Validation Engineer II

The Validation Engineer II ensures compliance and operational excellence by managing validation processes across sterile and non-sterile manufacturing, overseeing multiple projects, developing documentation, and collaborating with teams to enhance efficiency, support product development, and drive continuous improvement.

Requirements

• Bachelor of Science degree in a scientific or engineering discipline
• 7 years Validation experience in the pharmaceutical or biotechnology industries
• Advanced knowledge of cGMP, CQV, sterilization process validation, and regulatory compliance
• Strong problem-solving, project management, and attention to detail
• Proficiency in Microsoft Office Suite, Quality Management Systems, and experience in Computer System Validation and Cleaning Validation

Benefits

• Medical, dental and vision benefits
• 401(k) matching
• Paid vacation time
• Paid holidays
• Sick leave
• Health insurance