GDPR and German DSGVO compliance. Use for GDPR compliance assessments, privacy audits, scanning codebases for privacy risks, DPIA generation, data protection planning, and data subject rights management.
한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.
300건(borghei의 저장소) · 인기순
GDPR and German DSGVO compliance. Use for GDPR compliance assessments, privacy audits, scanning codebases for privacy risks, DPIA generation, data protection planning, and data subject rights management.
한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.
Sales execution across pipeline, discovery, demos, negotiation, and closing. Use when qualifying opportunities, running MEDDIC discovery, building account plans, handling objections, structuring proposals, or forecasting pipeline.
한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.
Document control for medical device QMS, covering numbering, version control, change management, and 21 CFR Part 11 compliance. Use for document control procedures, change control workflows, and electronic signature compliance.
한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.
Confluence expert for spaces, knowledge bases, documentation, page layouts, macros, templates, and Jira-Confluence integration. Use for documentation strategy, space architecture, content organization, and collaborative knowledge management.
한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.
Structured intelligence dossiers on companies, people, markets, or domains, with source triangulation and fact/inference discipline. Use when preparing a deal-prep dossier, executive briefing, or due-diligence overview.
한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.
Notion expert for product management workflows. Use for database design for PRDs/OKRs/Roadmaps/Decisions, property and view design, page architecture, Notion REST API, and sync with Jira, Linear, and GitHub.
한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.
CCPA and CPRA California privacy compliance. Use for CCPA/CPRA readiness assessments, personal information data mapping, consumer rights handling, privacy policy review, opt-out mechanisms, and California privacy audits.
한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.
FDA regulatory consultant for medical device companies, covering 510(k)/PMA/De Novo pathways, QSR (21 CFR 820), HIPAA, and device cybersecurity. Use for FDA submissions, predicate and substantial-equivalence analysis, and premarket strategy.
한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.
Senior Regulatory Affairs Manager for HealthTech and MedTech. Use for regulatory strategy, FDA 510(k)/PMA/De Novo submissions, EU MDR CE marking, global market access, and regulatory intelligence.
한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.
Expert delivery management for release planning, deployment strategy, incident response, change management, SLA/error-budget tracking, and DORA metrics across continuous delivery pipelines.
한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.
Create, modify, and govern reusable Jira and Confluence templates, blueprints, and standardized content structures. Use for org-wide templates, custom blueprints, page layouts, and automated content generation.
한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.
Senior PM for enterprise software and SaaS — portfolio management, quantitative risk analysis, prioritization, and executive reporting. Use for portfolio health reviews, board-ready status reports, and multi-project risk/capacity analysis.
한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.
Turn meeting notes into an accountable register — extract decisions, actions and open questions, flag ownerless items, track follow-through. Use when commitments get dropped or a recurring meeting decides nothing.
한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.
UI design system toolkit covering design tokens, component documentation, responsive calculations, and developer handoff. Use for creating design systems, maintaining visual consistency, or facilitating design-dev handoff.
한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.
Data-driven sprint retrospectives from git history — velocity, cycle/lead time, contributor insights, and churn hotspots. Use to run a retrospective, analyze team velocity or throughput, or generate a retro report from commit history.
한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.
CAPA system management for medical device QMS, covering root cause analysis, corrective action planning, and effectiveness verification. Use for CAPA investigations, 5-Why and fishbone analysis, and corrective action tracking.
한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.
Productboard expert for workspace setup, Insight-to-Feature triage, Driver scoring, Releases, Roadmap views, and REST API automation. Use for Productboard administration, prioritization workflows, and programmatic API operations.
한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.
DORA (EU 2022/2554) digital operational resilience compliance for financial entities, covering all 5 pillars. Use for DORA readiness assessments, ICT risk management, incident classification, and third-party ICT oversight.
한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.
Data-driven Scrum Master for sprint health scoring, Monte Carlo velocity forecasting, retrospective analysis, capacity planning, and Tuckman team coaching. Use when facilitating sprint planning, diagnosing velocity, or running retrospectives.
한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.
ISO 13485 Quality Management System implementation and maintenance for medical device organizations. Provides QMS design, documentation control, internal auditing, CAPA management, and certification support.
한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.
Clinical study operations — protocol structure, endpoint selection, eligibility design, sample-size and power planning, site feasibility, and documentation readiness. Use when planning, auditing, or costing a study.
한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.
Grant writing and proposal architecture: funder fit, proposal structure, budget design, and success-factor scoring. Use when writing a grant proposal, evaluating funder fit, auditing a draft for competitiveness, or planning a budget.
한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.
Expert agile coaching: framework selection, maturity assessment, retrospective facilitation, transformation roadmaps. Use when selecting an agile framework, coaching teams, facilitating retrospectives, or designing a transformation.
한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.
ISO 42001 AI Management System (AIMS) compliance. Use for ISO 42001 readiness assessments, AI governance planning, AI impact assessments, Annex A control validation, responsible AI implementation, and AIMS certification preparation.
한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.