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Zusammenfassung
A leading engineering company in El Paso is looking for a qualified individual to coordinate manufacturing processes for custom equipment and tooling. Responsibilities include supporting suppliers, executing protocols, and ensuring compliance with quality standards. Candidates must possess a Bachelor's Degree in Engineering and have over 5 years of experience in manufacturing, new product transfers, and product/process development.
Qualifikationen
5+ years of experience in Manufacturing.
5+ years of experience in New Product Transfers.
5+ years of experience in Product / Process Development.
Aufgaben
Coordinates and Supports Suppliers for Manufacturing of Custom Equipment/Tooling.
Coordinates purchase and delivery of Equipment/Tooling.
Coordinates installation of Equipment/Tooling.
Develops and Executes IQ and OQ Protocols and Reports.
Develops and Executes Test Method Validations / Gage R&R.
Generates and Issues for Approval SOPs and Manufacturing Procedures.
Develops and Executes Component Qualifications.
Develops and Executes PQ and PPQ Protocols and Reports.
Develops Manufacturing Capacity Analysis.
Develops and Executes Process Characterizations / Design of Experiments (DOE).
Develops documentation/justification for assigned capital projects.
Complies with cGMP's, Quality Standards, and established policies.
Executes other duties assigned by his supervisor.
Ausbildung
Bachelor's Degree in Engineering
Jobbeschreibung
Job Description
• Coordinates and Supports Suppliers for Manufacturing of Custom Equipment/Tooling
• Coordinates purchase and delivery of Equipment/Tooling
• Coordinates installation of Equipment/Tooling
• Develops and Executes IQ and OQ Protocols and Reports
• Develops and Executes Test Method Validations / Gage R&R
• Generates and Issues for Approval SOPs and Manufacturing Procedures
• Develops and Executes Component Qualifications
• Develops and Executes PQ and PPQ Protocols and Reports
• Develops Manufacturing Capacity Analysis
• Develops and Executes Process Characterizations / Design of Experiments (DOE)
• Develops documentation/justification for assigned capital projects
• Complies with cGMP's, Quality Standards , and established policies and
• Executes other duties assigned by his supervisor
Education and/or Experience
• Bachelor's Degree in Engineering
• Experience in the Medical Device / Pharmaceutical Industries: Yes
5+ years of experience in the following fields
• Manufacturing
• New Product Transfers
• Product / Process Development
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