Project Manager - MES (Medical Devices / Life Sciences)

Remote • Posted 4 days ago • Updated 4 days ago
Contract Corp To Corp
Contract Independent
Contract W2
6 Months
No Travel Required
Remote
Depends on Experience
Fitment

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Job Details

Skills

  • Project Manager
  • MES

Summary

Title: Project Manager - MES (Medical Devices / Life Sciences)
Location: Pittsburgh, PA (Remote)
Experience: 10+ years
 
About the Role
We are seeking an experienced Project Manager (PM) to lead the implementation and delivery of Manufacturing Execution Systems (MES) within a highly regulated medical devices/life sciences environment. This role requires strong technical expertise, regulatory knowledge, and leadership capabilities to manage cross-functional teams and ensure compliance with FDA and industry standards.
 
Key Responsibilities
 
Project Planning & Execution
  •  
  • Define project scope, objectives, and deliverables in collaboration with senior management and key stakeholders.Develop comprehensive project plans including timelines, milestones, and resource allocation.Drive end-to-end execution of MES implementation projects, ensuring alignment with organizational goals.
  • Budget & Resource Management
  • Forecast project requirements and manage budgets effectively.Track project expenses and identify/mitigate variances proactively.Optimize resource utilization across teams and project phases.
Team Leadership & Delivery
  • Lead cross-functional teams including software engineers, automation specialists, and QA teams.Delegate tasks effectively, ensuring accountability and high performance.Drive delivery using Agile or hybrid SDLC methodologies.
  • Risk Management & Compliance
  • Identify and mitigate project risks, issues, and bottlenecks.Ensure adherence to cybersecurity, data integrity, and validation requirements.Maintain audit trails and ensure compliance with Device History Records (DHR) requirements.
Stakeholder Communication
  • Act as the primary point of contact for stakeholders.Provide regular status updates, performance metrics, and executive reports.Facilitate communication between business, IT, and manufacturing teams.
Quality Assurance & Project Closeout
  • Ensure project deliverables meet quality, regulatory, and organizational standards.Oversee post-implementation validation and documentation.Conduct post-project reviews to identify continuous improvement opportunities.
Compliance & Validation
  • Lead Computer System Validation (CSV) processes ensuring all MES applications meet regulatory standards.Ensure compliance with FDA 21 CFR Part 11 and GAMP guidelines.Manage validation documentation including IQ/OQ/PQ protocols.

Shop Floor Integration
  • Oversee integration of .NET-based MES systems with plant floor systems (PLCs, SCADA).Enable connectivity between manufacturing operations and enterprise systems (ERP).Ensure traceability for production metrics and genealogy tracking.

eDHR Implementation
  • Lead transition from paper-based systems to Electronic Device History Records (eDHR).Collaborate closely with IT, Quality, and Manufacturing teams to ensure seamless adoption.
Required Qualifications
Technical Expertise
  • 10+ years of strong proficiency in:
•    C#, ASP.NET, .NET CoreSQL ServerWPF or Blazor (for HMI/Dashboard development)
•    5+ years of experience with MES architecture and shop floor system integration (PLCs, SCADA).
 
Domain Experience
•    Proven experience managing MES implementations in:
•    Life SciencesMedical Devices (Class II/III preferred)
 
Certifications
  • PMP (Project Management Professional) OR Certified Scrum Master (CSM)Strong understanding of Quality Management Systems (QMS)
  • Regulatory Knowledge
  • Familiarity with:
    • FDA 21 CFR Part 11GAMP standardsISO 13485FDA Design Controls
Validation Expertise
  • Hands-on experience with Computer System Validation (CSV)Strong documentation and audit readiness experience
 
Key Skills
  • Strong leadership and stakeholder managementExcellent communication and reporting skillsRisk assessment and mitigation expertiseAnalytical and problem-solving mindsetAbility to manage complex, regulated projects
 
Preferred Qualifications
  • Experience with eDHR implementationsExposure to digital transformation initiatives in manufacturingKnowledge of cybersecurity frameworks in regulated environments
  • Initiatives in manufacturingKnowledge of cybersecurity frameworks in regulated environments
 
Regards
Krishna
 

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Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
  • Dice Id: 10204540
  • Position Id: 85396-2308-92990
  • Posted 4 days ago
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