Job Summary
The CIP Systems Lead will oversee the commissioning and qualification of Clean-In-Place systems, requiring extensive experience in biotechnology or pharmaceutical GMP manufacturing/CQV environments.
* Develop and execute plans for team members to commission and qualify CIP systems.
* Liaise with other teams to ensure testing schedules are met.
* Review design documents to ensure quality aspects are included.
Key Responsibilities:
* Plan and lead commissioning and qualification of CIP systems.
* Liaise and coordinate CIP testing activities.
* Participate in design reviews and ensure quality aspects are included.
* Attend Factory Acceptance Tests (FAT) and execute agreed testing protocols.
Requirements:
* Bachelor's degree in a relevant engineering discipline.
* Extensive experience from biotechnology or pharmaceutical GMP manufacturing/CQV environments.
* Proven ability to work independently and respond to business needs.
* Excellent communication and interpersonal skills.