Position Summary:
We are seeking an experienced CQV Lead to oversee the commissioning, qualification, and validation activities for packaging & inspection systems and related projects. The ideal candidate will manage all aspects of CQV execution while ensuring compliance with GMP requirements and industry standards.

Key Responsibilities:
• Lead and coordinate CQV activities for inspection equipment and systems
• Develop and review commissioning, qualification, and validation documentation
• Manage risk assessments and validation master plans
• Oversee equipment qualification activities (IQ/OQ/PQ)
• Interface with vendors, stakeholders, and quality teams
• Review and approve validation protocols and reports
• Ensure compliance with regulatory requirements and company standards
• Mentor and guide CQV team members

Requirements:
• Bachelor's degree in Engineering, Science, or related field
• 7+ years of CQV experience in pharmaceutical/medical device industry
• Strong knowledge of GMP requirements and FDA regulations
• Experience with inspection systems and equipment qualification
• Strong technical writing and documentation abilities
• Excellent communication and leadership skills

**Weil Group is proud to be an Equal Employment Opportunity Employer.**