pm-skills
6 production-ready project management skills for Atlassian users: senior PM with portfolio management, scrum master with velocity forecasting, Jira expert with JQL mastery, Confluence expert, Atlassian admin, and template creator. MCP integration for live Jira/Confluence automation. Works with Claude Code, Codex CLI, and OpenClaw.
- License 许可
- MIT
- 最近更新
- 2026-03-13
- Stars
- ★ 4
- Forks
- 0
01 前言 Front Matter
- name
- pm-skills
- tags
- [ "project-management", "jira", "confluence", "atlassian", "scrum", "agile" ]
- agents
- [ "claude-code", "codex-cli", "openclaw" ]
- author
- Alireza Rezvani
- license
- MIT
- version
- 1.0.0
- description
- 6 production-ready project management skills for Atlassian users: senior PM with portfolio management, scrum master with velocity forecasting, Jira expert with JQL mastery, Confluence expert, Atlassian admin, and template creator. MCP integration for live Jira/Confluence automation. Works with Claude Code, Codex CLI, and OpenClaw.
02 资源文件 7
- 参考文档.claude-plugin/plugin.json501 B
- 参考文档.codex/instructions.md966 B
- 参考文档CLAUDE.md5.4 KB
- 参考文档IMPLEMENTATION_SUMMARY.md8.7 KB
- 参考文档INSTALLATION_GUIDE.txt2.6 KB
- 参考文档README.md13.9 KB
- 参考文档REAL_WORLD_SCENARIO.md17.2 KB
03 SKILL.md 正文
Project Management Skills
6 production-ready project management skills with Atlassian MCP integration.
Quick Start
Claude Code
/read project-management/jira-expert/SKILL.md
Codex CLI
npx agent-skills-cli add alirezarezvani/claude-skills/project-management
Skills Overview
| Skill | Folder | Focus |
|---|---|---|
| Senior PM | senior-pm/ |
Portfolio management, risk analysis, resource planning |
| Scrum Master | scrum-master/ |
Velocity forecasting, sprint health, retrospectives |
| Jira Expert | jira-expert/ |
JQL queries, workflows, automation, dashboards |
| Confluence Expert | confluence-expert/ |
Knowledge bases, page layouts, macros |
| Atlassian Admin | atlassian-admin/ |
User management, permissions, integrations |
| Atlassian Templates | atlassian-templates/ |
Blueprints, custom layouts, reusable content |
Python Tools
6 scripts, all stdlib-only:
python3 senior-pm/scripts/project_health_dashboard.py --help
python3 scrum-master/scripts/velocity_analyzer.py --help
Rules
- Load only the specific skill SKILL.md you need
- Use MCP tools for live Jira/Confluence operations when available
04 同仓库更多 Skills
risk-management-specialist
Medical device risk management specialist implementing ISO 14971 throughout product lifecycle. Provides risk analysis, risk evaluation, risk control, and post-production information analysis. Use when user mentions risk management, ISO 14971, risk analysis, FMEA, fault tree analysis, hazard identification, risk control, risk matrix, benefit-risk analysis, residual risk, risk acceptability, or post-market risk.
regulatory-affairs-head
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.
quality-manager-qms-iso13485
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.
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.
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.
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.