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Manufacturing Engineer

  • Manufacturing Engineer job type Posted on: Oct 28, 2026
  • Manufacturing Engineer experience level Katalyst Healthcares & Life Sciences
  • Manufacturing Engineer employment type Morgantown, Kentucky
  • Manufacturing Engineer employment type Onsite
  • Manufacturing Engineer salary Full-time

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Job Title :

Manufacturing Engineer

Job Type :

Full-Time

Job Location :

Morgantown Kentucky United States

Remote :

No

Jobcon Logo Job Description :

Job Description

Job Description
Roles & Responsibilities:
  • Support in Manufacturing process remediation and readiness activities for new product launch.
  • Support Design Transfer deliverables, including tracking and scheduling.
  • Support/Initiate Change Order for manufacturing documentation such as but not limited to, manufacturing procedures, shop floor paperwork, and inspection procedures.
  • Risk Management updates PFMEA.
  • Part creation in Windchill. BOM and configuration management.
  • Work with cross functional teams as required, especially with R&D, Quality, and Regulatory teams.
  • Complies with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments. Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors.
Requirements:
  • Knowledge of ISO and/or FDA quality system regulations as it pertains to design transfer and process control.
  • Previous medical device experience
  • 5 years of Medical device Manufacturing experience

Jobcon Logo Position Details

Posted:

Oct 28, 2026

Reference Number:

79f53aca

Employment:

Full-time

City:

Morgantown

Job Origin:

ziprecruiter

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Job Description

Job Description
Roles & Responsibilities:
  • Support in Manufacturing process remediation and readiness activities for new product launch.
  • Support Design Transfer deliverables, including tracking and scheduling.
  • Support/Initiate Change Order for manufacturing documentation such as but not limited to, manufacturing procedures, shop floor paperwork, and inspection procedures.
  • Risk Management updates PFMEA.
  • Part creation in Windchill. BOM and configuration management.
  • Work with cross functional teams as required, especially with R&D, Quality, and Regulatory teams.
  • Complies with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments. Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors.
Requirements:
  • Knowledge of ISO and/or FDA quality system regulations as it pertains to design transfer and process control.
  • Previous medical device experience
  • 5 years of Medical device Manufacturing experience

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