300 件（borghei のリポジトリ） ・ 人気順
概要と使いどころ
NIST Cybersecurity Framework 2.0 implementation, assessment, and compliance management. Use for CSF 2.0 gap analysis, cybersecurity risk management, maturity assessment, CSF profiles, and cross-framework compliance mapping.
日本語の概要は準備中です。原文の説明を表示しています。
PCI DSS v4.0 payment card data security compliance, assessment, and implementation. Use for PCI DSS scoping, cardholder data environment (CDE) security, SAQ and ROC preparation, QSA engagement, tokenization, and merchant compliance.
日本語の概要は準備中です。原文の説明を表示しています。
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.
日本語の概要は準備中です。原文の説明を表示しています。
ISO 13485 Quality Management System implementation and maintenance for medical device organizations. Provides QMS design, documentation control, internal auditing, CAPA management, and certification support.
日本語の概要は準備中です。原文の説明を表示しています。
EU AI Act (Regulation EU 2024/1689) compliance specialist. Use for AI system risk classification, provider/deployer obligations, GPAI model compliance, conformity assessments, bias and fairness testing, and AI governance programs.
日本語の概要は準備中です。原文の説明を表示しています。
Medical device risk management specialist implementing ISO 14971 throughout product lifecycle. Provides risk analysis, risk evaluation, risk control, and post-production information analysis.
日本語の概要は準備中です。原文の説明を表示しています。
Continuous product discovery research operations — picking the method that fits the question, recruiting and screening participants, building interview guides, and scoring evidence into insights. Use when planning or running discovery.
日本語の概要は準備中です。原文の説明を表示しています。
Translate one internal roadmap into audience-appropriate formats with confidence-band discipline. Use when preparing a roadmap readout, tailoring it for an exec, customer, eng, or sales audience, or auditing over-promise risk.
日本語の概要は準備中です。原文の説明を表示しています。
Customer success across onboarding, adoption, retention, and expansion. Use when designing onboarding playbooks, calculating health scores, building QBR decks, planning renewal strategies, or identifying expansion opportunities.
日本語の概要は準備中です。原文の説明を表示しています。
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.
日本語の概要は準備中です。原文の説明を表示しています。
Linear expert for workspace/team admin, Cycles, Projects, Initiatives, Roadmaps, GraphQL API queries, triage workflows, GitHub integration, bulk operations, and Jira-to-Linear migration.
日本語の概要は準備中です。原文の説明を表示しています。
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.
日本語の概要は準備中です。原文の説明を表示しています。
Market sizing and market structure work — TAM/SAM/SOM built top-down and bottom-up then reconciled, segmentation, demand triangulation, and survey design. Use when sizing a market, writing a sizing memo, or fielding a survey.
日本語の概要は準備中です。原文の説明を表示しています。
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.
日本語の概要は準備中です。原文の説明を表示しています。
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.
日本語の概要は準備中です。原文の説明を表示しています。
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.
日本語の概要は準備中です。原文の説明を表示しています。
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.
日本語の概要は準備中です。原文の説明を表示しています。
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.
日本語の概要は準備中です。原文の説明を表示しています。
Administer the Atlassian suite (Jira/Confluence): user provisioning, groups, SSO/SAML, permissions, security policies, marketplace apps, backups, and org-wide governance. Use for admin config, access management, and system optimization.
日本語の概要は準備中です。原文の説明を表示しています。
NIS2 Directive (EU 2022/2555) compliance for critical infrastructure entities, covering the 10 minimum security measures. Use for NIS2 compliance assessments, entity scope analysis, supply chain security, and incident reporting readiness.
日本語の概要は準備中です。原文の説明を表示しています。
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.
日本語の概要は準備中です。原文の説明を表示しています。
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.
日本語の概要は準備中です。原文の説明を表示しています。
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.
日本語の概要は準備中です。原文の説明を表示しています。
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.
日本語の概要は準備中です。原文の説明を表示しています。