Summary

The consultant will deliver technical support for Commissioning, Qualification, and Validation (CQV). The CQV consultant is accountable for all CQV-related activities. This includes providing an update on the status of each document. The validation service will serve as the primary means to ensure that the schedule remains on track. The validation consultant should notify the project manager of any risks that could impact on the project plan and should provide support during project meetings.

Location

Aguadilla, PR

Education

Bachelor’s degree in Engineering or a Scientific field.

Preferred Qualifications

• 5+ years of experience in a regulated industry.
• Strong knowledge of cGMP/FDA regulations.
• Ability to develop and adhere to self-directed standard work-organized and methodical with míni

Responsibilities

• Review CQV documents following standards and procedures.
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