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C&Q Specialist

Puerto Rico, PR · Biotech/Pharmaceutical
Looking for a person understanding of all systems and processes included in the C&Q project scope.

Commissioning & Qualification resources are required for this project. The resources must meet the following requirements:
    Tested skills developing Decommissioning reports.
    Hands-on experience in document control & archiving programs.
    Minimum seven (7) to ten (10) years of validation experience in a pharmaceutical environment. 
    Good interpersonal skills with an assertive and pro-active approach towards work.
    Excellent communication skills (English and Spanish).

As a team member, a group leader (Senior) must integrate to achieve the following activities:
    Responsible and accountable of the coordination and performance of the consultant’s team.
    Manage distribution hours of project.
    Accomplish and/or update the timeline of project schedule.
    Manage the meetings with Client owners and C&Q project leader.
    Minimum seven (7) to eight (10) years of validation experience in a pharmaceutical environment. 

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

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