Ocupaciones

Oficiales de cumplimiento

1929 habilidades

Preguntar a IA

1929 habilidades

Ocupaciones

Oficiales de cumplimiento

1929 habilidades

Preguntar a IA

1929 habilidades

Ocupaciones

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Documentos

Customs Trade Compliance

海关文件、关税分类、关税优化、受限方筛查以及多司法管辖区法规合规的编码化专业知识。由拥有15年以上经验的贸易合规专家提供。包括HS分类逻辑、Incoterms应用、自贸协定利用以及罚款减免。适用于处理海关清关、关税分类、贸易合规、进出口文件或关税优化时使用。license: Apache-2.0

affaan-m160.3k

Ventas y Marketing

Codified expertise for customs documentation, tariff classification, duty optimization, restricted party screening, and regulatory compliance across multiple jurisdictions. Informed by trade compliance specialists with 15+ years experience. Includes HS classification logic, Incoterms application, FTA utilization, and penalty mitigation. Use when handling customs clearance, tariff classification, trade compliance, import/export documentation, or duty optimization.

affaan-m160.3k

Ventas y Marketing

Quality & Non-Conformance Management

Codified expertise for quality control, non-conformance investigation, root cause analysis, corrective action, and supplier quality management in regulated manufacturing. Informed by quality engineers with 15+ years experience across FDA, IATF 16949, and AS9100 environments. Includes NCR lifecycle management, CAPA systems, SPC interpretation, and audit methodology. Use when investigating non-conformances, performing root cause analysis, managing CAPAs, interpreting SPC data, or handling supplier quality issues.

affaan-m160.3k

Calidad de Código

Quality Nonconformance

为受监管制造业中的质量控制、不合格调查、根本原因分析、纠正措施和供应商质量管理提供编码化专业知识。基于在FDA、IATF 16949和AS9100环境中拥有15年以上经验的质量工程师的见解。包括不合格报告生命周期管理、纠正与预防措施系统、统计过程控制解释和审核方法。适用于调查不合格、进行根本原因分析、管理纠正与预防措施、解释统计过程控制数据或处理供应商质量问题。license: Apache-2.0

affaan-m160.3k

Ventas y Marketing

Gdpr Data Handling

Practical implementation guide for GDPR-compliant data processing, consent management, and privacy controls.

sickn3333.8k

Pagos

Pci Compliance

Master PCI DSS (Payment Card Industry Data Security Standard) compliance for secure payment processing and handling of cardholder data.

sickn3333.8k

Documentos

Customs Trade Compliance

Codified expertise for customs documentation, tariff classification, duty optimisation, restricted party screening, and regulatory compliance across multiple jurisdictions.

sickn3333.8k

Seguridad

Fda Food Safety Auditor

Expert AI auditor for FDA Food Safety (FSMA), HACCP, and PCQI compliance. Reviews food facility records and preventive controls.

sickn3333.8k

Finanzas e Inversión

Data Privacy Compliance

Data privacy and regulatory compliance specialist for GDPR, CCPA, HIPAA, and international data protection laws. Use when implementing privacy controls, conducting data protection impact assessments, ensuring regulatory compliance, or managing data subject rights. Expert in consent management, data minimization, and privacy-by-design principles.

davila724.7k

Seguridad

Compliance

Compliance expert for SOC 2, GDPR, HIPAA, PCI-DSS, and security frameworks

RightNow-AI16.8k

Ventas y Marketing

Quality Manager Qmr

Senior Quality Manager Responsible Person (QMR) for HealthTech and MedTech companies. Provides quality system governance, management review leadership, regulatory compliance oversight, and quality performance monitoring per ISO 13485 Clause 5.5.2.

alirezarezvani11.7k

Gestión de Proyectos

Capa Officer

CAPA system management for medical device QMS. Covers root cause analysis, corrective action planning, effectiveness verification, and CAPA metrics. Use for CAPA investigations, 5-Why analysis, fishbone diagrams, root cause determination, corrective action tracking, effectiveness verification, or CAPA program optimization.

