CQV Area Lead Job
Join us as a skilled CQV professional to lead high-profile client projects throughout their lifecycle.
This role requires expertise in commissioning and qualification activities for pharmaceutical facilities, with strong leadership skills to manage teams of engineers.
We are seeking an experienced individual who can identify the appropriate commissioning and qualification strategy for each project, define the required activities, and review technical documentation to ensure alignment with GMP requirements.
Key Responsibilities:
* Broad experience in validation master plans, commissioning master plans, project procedures & protocols (SAT/Commissioning) is essential. Strong design review process knowledge alongside GMP risk assessment will be utilized across multiple functions within this quality assurance role. Our ideal candidate must have been proficient working under cGMP guidelines while collaborating directly onsite from start-to-finish on various multi-phased drug processing facility developments worldwide. This job entails interaction at all levels including site engineering staff management which involves team leaders representing Jacobs engineers along together vendors following handover processes completion stages - predominantly remote office sites some hybrid.
* The successful candidate should ideally hold a degree or equivalent qualification relevant to an engineering discipline coupled by at least ten years’ previous involvement inside pharma sector operations; senior technical personnel might reasonably still secure themselves past entry-tier talent given stronger rapport build&
* A thorough understanding including methods integral towards fastidious representation – allowing improved efficiency supporting long-term endeavors driving opportunities forward nowadays.