Role Summary
We are seeking an experienced Commissioning and Qualification (C&Q) professional to lead our CQV Area team. As a seasoned manager, you will oversee the commissioning and qualification of high-profile pharmaceutical projects.
Your primary responsibility will be to manage a team of C&Q engineers on client sites throughout the project lifecycle. You will ensure that all activities are carried out in compliance with company guidelines, department procedures, and safety standards.
Key Responsibilities:
* Manage a team of C&Q engineers on high-profile client sites throughout the project lifecycle.
* Evaluate technical documentation from early design phases to guarantee alignment with GMP and CQV requirements.
* Analyze site issues through collaboration with Jacobs engineers or suppliers.
* Craft strategies for effective execution within tight timelines by identifying risks at initial stages.
* Delve into knowledge needed for critical processes such as mechanical completion procedure & construction scope
* Mentor junior staff members while fostering teamwork via discussions directly targeting optimal management principles aligned towards coordinated reporting streams eventually incorporating expert-level teaching skills ensuring seamless integration leading quality over standardization remaining forward-focused steering exactly authoritative judgement commitment true performers meeting given goal out,
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