The CQV Consultant will document and review CQV processes, ensure compliance, lead validation efforts, and assist in issue resolutions in biopharmaceutical manufacturing settings.

The role involves repairing and maintaining production machinery, coordinating with supervisors for maintenance schedules, documenting work in a CMMS program, and ensuring a safe work environment, while performing tasks on rotating shifts.

The Process Engineer resolves technical equipment issues, optimizes processes, prepares documentation for inspections, and supports system changes in pharmaceutical manufacturing.