C&Q Specialist

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.