Job Description

Key capabilities include:

Demonstrates deep knowledge and expertise in design and implementation of engineering projects.

• Definition of functional, technical and quality requirements: process descriptions, equipment and control modules according to process and CIP/SIP recipes, functional specifications.
• Realization of reviews of process studies, P&IDs
• Review tender packages and oversight contractor\'s performance.
• Integration of operability and EHS requirements at all design steps.
• Preparation of the project testing, commissioning and inspection requirements
• Assessment of systems\' legal conformity.
• On-site verification of execution according to good practices
• Interface with Site existing / new utilities infrastructures, ensure fluids\' connections Soft Skills
• Team working & Communication / Autonomy / Contractors\' management.
• Good project integration experience: organization, cost, time, schedule, contracting, procurement, qualification, validation, technologies.
• Experience in the Bio-Pharmaceutical industry
• Perform his/her work in an EHS and cGMP high-demanding environment.

Overview

-Review documents for ITT process & contractors\' selection

-Detailed design studies review with contractors, including follow up of yellow reviews, functional specifications, piping and vessel design, 3D-model

-Works supervision, Walkdowns performed, FAT, SAT, IQ, OQ + punch list follow-up

-Provisional and final acceptances

- Final handover for process packages and systems

Qualifications:

• Chemical or Process engineering degree is required.
• +10 years\' experience in the field of Process engineering for capital investments is required, ranging from early design to facility start-up.
• Deep knowledge of commissioning and qualification of similar production trains is a must.
• Experience with Centrifugation and Ultrafiltration systems is a must.

Soft Skills

• Team working & Communication / Autonomy / Contractors\' management.
• Good project integration experience: organization, cost, time, schedule, contracting, procurement, qualification, validation, technologies.
• Experience in the Bio-Pharmaceutical industry
• Perform his/her work in an EHS and cGMP high-demanding Environment.
• Microsoft Office Suite Microsoft Visio Microsoft Project (preferred)
• SchedulePro/SuperPro or equivalent (preferred)

Language Proficiency

• English - Fluent Mandarin,
• French or German is a plus

No deviation