×
Register Here to Apply for Jobs or Post Jobs. X

Sr. Engineering Project Manager; Medical Devices or Pharma Domain

Job in Sunnyvale, Santa Clara County, California, 94087, USA
Listing for: Maxonic Inc.
Full Time position
Listed on 2026-02-20
Job specializations:
  • Engineering
    Manufacturing Engineer, Quality Engineering
Salary/Wage Range or Industry Benchmark: 100000 USD Yearly USD 100000.00 YEAR
Job Description & How to Apply Below
Position: Sr. Engineering Project Manager (Medical Devices or Pharma Domain)

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.
Required Experience
  • 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.
#J-18808-Ljbffr
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)

Job Posting Language
Employment Category
Education (minimum level)
Filters
Education Level
Experience Level (years)
Posted in last:
Salary