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manufacturing Engineer

Karwell Technologies

Blue ash, OH

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JOB DETAILS
SKILLS
Automation, Casting, Commissioning, Communication Skills, Corporate Policies, Cross-Functional, Data Analysis, Distribution Channel, FDA (Food and Drug Administration), FDA Requirements, Geometric Dimensioning and Tolerancing, Interpersonal Skills, Literacy, Machining, Maintain Compliance, Manufacturing, Manufacturing Engineering, Manufacturing Process Engineering, Manufacturing Requirements, Manufacturing/Industrial Processes, Medical Equipment, Microsoft Office, Minitab, OEM (Original Equipment Manufacturer), Operations Processes, Persuasion Skills, Presentation/Verbal Skills, Problem Solving Skills, Process Validation, Product Lifecycle Management, Regulatory Requirements, Requirements Management, Root Cause Analysis, Statistics, Technical Writing, Validation Documentation, Validation Plan, Writing Skills
LOCATION
Blue ash, OH
POSTED
9 days ago

Roles & Responsibilities:

  • Writing and execution of validation protocols and reports (i.e. IQ, OQ, PQ, etc.).
  • Developing and implementing manufacturing processes, preparation of specifications and operator instructions, process studies, production readiness, investigations, root cause analysis, problem solving and report or presentation preparation.
  • Updating procedures, manufacturing specifications, bills, routes and travelers for product & process changes in the PLM system.
  • Working with OEM equipment manufacturers and distributors to develop user requirements.
  • Work on new asset commissioning Working with multi-functional teams (Operations Value Stream, Op Ex, Planning, Engineering, and Quality) to align on validation strategy, author validation documents, coordinate execution and document approvals.
  • Ensuring compliance with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments when supporting projects.
  • Maintains positive and cooperative communication and collaboration with all levels of employees, customers, contractors, and vendors.

Requirements:

  • 2-4 years of experience in manufacturing and/or process engineering.
  • Strong technical writing skills, with appropriate awareness of intended audience.
  • Ability to effectively communicate across multiple audiences, including operators, peers and management, in both written and oral manners Process validation experience.
  • Experience in a Medical Device and/or regulated manufacturing work environment.
  • Persuasive communication and interpersonal skills.
  • Digital literacy, including use of Microsoft Office tools.
  • Experience working in a regulated industry, such as Medical Device.
  • Experience with machining processes, metal finishing processes, laser processing or production automation.
  • Hands-on experience with machining processes, casting, metal finishing processes, laser processing or production automation.
  • Knowledge of statistical data analysis and associated tools (e.g. Minitab).
  • Basic knowledge of Geometric Dimensioning and Tolerancing (GD&T).
  • Willingness to support global projects, which may include travel.

About the Company

K

Karwell Technologies

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