alirezarezvani11.7k

Inmobiliaria y Legal

Mdr 745 Specialist

EU MDR 2017/745 compliance specialist for medical device classification, technical documentation, clinical evidence, and post-market surveillance. Covers Annex VIII classification rules, Annex II/III technical files, Annex XIV clinical evaluation, and EUDAMED integration.

alirezarezvani11.7k

Seguridad

Gdpr Dsgvo Expert

GDPR and German DSGVO compliance automation. Scans codebases for privacy risks, generates DPIA documentation, tracks data subject rights requests. Use for GDPR compliance assessments, privacy audits, data protection planning, DPIA generation, and data subject rights management.

alirezarezvani11.7k

Inmobiliaria y Legal

Quality Documentation Manager

Document control system management for medical device QMS. Covers document numbering, version control, change management, and 21 CFR Part 11 compliance. Use for document control procedures, change control workflow, document numbering, version management, electronic signature compliance, or regulatory documentation review.

alirezarezvani11.7k

Química Computacional

Fda Consultant Specialist

FDA regulatory consultant for medical device companies. Provides 510(k)/PMA/De Novo pathway guidance, QSR (21 CFR 820) compliance, HIPAA assessments, and device cybersecurity. Use when user mentions FDA submission, 510(k), PMA, De Novo, QSR, premarket, predicate device, substantial equivalence, HIPAA medical device, or FDA cybersecurity.

alirezarezvani11.7k

Seguridad

Soc2 Compliance

Use when the user asks to prepare for SOC 2 audits, map Trust Service Criteria, build control matrices, collect audit evidence, perform gap analysis, or assess SOC 2 Type I vs Type II readiness.

alirezarezvani11.7k

Herramientas de Laboratorio

Qms Audit Expert

ISO 13485 internal audit expertise for medical device QMS. Covers audit planning, execution, nonconformity classification, and CAPA verification. Use for internal audit planning, audit execution, finding classification, external audit preparation, or audit program management.

alirezarezvani11.7k

Inmobiliaria y Legal

Quality Manager - QMS ISO 13485 Specialist

ISO 13485 Quality Management System implementation and maintenance for medical device organizations. Provides QMS design, documentation control, internal auditing, CAPA management, and certification support. Use when working with medical device quality systems, preparing for ISO 13485 audits, managing regulatory compliance documentation, setting up corrective actions, or building audit preparation programs. Useful for quality management, audit preparation, regulatory compliance, medical device documentation, and corrective action workflows.

alirezarezvani11.7k

Ventas y Marketing

Head of Regulatory Affairs

Senior Regulatory Affairs Manager for HealthTech and MedTech companies. Prepares FDA 510(k), De Novo, and PMA submission packages; analyzes regulatory pathways for new medical devices; drafts responses to FDA deficiency letters and Notified Body queries; develops CE marking technical documentation under EU MDR 2017/745; coordinates multi-market approval strategies across FDA, EU, Health Canada, PMDA, and NMPA; and maintains regulatory intelligence on evolving standards. Use when users need to plan or execute FDA submissions, navigate 510(k) or PMA approval processes, achieve CE marking, prepare pre-submission meeting materials, write regulatory strategy documents, respond to agency queries, or manage compliance documentation for medical device market access.

alirezarezvani11.7k

Depuración

danielmiessler-personal-ai-infrastructure-releases-v4-0-0-claude-skills-investigation-skill-md

OSINT and people-finding — structured investigations, company intel, due diligence, and ethical people search across public records and social media. USE WHEN OSINT, due diligence, company intel, background check, find person, locate, people search, reconnect, public records, reverse lookup, social media search, verify identity, domain lookup, entity lookup, organization lookup, company lookup, threat intel.

danielmiessler11.6k

Flujos de Trabajo Git

Compliance Tracking

Track compliance requirements and audit readiness. Trigger with "compliance", "audit prep", "SOC 2", "ISO 27001", "GDPR", "regulatory requirement", or when the user needs help tracking, preparing for, or documenting compliance activities.

anthropics11.3k

Base de Conocimientos

Regulatory Fallback Research

Handle tool failures when researching regulatory/government content by using fallback methods and domain knowledge

