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Preferred qualifications include:
 •   Experience in GMP-regulated facilities.
•   Hands-on experience in commissioning, qualification, validation, and/or maintenance programs.
•   Strong technical documentation and report-writing skills.
•   Familiarity with regulatory requirements and industry best practices.
•   Ability to work effectively in a multidisciplinary project environment.
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.Â
   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.Â
**Weil Group is proud to be an Equal Employment Opportunity Employer.*
C&Q Executer · Weil Group, Inc