Hire the best Regulatory Compliance Freelancers in Ireland
Check out Regulatory Compliance Freelancers in Ireland with the skills you need for your next job.
- $90 hourly
- 5.0/5
- (7 jobs)
⭐⭐⭐⭐⭐ As a dedicated Security Certification Consultant, I specialize in guiding SaaS companies through the nuanced path to achieving SOC 2, ISO 27001, and other secuirty certifications, with a specialized focus on leveraging the Vanta platform. With my extensive background in cybersecurity, particularly within cloud environments like AWS, Azure and moreso GCP these days, I am adept at crafting tailored solutions that align with SaaS operational models and security needs. Navigating the cloud's unique security challenges is second nature to me. I offer deep expertise in cloud security controls, data protection standards, and compliance frameworks that are crucial for SaaS platforms looking to excel in today's digital landscape. My credentials as an ISO 27001 Lead Implementor and Certified VANTA Partner underscore my ability to integrate best practices into your security strategy effectively. In a recent standout project, an ambitious French-based SaaS startup approached me with a problem I hear over and over. They had a big enterprise client ready to sign up, but they needed to be ISO27001 certified before that would happen. I assured them that achieving ISO27001 certification within a 12-week timeline was achievable. This fast-paced success was enabled through the strategic use of the Vanta platform, facilitating seamless integration and automation of compliance processes. Under my guidance, the client’s development team focused on required infrastructure changes and Vanta integrations while I focused on drafting critical policy documents and overseeing the documentation necessary for certification. Throughout the process, I managed the project using my 12-week certification roadmap, which I have refined continuously over many certification projects. This approach expedited the certification process and ensured that all security measures were robust and tailored to the specific needs of a dynamic SaaS environment. By aligning the client’s technical enhancements with strategic policy development, we achieved compliance efficiently and effectively, allowing the client to onboard with a flagship client critical to their growth. Key Services: ✅Security Certification Planning and Execution for SaaS Companies ✅Cloud Security Optimization for AWS and Azure ✅Compliance Automation using Vanta ✅Strategic Risk Assessments and Cloud Security Audits Why Choose Me? ✅Profound understanding of SaaS operational and security needs ✅Expert navigation of cloud infrastructures and compliance requirements ✅Efficient, structured delivery with proven SaaS-specific outcomes ✅Continuous engagement and transparency via Slack or Teams ✅ Expert in deploying Vanta for automated compliance and certification ✅ Specialized in adapting Vanta to diverse SaaS frameworks ✅ Conduct detailed assessments to identify compliance needs and gaps ✅ Utilize cutting-edge tools for seamless integration and monitoring ✅ Offer actionable insights and strategies to maintain continuous compliance ✅ Ensure data protection and security practices exceed industry standards ✅ Assist with achieving certifications such as SOC 2, ISO 27001, and GDPR compliance ✅ Collaborative approach with IT and development teams to customize solutions ✅ Provide comprehensive training and support to client teams ✅ Dedicated to simplifying compliance through technology ✅ Commitment to upholding the highest standards of data integrity and security ✅ Foster a proactive compliance culture within organizations I am here to deliver robust and adaptive solutions if you're looking for an expert to deploy Vanta and efficiently guide you through the compliance and certification process. Let's work together to ensure your services are secure, compliant, and certified, setting you apart from competitors in your industry.
Regulatory Compliance
PCIPCI DSSSecurity Policies & Procedures DocumentationSaaSData ProtectionPrivacy LawISO 27001Intellectual Property LawData PrivacyContract DraftingPenetration TestingLegal ResearchPolicy WritingCompliance ConsultationInformation SecurityContract LawLegalLegal ConsultingGDPRCompliance - $89 hourly
- 4.7/5
- (22 jobs)
My name is Rebecca, and I am an experienced, results-driven Regulatory Affairs Specialist. With over 6 years of hands-on regulatory expertise across a range of industries—most notably the medical device sector—I specialise in ensuring that companies achieve unparalleled compliance while navigating the complexities of global regulations. My mission is simple: to take the burden of regulatory requirements off your shoulders and drive your success in any regulated market. Why Work With Me? I combine exceptional technical knowledge, a passion for the intricacies of regulatory law, and a proven ability to adapt to any regulated industry. Whether you need support in medical devices, pharma, biotechnology, or other industries requiring rigorous compliance, I have the expertise to deliver solutions tailored to your needs. My clients span start-ups, established corporations, and global market leaders—all of whom trust me to lead them through the challenges of compliance and quality assurance. Key Highlights of My Expertise: Global Regulatory Compliance: Proficient in FDA submissions, EU MDR compliance, CE marking, ISO certifications, and more. Extensive experience in regulated industries, including medical devices, pharmaceuticals, consumer goods, and software as a medical device (SaMD). Skilled in adapting to the unique demands of each regulatory framework to ensure seamless product launches. Quality Management Systems (QMS): Design, implementation, and auditing of ISO 13485-compliant QMS for medical devices and other regulated industries. Internal auditing expertise, ensuring the highest standards for safety, risk management, and post-market surveillance. Experience with CAPA (Corrective and Preventive Actions) and MDSAP standards for quality excellence. Technical and Regulatory Writing: Creation of FDA-ready technical documentation, Declarations of Conformity, Instructions for Use (IFUs), and product labelling. Writing marketing materials, blogs, and whitepapers to communicate complex compliance topics clearly and effectively. Developed 100+ pages of