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Sr. Engineering Project Manager; Medical Devices or Pharma Domain
Job in
Sunnyvale, Santa Clara County, California, 94087, USA
Listed on 2026-02-20
Listing for:
Maxonic Inc.
Full Time
position Listed on 2026-02-20
Job specializations:
-
Engineering
Manufacturing Engineer, Quality Engineering
Job Description & How to Apply Below
We are seeking a seasoned Project Manager to lead and execute cross-functional Manufacturing and Process Engineering projects ranging from $100K to $1M+, with experience particularly in a medical device, pharma, or life sciences environment.
This role involves driving project planning, tracking, and execution across Engineering, Operations, Regulatory, and Supply Chain, while ensuring schedule accuracy, resource forecasting and leverage, and risk management.
Responsibilities- Lead and manage Engineering projects from planning through execution.
- Develop detailed project schedules and track project health, risks, resource utilization at the process engineering organization level and milestones.
- Forecast, load, and track resource allocations in Clarity PPM or Smartsheet; track budgets and actuals using Excel or Anaplan.
- Facilitate weekly/biweekly cross-functional prioritization and status meetings and drive accountability for all $100K+ process engineering projects.
- Identify opportunities for resource utilization and enable efficiencies, cost optimization, project risk management, and define and track success metrics.
- Collaborate with stakeholders across Design, Manufacturing, Global Ops (Manufacturing and Supply Chain), and Product Quality.
- 15+ years of project management experience in Manufacturing/Process Engineering projects.
- Manufacturing Product development knowledge is a must.
- Strong experience with Clarity PPM, Smartsheet, MS Project, budget tracking tools.
- Awareness of Goal tracking tools like is nice to have.
- Proven ability to manage cross-functional stakeholders, risks, and mitigation plans.
- PMP or Agile Methodologies certification and background in medical devices or regulated industries are required.
- Exceptional communication and organizational skills with the ability to work independently or collaboratively; demonstrates strategic thinking, executes tactically with urgency, prioritizes effectively, and proactively identifies and mitigates risks with teams.
- Has experience working efficiently with VPs, directors and engineers.
- Experience in a medical device, pharma, or life sciences environment.
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