Global Project Manager (m/f/d)

P.I. Works Inc

Basel

Vor Ort

CHF 120.000 - 170.000

Vollzeit

14 Tage+
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Zusammenfassung

P.I. Works Inc in Basel, Switzerland seeks an experienced Project Manager to lead cross-functional development programs in medical devices and combination products.

You will own scope, timelines, risks, and budgets, apply best-practice project management tools, ensure design control compliance (21 CFR 820), foster collaboration, and communicate transparently with global stakeholders in a fast-paced, international environment.

Qualifikationen

  • Bachelor's degree in Engineering or related field required.
  • Experience in project management in global medical device, pharmaceutical, or biopharmaceutical settings.
  • Experience with drug and/or medical device development and combination products.
  • Knowledge of PM best practices and tools; PMP certification is a plus.
  • Familiarity with 21 CFR 820.30 design control requirements.
  • Experience collaborating with vendors/partners.
  • Excellent communication and relationship-building skills.
  • Ability to manage complex projects independently in a fast-paced, team-based environment.
  • Fluent English; German, Japanese or Danish is advantageous.

Aufgaben

  • End-to-end project management across development phases aligned with the Device Team plan.
  • Apply best-in-class PM methodologies and tools for planning, risk, and budget tracking.
  • Develop and maintain project plans, including contingency planning.
  • Ensure transparent communication across stakeholders and timely escalation of critical issues.
  • Manage project scope, timelines, and deliverables with cross-functional alignment.
  • Identify, assess, and mitigate risks and issues with corrective actions.
  • Foster a high-performing, collaborative team environment with cross-functional engagement.
  • Build and maintain relationships with internal and external stakeholders.
  • Plan and facilitate meetings, forecast resources, monitor budget, and control costs.
  • Maintain governance, knowledge management, and continuous process improvement.

Kenntnisse

Project management
Stakeholder communication
Risk management
Vendor collaboration
Cross-functional collaboration
English fluency

Ausbildung

Bachelor's degree in Engineering or related field

Tools

Microsoft Project
Smartsheet
Google Suite

Jobbeschreibung

Responsibilities
  • End-to-end responsibility for project management across all development phases (Core, Lifecycle, Technical Development), aligned with the overall Device Team plan.
  • Application of best-in-class project management methodologies and tools for planning, communication, risk/issue management, collaboration, and budget tracking.
  • Development, maintenance, and optimization of project plans (e.g., Design & Development Plan), including contingency planning.
  • Ensuring transparent, structured communication across stakeholders and timely escalation of critical issues.
  • Management of project scope, timelines, and deliverables, ensuring alignment with cross-functional teams and dependencies.
  • Proactive identification, assessment, and mitigation of risks and issues, including implementation of corrective actions.
  • Fostering a high-performing, collaborative team environment through active team-building and cross-functional engagement.
  • Building and maintaining strong relationships with internal and external stakeholders, ensuring effective collaboration.
  • Planning and facilitation of efficient meetings, along with responsibility for resource forecasting, budget monitoring, and cost control.
  • Ensuring governance compliance, structured knowledge management, and continuous improvement of processes, tools, and best practices based on lessons learned.
  • Fascinating, innovative environment in an international atmosphere.
Requirements
  • Bachelor's degree in Engineering or a related field.
  • Experience, with at least a few in a relevant industry, preferably within a global medical device, pharmaceutical, or biopharmaceutical company.
  • Experience in project management in drug and/or medical device development and commercialization, particularly with combination products.
  • Proficiency in Project Management best practices and software (Microsoft Project, Smartsheet, Google suite) - PMP certification is an asset.
  • Knowledge of 21CFR820.30 design control requirements.
  • Experience with vendor / partner collaboration.
  • Excellent communication and relationship-building skills.
  • Ability to manage complex projects independently in a fast-paced, team-based environment.
  • Fluent English is required. German, Japanese or Danish is of advantage.
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