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.
Numbers & Facts
Location
Blue ash, OH
Skills
Automationunmatched
Castingunmatched
Commissioningunmatched
Communication Skillsunmatched
Corporate Policiesunmatched
Cross-Functionalunmatched
Data Analysisunmatched
Distribution Channelunmatched
FDA (Food and Drug Administration)unmatched
FDA Requirementsunmatched
Geometric Dimensioning and Tolerancingunmatched
Interpersonal Skillsunmatched
Literacyunmatched
Machiningunmatched
Maintain Complianceunmatched
Manufacturingunmatched
Manufacturing Engineeringunmatched
Manufacturing Process Engineeringunmatched
Manufacturing Requirementsunmatched
Manufacturing/Industrial Processesunmatched
Medical Equipmentunmatched
Microsoft Officeunmatched
Minitabunmatched
OEM (Original Equipment Manufacturer)unmatched
Operations Processesunmatched
Persuasion Skillsunmatched
Presentation/Verbal Skillsunmatched
Problem Solving Skillsunmatched
Process Validationunmatched
Product Lifecycle Managementunmatched
Regulatory Requirementsunmatched
Requirements Managementunmatched
Root Cause Analysisunmatched
Statisticsunmatched
Technical Writingunmatched
Validation Documentationunmatched
Validation Planunmatched
Writing Skillsunmatched
🎯
Be found by employers
5,500+ employers search our resume database daily. Add yours to get found by recruiters looking for candidates like you.
Level up your application
Professional resume templates
Browse dozens of recruiter approved resume templates, layouts and formats. Choose your favorite and make it your own in minutes.