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Manufacturing Process Engineer

Job in Raynham, Bristol County, Massachusetts, 02767, USA
Listing for: Kaztronix LLC
Full Time position
Listed on 2026-01-13
Job specializations:
  • Engineering
    Manufacturing Engineer, Quality Engineering, Process Engineer
  • Manufacturing / Production
    Manufacturing Engineer, Quality Engineering
Job Description & How to Apply Below

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, OpEx, 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.
Qualifications Education
  • Bachelor of Science Degree from accredited institution in Manufacturing Engineering, Mechanical Engineering, Industrial Engineering, or a related degree.
Experience and Skills Required
  • 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.
Preferred
  • 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.
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