Description

You will execute engineering validation protocols within a pharmaceutical manufacturing environment.

This role is on-site.

Responsibilities

• Execute equipment qualification protocols to ensure compliance with engineering standards.
• Develop and implement sampling plans for validation activities.
• Perform cleaning validation to verify process efficacy.
• Conduct root cause analysis to resolve validation deviations.
• Manage the formal approval process for validation documentation.

Required Skills

• 5+ years of experience in validation or engineering roles.
• Hands-on experience with equipment qualification.
• Proficiency in cleaning validation methodologies.
• Experience designing and executing sampling plans.
• Ability to perform technical root cause analysis.
• Knowledge of formal approval processes for engineering documentation.
• Bachelor's degree or equivalent graduate-level education.

Key Skills

Education

ANY GRADUATE