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How much do ecn jobs pay per hour?

As of Aug 17, 2026, the average hourly pay for ecn in the United States is $25.64, according to ZipRecruiter salary data. Most workers in this role earn between $18.99 and $31.25 per hour, depending on experience, location, and employer.

What is an ECN?

An ECN (Engineering Change Notice) job involves managing and documenting modifications to product designs, manufacturing processes, or engineering specifications. Professionals in this role ensure that changes are properly reviewed, approved, and implemented to maintain product quality and compliance. They typically collaborate with engineers, product managers, and manufacturing teams to track revisions and maintain accurate records.

What are the key skills and qualifications needed to thrive in the ECN position?

To excel as an ECN (Engineered Change Notice) Coordinator, strong organizational skills, technical understanding of manufacturing or engineering processes, and attention to detail are essential, typically backed by relevant experience or a technical degree. Familiarity with product lifecycle management (PLM) systems, document control software, and knowledge of industry standards or certifications is highly beneficial. Effective communication, collaboration, and time management are crucial soft skills for coordinating between engineering, production, and quality teams. These abilities ensure timely and accurate implementation of engineering changes, minimizing production disruptions and maintaining product quality.

What are some of the main challenges faced by ECN coordinators, and how are they addressed?

ECN Coordinators often face the challenge of balancing multiple change requests and ensuring all involved departments stay informed and aligned throughout the process. Coordinating approvals, tracking documentation, and managing deadlines can require strong organizational skills and proactive communication. Many companies support ECN Coordinators with dedicated PLM tools and clearly defined workflows to streamline updates and track progress efficiently. Working closely with cross-functional teams helps address potential bottlenecks quickly. As you gain experience in the role, you'll develop strategies and relationships that make handling these complexities much more manageable.

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Ecn jobs near you
Infographic showing various Ecn job openings in the United States as of August 2026, with employment types broken down into 75% Full Time, and 25% Contract. Highlights an 100% In-person job distribution, with an average salary of $53,329 per year, or $25.6 per hour.

Medical Device Component Development Engineer

PB consulting

Morrow, OH • On-site

Full-time

This job post has expired today. Applications are no longer accepted.

Job description

We are seeking a Medical Device Component Development Engineer to support component development, product lifecycle management, and engineering change activities for regulated medical devices. The ideal candidate will have expertise in design controls, verification & validation, supplier quality, process validation, and regulatory compliance.

Roles and Responsibilities
  • Lead component development and engineering change projects from concept to implementation.
  • Manage project timelines, risks, and cross-functional coordination.
  • Support Design Verification & Validation (V&V), test protocols, and technical documentation.
  • Partner with suppliers on component qualification, DFM reviews, tooling, and process capability.
  • Support manufacturing transfer, IQ/OQ/PQ, pilot builds, and production readiness.
  • Apply Design Controls, PLM, ECO/ECN/ECR, Risk Management, and Quality System requirements.
  • Review engineering drawings, GD&T, specifications, and acceptance criteria.
  • Drive root cause analysis using CAPA, 8D, 5 Whys, and Fishbone methodologies.
  • Communicate project status, risks, and technical recommendations to stakeholders.
Required Qualifications
  • Experience in Medical Device Component Development or Product Development.
  • Strong knowledge of:
    • Product Lifecycle Management (PLM)
    • Design Controls & Engineering Change Management (ECO/ECN/ECR)
    • Design Verification & Validation (V&V)
    • ISO 14971, DFMEA, PFMEA
    • ISO 13485 & FDA 21 CFR Part 820/QMSR
    • Supplier Quality Engineering & Design for Manufacturability (DFM)
    • Process Validation (IQ/OQ/PQ)
    • GD&T and engineering drawings
  • Strong project management, communication, and problem-solving skills.
  • Experience working with cross-functional teams in a regulated medical device environment.
Preferred Skills
  • Medical Device Product Development
  • Supplier Quality & Component Qualification
  • Risk Management & Regulatory Compliance
  • Manufacturing Transfer & Validation
  • Root Cause Analysis (CAPA, 8D)
  • Stakeholder & Project Management

Apply