CQV Engineer II

Description

• Delivers scope of work within budgeted hours
• Applying the principals of good documentation practices (CGDP)
• Collaborate in a multi discipline team environment
• Document development as well as testing execution to meet client qualification needs
• Independently perform qualification protocols and review other team members qualification documents
• Ensure the implementation of current good manufacturing practices (CGMP)
• Performs work in compliance with PM Group’s Service Delivery Platforms and Quality Management System (QMS)

Requirements

• 2 + Years of CQV experience in the Pharmaceutical, Biotech, Life Science and/or Cell & Gene Therapy industries
• Demonstrates an understanding of project scope of work assigned
• Bachelor’s degree is required; an engineering degree is preferred
• Experience working with current good engineering and current good manufacturing practices
• Demonstrated experience working in an industry regulated life sciences environment
• Understanding of the entire validation life cycle and change control process
• The ability to travel as needed for client development and project execution
• Good technical reporting writing skills are mandatory
• Knowledge of cGMP Manufacturing environments is preferred

Benefits

Training + Development

Interview process

Visa Sponsorship

Security clearance