regulatory documentation for AdvaCare Pharma, leading to my appointment as a Board Member of Medical Advisors. Adaptability Across Regulated Markets: My expertise translates seamlessly to consumer products, biotech, cosmetics, environmental regulations, and more. Well-versed in providing compliance solutions tailored to specific industries' needs and timelines. My Passion & Mission: Compliance is more than a requirement—it’s an opportunity to build trust, protect consumers, and drive innovation. I am deeply passionate about regulatory affairs because I know that meticulous adherence to standards doesn’t just ensure safety—it opens doors to global markets, ensures sustainable growth, and builds long-term reputations. As an active member of TOPRA and RAPS, I stay at the forefront of industry developments and emerging regulations. This allows me to bring cutting-edge insights and proactive strategies to every project I undertake. Certifications & Qualifications: ISO 13485:2016 Lead Auditor – British Standards Institute (BSI). MDSAP Internal Quality Auditor Certification. Masters in Medical Device Regulatory Affairs (MSc) with First Class Honors. Extensive training in FDA CFR Part 820, IEC 60601-1, and other critical compliance standards. Industries I Support: Medical Devices: From Class I to III, including SaMD (Software as a Medical Device). Pharmaceuticals: Regulatory documentation, quality systems, and compliance guidance. Consumer Goods: Adherence to safety regulations and quality standards. Biotechnology: Compliance strategies for innovative and cutting-edge technologies. Cosmetics and Personal Care: Navigating global regulations, including EU and FDA requirements. What Clients Say About Me: "Rebecca is a regulatory affairs specialist with years of experience in the medical device sector. Her expertise spans regulatory compliance in major markets, including the US, EU and Asia, and the implementation of Quality Management Systems (QMS) compliant with global standards. Rebecca excels in translating complex technical information into clear, accessible content. As an active member in TOPRA & RAPS and position as Lead Auditor, she has experience in every aspect of regulatory affairs and quality assurance. Rebecca’s contributions to enhancing medical device compliance underscores her exceptional ability in providing critical medical information effectively. " – AdvaCare Pharma Let’s Work Together: If you’re looking for a trusted partner who will not only ensure compliance but also provide strategic insight, I’m here to help. Whether you need help with FDA submissions, ISO certifications, regulatory audits, or compliance content, I’ll bring clarity, precision, and results to your project. Let’s connect to discuss how I can contribute to your success! Rebecca
Regulatory Compliance
SEO ContentBlog WritingContent WritingTechnical WritingArticle WritingCopywritingSEO WritingPharmaceutical IndustryMedical WritingQuality AuditISO 9001Quality Management SystemMedical DeviceBlog Content - $100 hourly
- 5.0/5
- (2 jobs)
specializing in regulatory licensing across the globe, with a focus on sectors such as E-Money (EMI), Payments (PI), MiFID, Cryptocurrency, and Virtual Asset Service Providers (VASPs). My extensive experience includes leading regulatory license applications and obtaining authorization approval, navigating complex regulatory landscapes, and implementing strategic capital risk management practices. Key Achievements and Experience: Regulatory Competency: Approved by regulators for roles such as Chief Executive Officer, Chief Risk Officer, MLRO, and Head of Compliance. I have successfully led the compliance and risk departments of companies pre and post-authorization and dealt with global regulators like the Central Bank of Ireland, AMF (France), FCA (UK), DFSA (Dubai), OEM (Italy), and SEC (USA). Leadership: Proven leader in building and scaling compliance & risk teams up to 30 members, and currently leading a business of 70 people. Strategic Implementation: Successfully implemented comprehensive controls that are justifiable to regulators and resulted in substantial cost savings in the millions of Euros for the current organization. Efficiency & Automation: Leveraged my understanding of the regulatory landscape to bring efficiency and automation within building in-house governance, risk, and compliance solutions. Education & Memberships: Advanced Risk Management within Banking Services, Master's Level 9, University College of Dublin (2022) Professional Diploma in Compliance, Degree Level 7, University College of Dublin (2022) Member, Association of Compliance Officers in Ireland Member, Institute of Directors Summary: With an in-depth understanding of high-risk sectors such as cryptocurrency and a proven record in leading regulatory license applications in multiple countries, I am well-equipped to meet the regulatory licensing needs of clients. I look forward to leveraging my skills and expertise to bring value to your organization.
Regulatory Compliance
eMoney Advisor emXCompliance PlanManagement SkillsLegalConsumer ProtectionRisk ManagementGovernment Reporting ComplianceCompliance TestingComplianceInternal ControlAnti-Money LaunderingBusiness with 10-99 EmployeesCompliance ConsultationGDPR - $30 hourly
- 0.0/5
- (0 jobs)
I am an experienced pharmaceutical professional specializing in regulatory affairs, quality control (QC), quality assurance (QA), scientific writing, and data analysis. With hands-on experience in pharmaceutical companies, I help clients navigate complex regulatory requirements, ensure compliance, and create high-quality documentation. My expertise includes preparing regulatory submissions, conducting audits, ensuring GMP compliance, and analyzing scientific data. I excel at crafting clear, concise reports and documents, including clinical trial reports, lab reports, and standard operating procedures (SOPs). I am committed to delivering accurate, timely work and ensuring full compliance with industry standards. Let’s collaborate to streamline your project.
Regulatory Compliance
Environmental ScienceChromatographyData EntryData AnalysisPharmaceuticalsPharmaceutical IndustryLab ReportReport WritingAdministrative SupportScientific & Technical ServicesQuality ControlQuality AssuranceChemistryScience Want to browse more freelancers?
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