Job Opportunity
Job Description:
* Plan and lead a team of engineers in commissioning and qualifying CIP systems.
* Coordinate the completion of hydraulic balancing of CIP systems.
* Liaise with other system owners to ensure timely CIP testing.
* Participate in design document reviews to ensure quality aspects are included.
* Attend FAT and execute agreed testing protocols.
* Generate CQV documents at project level and for specific equipment/systems.
* Work with automation teams to ensure process descriptions are provided and functional specs are reviewed.
* Track and confirm closure of action items identified through FAT, HAZOP, Design Qualification, and other reviews.
* Maintain a strong interface with automation and engineering teams.
* Participate in construction system completion walkdowns.
* Lead a team of shift C&Q engineers in commissioning, cycle development, and shakedown activities.
* Perform shakedown and commissioning of systems.
* Introduce caustic to CIP skids and oversee safe use of caustic in cleaning cycle development.
* Oversee cycle development of cleaning cycles to reduce caustic concentration.
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Required Skills and Qualifications:
* B.Sc/B.Eng degree in an engineering discipline, particularly mechanical or process engineering.
* Extensive experience from biotechnology or pharmaceutical GMP manufacturing/CQV environment.
* Experience in commissioning and qualifying CIP systems.
* Leadership experience in managing teams of engineers.
* Demonstrated ability to work independently and respond proactively to business needs.
* Excellent interpersonal and communication skills.
* Familiarity with Delta-V & Navis Works is advantageous.
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About This Role:
This is a challenging opportunity to join our organization as a key member of our team.