Job Description & Requirements
Responsibilities:
* Review project drawings: process P&IDs, AF&IDs, SLDs, Schematics, etc.
* Identify and create assets for operational readiness implementation.
* Work with cross-discipline engineering teams.
* Generate, process, and close work orders for project implementation.
* Gather data and information from vendors.
* Create preventive maintenance, calibration, and certification plans for newly implemented assets.
* Be involved in the handover and closeout of systems as part of the project life cycle.
* Identify and create asset spare list.
* Vendor and subcontractor coordination and site walkdowns.
* Perform site walk-downs and coordinate with stakeholders.
* P&ID review and updating.
* Multi-discipline drawing review.
* Coordination of meetings.
* Adhere to client safety requirements and GMP/Gowning requirements.
* Draft and execute commissioning and qualification protocols.
Requirements:
* Possess at least a Degree in Engineering or Facility Management - preferably in Chemical, Mechanical, Facility, or Pharmaceutical Engineering.
* Experience in Maximo or a similar Computerized Maintenance Management System (CMMS) or Enterprise Asset Management system (EAM) software is a plus.
* Languages: English - fluent in speaking and writing.
* Experience: Basic Biotech or Pharmaceutical cGMP experience is required.
* Broad knowledge of engineering disciplines, commissioning, compliance, qualification, and quality aspects of biopharma or pharmaceutical manufacturing.
* Structured and organized individual.
* Ability to apply standard Project Management tools, controls, and best practices.
* Strong oral and written communication skills.
* Ability to foster collaboration and work effectively on cross-functional teams.
* Demonstrate time management and decision-making skills.
* Critical thinking and problem-solving skills.
* Takes initiative with minimal supervision.
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