutical industry, strong knowledge of GMP and ICH guidelines,...