Lead Validation Engineer - Pharma Packaging (6-Month)

Spectraforce Technologies, Inc.; Cincinnati (OH); Presencial; USD 83.000 - 124.000; A tiempo parcial

Descripción de la vacante

Spectraforce Technologies, Inc. is seeking a Validation Engineer in Cincinnati, OH to lead validation, maintenance, and engineering activities within the clinical packaging area.

You will collaborate with operations, engineering services, and external vendors to ensure equipment, facilities, and utilities meet quality standards. The role requires a BS in engineering and 5+ years in validation/engineering in pharma, with experience in validating documents and understanding regulatory

Formación

• BS in engineering and 5+ years in validation/engineering within the pharmaceutical field.
• Experience creating and executing validation documents in VMS.
• Familiarity with Client engineering and financial systems.
• Understanding of Client Engineering Standards and pharmaceutical packaging equipment.

Responsabilidades

• Lead maintenance, engineering, and validation activities in the clinical packaging area.
• Coordinate with operations, engineering services, and third-party vendors.
• Manage validation documentation and Validation Master Plan (VMP).
• Interface with area managers to balance capacity and cost reductions.
• Ensure validation documents are complete and reviewed for quality and compliance.
• Investigate and resolve validation-related issues and drive quality improvement projects.
• Represent department in internal and external quality audits.

Conocimientos

Validation engineering

Pharmaceutical knowledge

Educación

Bachelor's Degree in Engineering

Descripción del empleo

Spectraforce Technologies, Inc. is seeking a Validation Engineer in Cincinnati, OH to lead validation, maintenance, and engineering activities within the clinical packaging area.

You will collaborate with operations, engineering services, and external vendors to ensure equipment, facilities, and utilities meet quality standards. The role requires a BS in engineering and 5+ years in validation/engineering in pharma, with experience in validating documents and understanding regulatory