About this role
Looking for a person understanding of all systems and processes included in the C&Q project scope.
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.
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 consultants 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.*