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6 results for expert-regulatory-affairs jobs in East Flanders within a 30 km radius
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Als Regulatory Affairs Officer ben je verantwoordelijk voor het waarborgen van de naleving van alle Europese en nationale regelgeving met betrekking tot geneesmiddelen gedurende hun volledige levenscyclus. • Je hebt minstens 2 jaar ervaring binnen Regulatory Affairs in de farmaceutische sector
Als Regulatory Affairs Officer ben je verantwoordelijk voor het waarborgen van de naleving van alle Europese en nationale regelgeving met betrekking tot geneesmiddelen gedurende hun volledige levenscyclus. • Je hebt minstens 2 jaar ervaring binnen Regulatory Affairs in de farmaceutische sector
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No match yet? There are 5 more jobs that could match your search
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Being a resident in Belgium for the last 5 consecutive years and having familiarity with current and historical business, media, sport, news, social media, and cultural affairs in Belgium
Being a resident in Belgium for the last 5 consecutive years and having familiarity with current and historical business, media, sport, news, social media, and cultural affairs in Belgium
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You will contribute to international roll-outs, compliance initiatives, legal and regulatory changes, treasury implementations and continuous improvement projects.
You will contribute to international roll-outs, compliance initiatives, legal and regulatory changes, treasury implementations and continuous improvement projects.
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Ensure products are scalable, manufacturable, and compliant with quality and regulatory requirements.
Ensure products are scalable, manufacturable, and compliant with quality and regulatory requirements.
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This role ensures compliance with food safety standards, regulatory requirements, and company policies while striving to improve operational efficiency and maintaining a safe, hygienic, and productive environment. * Ensure adherence to sanitation standard operating procedures (SSOPs) and food safety protocols, including Good Manufacturing Practices (GMP), Hazard Analysis Critical Control Points (HACCP), and other relevant regulatory guidelines. * Regulatory Compliance: Ensure the facility complies with all local, state, and federal regulations, including OSHA, FDA, USDA, and EPA standards. Maintain records related to sanitation activities, cleaning logs, and other documentation as required by regulatory authorities. Ensure that cleaning chemicals and supplies are stored, handled, and disposed of accor
This role ensures compliance with food safety standards, regulatory requirements, and company policies while striving to improve operational efficiency and maintaining a safe, hygienic, and productive environment. * Ensure adherence to sanitation standard operating procedures (SSOPs) and food safety protocols, including Good Manufacturing Practices (GMP), Hazard Analysis Critical Control Points (HACCP), and other relevant regulatory guidelines. * Regulatory Compliance: Ensure the facility complies with all local, state, and federal regulations, including OSHA, FDA, USDA, and EPA standards. Maintain records related to sanitation activities, cleaning logs, and other documentation as required by regulatory authorities. Ensure that cleaning chemicals and supplies are stored, handled, and disposed of accor
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The Business Unit specializes in asbestos-related services, supporting customers across Belgium with laboratory analysis, inspections, and regulatory compliance.
The Business Unit specializes in asbestos-related services, supporting customers across Belgium with laboratory analysis, inspections, and regulatory compliance.
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4 exact matches jobs are outside your preferred location
European Government Affairs – Political Affairs Director - Microsoft's European Government Affairs (EGA) team serves as the company's primary interface with the European institutions, national governments, and key stakeholders across the region. As Europe navigates an increasingly complex political and regulatory environment, effective engagement with the European Commission, European Parliament, and Council of the European Union is critical to Microsoft's success. The EGA team in Brussels is seeking a Political Affairs Director to strengthen Microsoft's engagement with the European institutions, especially the European Commission and Council of the European Union, by providing strategic political counsel, facilitating senior-level access, and advancing relationships with key decision
European Government Affairs – Political Affairs Director - Microsoft's European Government Affairs (EGA) team serves as the company's primary interface with the European institutions, national governments, and key stakeholders across the region. As Europe navigates an increasingly complex political and regulatory environment, effective engagement with the European Commission, European Parliament, and Council of the European Union is critical to Microsoft's success. The EGA team in Brussels is seeking a Political Affairs Director to strengthen Microsoft's engagement with the European institutions, especially the European Commission and Council of the European Union, by providing strategic political counsel, facilitating senior-level access, and advancing relationships with key decision
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Collaborer avec les équipes , QA, QC, Regulatory Affairs, MSAT, Manufacturing et Process afin de garantir l'avancement du projet. Dans le cadre d'un projet de développement pharmaceutique en phase avancée, proche de la commercialisation, vous apporterez un support scientifique et projet à un expert technique (SME/Project Lead).
Collaborer avec les équipes , QA, QC, Regulatory Affairs, MSAT, Manufacturing et Process afin de garantir l'avancement du projet. Dans le cadre d'un projet de développement pharmaceutique en phase avancée, proche de la commercialisation, vous apporterez un support scientifique et projet à un expert technique (SME/Project Lead).
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Through certification, auditing, training and assurance services, we support companies in building trust, enhancing quality, ensuring regulatory compliance and driving continuous improvement across their operations. Our experts deliver a wide range of standard and non-standard tests on medical devices and certify them through our notified bodies. * Collaborate with SGS Notified Bodies, technical experts, and global teams to ensure access to the required capabilities and expertise. The successful candidate is an experienced Medical Devices business leader who combines strong Medical Devices industry credibility and regulatory understanding with commercial judgement, customer leadership and P&L accountability. Deeper technical or regulatory expertise is an advantage, not a prerequisite.
Through certification, auditing, training and assurance services, we support companies in building trust, enhancing quality, ensuring regulatory compliance and driving continuous improvement across their operations. Our experts deliver a wide range of standard and non-standard tests on medical devices and certify them through our notified bodies. * Collaborate with SGS Notified Bodies, technical experts, and global teams to ensure access to the required capabilities and expertise. The successful candidate is an experienced Medical Devices business leader who combines strong Medical Devices industry credibility and regulatory understanding with commercial judgement, customer leadership and P&L accountability. Deeper technical or regulatory expertise is an advantage, not a prerequisite.
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Market Intelligence: Monitor industry trends, activity, and regulatory changes to position SGS as a trusted advisor.
Market Intelligence: Monitor industry trends, activity, and regulatory changes to position SGS as a trusted advisor.