Selected: đ Compliance.
Selected: đźđč Italy â Remote.
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Selected: đ Date Added.
đ„ 20 hours ago
Senior GRC Engineer securing Isovalentâs Hypershield solution through risk management, compliance automation, and DevSecOps. Supporting Ciscoâs cloud-native networking, security, and observability products.
đ Yesterday
Clinical research manager leading study start-up and regulatory affairs for Ergomedâs rare disease and oncology trials. Overseeing regulatory strategy, site activation, documents, budgets, and global project delivery.
đ Yesterday
CMC regulatory director leading Thermo Fisher Scientificâs EMEA FSP teams, client strategy, resourcing, and delivery. Supporting business development, compliance, budgeting, and process improvement.
đ 6 days ago
Regulatory Affairs Manager leading clinical trial regulatory strategy, submissions, and compliance for pharmaceutical product development. Driving cross-functional execution, client guidance, budgets, and regulatory decisions.
đ Belgium, Italy, +3 more countries â Remote
â° Full Time
đ Senior
đŽ Lead
đ Compliance
đ» Ghost score 10%
đ November 4
CMC regulatory director leading Thermo Fisher Scientificâs EMEA FSP teams and client delivery. Advising on regulatory strategy, resource planning, budgets, and business development.
đ November 4
Regulatory intelligence manager monitoring global requirements and advising pharmaceutical and biotech clients. Leading submissions, precedent research, stakeholder alignment, and strategic regulatory guidance.
đ United Kingdom, Belgium, +3 more countries â Remote
â° Full Time
đ Senior
đŽ Lead
đ Compliance
đ» Ghost score 10%
đ November 4
Senior regulatory specialist managing clinical-trial registrations, results postings, and CTIS redactions. Supporting pharmaceutical and biotech clients with global regulatory strategy and compliance.
đ November 3
Senior Regulatory Affairs Manager guiding CMC submissions, variation strategies, and regulatory responses for Parexelâs pharmaceutical clients. Coordinating global affiliates and manufacturing sites across European locations.
đ United Kingdom, Croatia, +7 more countries â Remote
đ° Venture Round on 1990-01
â° Full Time
đ Senior
đ Compliance
đŹđ§ UK Skilled Worker Visa Sponsor
đ» Ghost score 10%
đ November 2
Senior QA/RA specialist supporting Henry Scheinâs EMEA medical-device quality and regulatory operations. Maintaining QMS, CAPA, audits, compliance, and regulatory initiatives across multiple countries.
đ October 12
Compliance Officer owning EEA and UK e-money regulatory workstreams for a global crypto-payments fintech. Drafting authorisation materials, safeguarding frameworks, and post-licence compliance evidence.
đȘđș Europe â Remote
âł Contract/Temporary
đĄ Mid-level
đ Senior
đ Compliance
đ» Ghost score 22%
đ October 5
Compliance Analyst investigating blockchain transactions and complex AML cases for OKX, a leading crypto exchange and wallet developer. Assessing illicit activity, regulatory risk, and transaction-monitoring controls.
đ September 22
Senior Internal Audit manager developing GRC advisory and transformation solutions for banks and financial institutions at Prometeia. Leading methodologies, analytics, AI-enabled auditing and client delivery.
đ September 18
Regulatory Affairs Consultant managing post-approval CMC submissions for Parexel's clinical development and regulatory services. Supporting vaccine and biological-product compliance across European locations.
đ Italy, Croatia, +5 more countries â Remote
đ° Venture Round on 1990-01
â° Full Time
đĄ Mid-level
đ Senior
đ Compliance
đ» Ghost score 29%
đ September 4
Application Security specialist auditing CVE tasks for Meridialâs AI training systems. Evaluating vulnerabilities, exploits, mitigations, and technical accuracy.
đ Anywhere in the World
đ” $70 - $100 / hour
đ„ Funding within the last year
đ° $100M Series unknown on 2025-10
âł Contract/Temporary
đĄ Mid-level
đ Senior
đ Compliance
đ» Ghost score 3%
Likely ghost job
đ August 27
Likely ghost job
Regulatory Affairs Consultant leading IVD regulatory strategy, technical documentation, and health-authority interactions. Supporting Parexelâs clinical development and regulatory consulting solutions across European locations.
đ Italy, Croatia, +3 more countries â Remote
đ° Venture Round on 1990-01
â° Full Time
đĄ Mid-level
đ Senior
đ Compliance
đ» Ghost score 61%
đ August 27
Senior Regulatory Affairs Associate managing post-approval CMC submissions for Parexelâs pharmaceutical clients. Coordinating regulatory documentation for biologics and vaccines across European locations.
đ Italy, Croatia, +5 more countries â Remote
đ° Venture Round on 1990-01
â° Full Time
đ Senior
đ Compliance
đ» Ghost score 51%
đ July 15
Senior Regulatory Affairs Associate managing CMC post-approval submissions for Parexelâs pharmaceutical clients. Developing regulatory strategies for biologics and vaccines across European locations.
đ Poland, Croatia, +5 more countries â Remote
đ° Venture Round on 1990-01
â° Full Time
đ Senior
đ Compliance
đ» Ghost score 55%
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