Description

You will manage commissioning and qualification activities within a cGMP manufacturing environment.

Responsibilities

• Execute equipment commissioning protocols for specialized pharmaceutical manufacturing tools.
• Perform qualification activities to ensure compliance with cGMP standards.
• Validate technical systems and equipment within the manufacturing facility.
• Document all validation and commissioning processes according to regulatory requirements.

Required Skills

• 3+ years of experience in commissioning or validation roles.
• Hands-on experience with equipment commissioning.
• Technical knowledge of freezers and isolators.
• Direct experience working within cGMP manufacturing environments.
• Degree in any field.

Key Skills

Education

ANY GRADUATE