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Zhejiang, China
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competitive rate
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pweatherby@leap29.com

Lead Commissioning & Qualification Engineers Required ¨C China ¨C Pharma / Biopharma

Location:        Zhejiang, China
Duration:        6 - 12 Month + Possible extension   
Working Week:  45 Hours / Week (Minimum) Expect 50 Hour + Weeks
Start Date:        Jan / Feb 2017
The Offer:        Market competitive rate + Accommodation + Flights for Mobilization if necessary  

The Company

An international engineering consultancy focusing on the pharmaceutical and biopharma industry. This company has offices throughout the USA, Europe and Asia employing over 200 staff worldwide.

The Project:

A Greenfield pharmaceutical and Biopharma production site.

The Jobs:

Lead C&Q Engineer ¨C Upstream

The function will be to walkdown, review construction package and execute commissioning and qualification of the following systems:

• Seed Bioreactors
• Production Bioreactors
• Wave Bioreactors

Lead C+Q Engineer ¨C Downstream

The function will be to walkdown, review construction package and execute commissioning and qualification of the following systems:

•        Centrifuge
•        Chromatography Columns and skids
•        Ultrafiltration Skids
•        Product holding tanks:
•        Temperature control units, portable glycol chiller
•        Slurry Loading Skid
•        Flow Packing Skid
Lead C+Q Engineer ¨C Utilities

The function will be to plan, supervise and manage all works associated with walkdown, commissioning and qualification of the following systems:

•        BMS Control
•        Fire Protection
•        ACMV (HVAC) and Booths/ BSC/ Cabinets
•        Black Utilities
•        Clean rooms/ Architectural finishes
•        Electrical systems






Job Requirements:

•        Degree Qualified in a relevant discipline
•        Experience gained within the above functions within a senior or lead capacity
•        Experience gained working on a pharmaceutical / biotechnology or biopharmaceutical project
•        Considerable experience gained within the commissioning and qualification stages of pharmaceutical / biotech or biopharmaceutical projects
•        Familiar with working to international standards
•        Can perform in a lead capacity with full autonomy (Zero Supervision)
•        Available to start a new role from Jan / February 2017 Onwards
•        Fluent written and spoken English & Mandarin
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