Validation Engineer

Raritan, NJ, US • Posted 30+ days ago • Updated 6 hours ago

Full Time

On-site

Fitment

Dice Job Match Score™

⭐ Evaluating experience...

Job Details

Skills

Writing
IQ
OQ
PQ
Root Cause Analysis
Conflict Resolution
Problem Solving
Reporting
Presentations
Billing
Plant Lifecycle Management
Product Lifecycle Management
Regulatory Compliance
Collaboration
Science
Manufacturing Engineering
Mechanical Engineering
Industrial Engineering
Process Engineering
Technical Writing
Management
Manufacturing
Communication
Microsoft Office
Medical Devices
Machining
Data Analysis
Minitab
GD&T

Summary

Summary:
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.
Roles & Responsibilities:

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.

Education & Experience:

Bachelor of Science Degree from accredited institution in Manufacturing Engineering, Mechanical Engineering, Industrial Engineering, or a related degree.
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.

Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.

Dice Id: 91116760
Position Id: 15b761ed462358aacf426d9503172548
Posted 30+ days ago

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