Key Skills

Job Description

Quality & Regulatory Manager Vital20 | Go-Keto | Swiss Point of Care Leimuiden | Full-time Help build Quality within a growing international organisation Do you have several years of experience in Quality or Regulatory, for example within food, food supplements, private label, FMCG, retail or consumer healthcare, and are you ready for a broader role with more responsibility? At Vital20, you will become the internal owner of our Quality, Regulatory and Compliance processes. You will make sure that products, documentation, registrations and quality systems are not only correct, but also properly followed up and completed. We are not looking for a senior Quality Director or a purely theoretical Regulatory specialist. We are looking for someone who is accurate and structured, but above all practical, hands-on and able to take ownership. About Vital20 Vital20 operates across food, supplements, preventive health and medical diagnostics, including through the Go-Keto and Swiss Point of Care brands. We develop and sell products across several European markets and work closely with suppliers, manufacturers, external specialists and international partners. We are a small and dynamic team with short communication lines, a high level of personal responsibility and plenty of room to move quickly. As we continue to grow, Quality & Regulatory is becoming increasingly important. We are therefore bringing the day-to-day ownership of these processes firmly in-house. What will you do? As Quality & Regulatory Manager, you will ensure that our products and processes remain complete, up to date and compliant. Your Responsibilities Will Include managing product and supplier files, specifications and certificates; reviewing and approving labels, claims and packaging; coordinating product registrations and notifications across European markets; ensuring Food and Food Supplements compliance; managing supplier quality, deviations and CAPAs; supporting complaints, recalls and traceability processes; preparing for and following up on audits; maintaining and further developing our Quality Management Systems; monitoring packaging and environmental compliance, including EPR and WEEE; working closely with external Quality and Regulatory specialists. External experts will remain available for specialist topics. You will make sure internally that information is provided, actions are followed up, deadlines are met and dossiers are closed. ISO 22000 & Medical Devices Vital20 is further developing its ISO 22000 Food Safety Management System. You will play an active role in this process and gradually take internal ownership of areas including HACCP, procedures, CAPA, audits, supplier quality, traceability and management review. Through Swiss Point of Care, we are also active in Medical Devices and IVD and work with ISO 13485. You do not need to be a Medical Device specialist from day one. However, we expect you to be willing to develop your knowledge of ISO 13485, IVDR and our responsibilities as importer and distributor. Involved from the start Quality is not only involved once a package is ready for print. Where relevant, you will be involved early in product development and review areas such as specifications, ingredients, claims, mandatory information, labels and packaging. One Important Principle Is No Quality approval = No print. At the same time, we are not looking for someone whose role is simply to say no. We want someone who identifies the issue, understands the requirements and then provides practical options and a clear recommendation. Who are we looking for? You preferably have several years of relevant experience within areas such as: Food; Food Supplements; Private Label; FMCG; Retail Quality; Consumer Healthcare. In Addition, You work accurately and in a structured way; are hands-on and independent; are strong in follow-up and deadline management; take ownership of dossiers and make sure actions are completed; are comfortable dealing with suppliers and external specialists; are pragmatic and solution-oriented; can manage multiple products and dossiers at the same time; are willing to learn new regulatory areas; have professional proficiency in both Dutch and English. Experience with ISO 22000, HACCP, product registrations, supplier quality, audits, food supplements or CAPA is a strong advantage. Experience with Medical Devices, ISO 13485 or IVDR is welcome, but not required What do we offer? A broad Quality & Regulatory role with significant personal responsibility. The opportunity to further build Quality within Vital20. A varied scope across Food, Supplements and Medical Devices. Close collaboration with suppliers, specialists and internal teams. Short communication lines and fast decision-making within a small team. Direct collaboration with management, Purchasing, Marketing and Operations. Opportunities to further develop your knowledge of ISO 22000, ISO 13485 and international regulatory topics. A salary based on your knowledge and experience. Based in Leimuiden. Full-time position. A maximum of one work-from-home day per week. Interested? Do you have experience within Quality or Regulatory and are you ready for a broad, independent role in which you can take real ownership of processes and dossiers? We would be happy to hear from you. Please Send Your CV Or LinkedIn Profile To Ben Nordemann [email protected] +31 6 47 80 83 82 Vital20 | Go-Keto | Swiss Point of Care Sign Up Now Be the first to receive freshly new offers, recipes and tips & tricks! Sign up for our newsletter and receive € 5.- discount on your next order! E-mail Vital20 B.V. 3404 LJ IJsselstein Netherlands Chamber of commerce: 55.936.091 VAT ID. NL851914603B01 EORI: NL851914603 Brands Go-Keto Live Fatt Palmini About About Us Blog Vital 20 Wholesale Reviews Loyalty & Rewards Careers Internships Affiliate Policies Return Policy Shipping Policy Privacy Policy Terms of Service Legal Notice We Can Help Contact Us My Account My Wishlist Returns & Withdrawal Country Language American Express Apple Pay Bancontact Google Pay iDEAL Wero Klarna Maestro Mastercard MobilePay PayPal Shop Pay Union Pay Visa © 2026 - Vital20 - All rights reserved The information on this site is for educational purposes only and is not medical advice.

Core Responsibilities

The manager will own the internal Quality, Regulatory, and Compliance processes across food, supplements, and medical devices. Key duties include managing supplier files, approving labels, coordinating European product registrations, and maintaining Quality Management Systems.

Requirements

Candidates should have several years of experience in Quality or Regulatory roles within FMCG, food, or healthcare sectors. Proficiency in Dutch and English is required, along with a practical, hands-on approach to compliance and a willingness to learn ISO 13485 and IVDR.

Benefits

• Salary based on knowledge and experience
• Professional development in ISO 22000 and ISO 13485
• Opportunity to build quality processes within a growing organization