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Project Manager

EPS Connects

Rhode Island

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JOB DETAILS
SKILLS
Budget Management, Communication Skills, Contract Manufacturing, Cross-Functional, Customer Relations, Detail Oriented, Documentation, FDA (Food and Drug Administration), ISO (International Organization for Standardization), Lean Manufacturing, Lean Six Sigma, Machining, Manufacturing, Manufacturing Management, Manufacturing/Industrial Processes, Medical Equipment, Medical Products, Microsoft Project, Molding Processes, Organizational Skills, Problem Solving Skills, Process Development, Process Validation, Product Design, Product Support, Product/Service Launch, Project Lifecycle, Project Management Professional (PMP), Project Planning, Project Tracking, Project/Program Management, Regulations, Regulatory Requirements, Requirements Validation/Verification, Risk Analysis, Risk Management, Semiconductor Manufacturing, Time Management, Validation Documentation
LOCATION
Rhode Island
POSTED
23 days ago

Project Manager – Manufacturing (Medical Device / NPI Focus)


Providence, RI | Onsite


We’re partnering with a vertically integrated medical device contract manufacturer supporting product design through full-scale production of finished devices. This environment is fast-paced, customer-driven, and highly regulated—serving leading MedTech, diagnostics, and drug delivery companies.


This role is focused specifically on manufacturing and NPI-driven projects within a regulated environment, where coordination, execution, and attention to detail directly impact product quality and customer success.


What You’ll Be Responsible For


  • Lead new product introduction (NPI) and manufacturing transfer projects from kickoff through production
  • Build and manage detailed project plans using tools such as Microsoft Project, ensuring alignment across timelines, resources, and deliverables
  • Serve as a key point of contact for internal stakeholders and customers throughout the project lifecycle
  • Coordinate cross-functional teams across engineering, quality, and operations to ensure project requirements are met
  • Drive execution around IQ/OQ/PQ, validation activities, and regulatory documentation
  • Monitor project progress and performance, proactively identifying risks and implementing mitigation strategies
  • Ensure projects are delivered on time, within scope, and within budget while meeting quality and regulatory requirements
  • Prepare and maintain project documentation tied to validation, customer requirements, and regulatory standards
  • Facilitate regular project meetings to communicate updates, address challenges, and maintain alignment


What This Role Requires


  • Experience managing projects in a regulated manufacturing environment (medical device strongly preferred)
  • Strong understanding of manufacturing processes (machining, molding, assembly, or similar)
  • Hands-on exposure to NPI, process development, or manufacturing transfer work
  • Ability to work cross-functionally and stay close to the floor—not just manage timelines
  • Comfortable operating in a customer-facing, contract manufacturing environment
  • Strong organizational, communication, and documentation skills


Preferred (But Not Required)


  • PMP certification
  • Experience with ISO 13485 / FDA-regulated environments
  • Background in Lean Manufacturing / Six Sigma or structured problem solving


Why This Role Stands Out


This is a high-impact position inside a growing contract manufacturing environment where project management is directly tied to customer delivery, product quality, and operational performance.

You won’t just be tracking timelines—you’ll be helping bring complex medical products from concept into stable production.


About the Company

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EPS Connects