HKUDS5.4k

Depuración

Jobaudit

Audit your OpenClaw cron job history and estimate how much you've spent on AI agents this week.

openclaw4.2k

Administración de Sistemas

arifOS Sense — Constitutional Governance Kernel

Constitutional governance layer for arifOS. Activates when: (1) a request involves irreversible, high-stakes, or externally consequential actions; (2) Arif invokes 888_HOLD human veto; (3) any action touches identity, values, or constitutional boundaries; (4) the agent must decide what may be claimed, held, or executed. arifOS-sense is the non-negotiable governance kernel — not decorative. Triggers on: "evaluate", "is this safe", "should I proceed", "arifOS", "governance", "veto", "hold", "constitutional", "HOLD", "SEAL", "CAUTION", "VOID", "888".

openclaw4.2k

Gestión de Proyectos

Compliance Readiness

AI Compliance Readiness Assessment — evaluate how prepared an organization is for AI governance regulations (EU AI Act, NIST AI RMF, HHS mandates, state bar AI rules). Scores readiness across 8 dimensions and generates an action plan. Use when assessing AI compliance gaps, preparing for audits, or building a governance roadmap.

openclaw4.2k

Gestión de Proyectos

Capa Officer

CAPA system management for medical device QMS. Covers root cause analysis, corrective action planning, effectiveness verification, and CAPA metrics. Use for CAPA investigations, 5-Why analysis, fishbone diagrams, root cause determination, corrective action tracking, effectiveness verification, or CAPA program optimization.

openclaw4.2k

Depuración

Ai Drama Review

AI短剧内容基因检测。零依赖可用：AI直接分析版权疑似、年龄分级违规、小说魔改程度，输出结构化风险图谱。可选配 Python 环境启用三重相似度算法（n-gram / 编辑距离 / TF-IDF）提升精度。结果仅供内容审核参考，不构成法律意见。

openclaw4.2k

Ventas y Marketing

Head of Regulatory Affairs

Senior Regulatory Affairs Manager for HealthTech and MedTech companies. Prepares FDA 510(k), De Novo, and PMA submission packages; analyzes regulatory pathways for new medical devices; drafts responses to FDA deficiency letters and Notified Body queries; develops CE marking technical documentation under EU MDR 2017/745; coordinates multi-market approval strategies across FDA, EU, Health Canada, PMDA, and NMPA; and maintains regulatory intelligence on evolving standards. Use when users need to plan or execute FDA submissions, navigate 510(k) or PMA approval processes, achieve CE marking, prepare pre-submission meeting materials, write regulatory strategy documents, respond to agency queries, or manage compliance documentation for medical device market access.

openclaw4.2k

Ventas y Marketing

Fda Guideline Search

Search FDA industry guidelines by therapeutic area or topic. Trigger when user requests FDA guidance documents, regulatory guidelines, or asks about FDA requirements for specific disease areas, drug development, or therapeutic categories (e.g., oncology, cardiology, rare diseases). Also triggered by queries about FDA ICH guidelines, FDA guidance documents, or regulatory compliance requirements.

openclaw4.2k

Oficiales de cumplimiento

Oficiales de cumplimiento

Customs Trade Compliance

Customs & Trade Compliance

Quality & Non-Conformance Management

Quality Nonconformance

Gdpr Data Handling

Pci Compliance

Customs Trade Compliance

Fda Food Safety Auditor

Data Privacy Compliance

Compliance

Quality Manager Qmr

Capa Officer

Mdr 745 Specialist

Gdpr Dsgvo Expert

Quality Documentation Manager

Fda Consultant Specialist

Soc2 Compliance

Qms Audit Expert

Quality Manager - QMS ISO 13485 Specialist

Head of Regulatory Affairs

danielmiessler-personal-ai-infrastructure-releases-v4-0-0-claude-skills-investigation-skill-md

Compliance Tracking

Regulatory Fallback Research

Jobaudit

arifOS Sense — Constitutional Governance Kernel

Compliance Readiness

Capa Officer

Ai Drama Review

Head of Regulatory Affairs

Fda Guideline Search