Quality Validation Expert (IQ/OQ/PQ)

Natural Essentials; Aurora (OH); On-site; USD 70,000 - 90,000; Full time

Job summary

A pharmaceutical company located in Aurora, Ohio is seeking a Quality Validation Specialist to perform critical validation and qualification activities in a cGMP environment. The position requires at least four years of GMP experience and a Bachelor's in Engineering. Responsibilities include writing validation protocols, analyzing quality data, and troubleshooting complex issues. Strong organizational skills and the ability to manage multiple tasks are essential. Full-time role with compensation based on experience.

Qualifications

• Minimum of four (4) years of relevant GMP metrology, validation, or process engineering experience.
• Previous FDA experience is a plus.
• Ability to work independently or as a team member.

Responsibilities

• Write and execute validation and re-validation protocols and reports.
• Analyze statistical data to verify acceptable criteria.
• Troubleshoot and rectify complex issues.

Skills

Strong organization and communication skills

Ability to manage multiple priorities

Detail oriented

Experience with Google Suite

Strong written and verbal communication

Education

Bachelor’s Degree in Engineering or a related degree

Tools

Microsoft Office applications

Job description

A pharmaceutical company located in Aurora, Ohio is seeking a Quality Validation Specialist to perform critical validation and qualification activities in a cGMP environment. The position requires at least four years of GMP experience and a Bachelor's in Engineering. Responsibilities include writing validation protocols, analyzing quality data, and troubleshooting complex issues. Strong organizational skills and the ability to manage multiple tasks are essential. Full-time role with compensation based on experience.