Path Engineering

As a Principal Validation Specialist (also known as Quality Assurance Specialist, Validation Engineer), you'll manage all phases of complex validation project activities, ensuring regulatory compliance. You'll be responsible for assuring compliance of validated systems, processes, and equipment to current cGMP, FDA, EU, USDA requirements. Your duties will also include project management for validation activities, contractor oversight, document review, deviation management, and CAPA assessment.

• Competitive compensation and benefits program.
• Opportunities for international collaboration and direct contribution to company success.
• Support for employee development, fostering a healthy working environment, meaningful work, diversity and inclusion, mobility, networking, and work-life balance.

• Bachelor's Degree in a relevant scientific, bioengineering or relevant discipline.
• Minimum of six (6) years GMP validation or similar experience in a GMP manufacturing or similar production environment.
• Excellent written and verbal communication skills and proficiency in office application software (MS-Word, MS-Excel, MS-Outlook, PowerPoint).