C+Q Engineer - Singapore
C+Q Engineer - Singapore
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Job Description
Job Description
Commissioning Qualification and Validation Engineer (CQV) Singapore (Biopharma Projects)
The Company: Multi-disciplined engineering consultancy within the life sciences sector
Location Singapore
Working Week 45 Hours per Week Predominately site based (Tuas)
Offer: Competitive Monthly Pay AWS
The Company
A global EPCM engineering service provider with a significant presence in Southeast Asia focusing on the life sciences sector.
This company has a proven track record of delivering some of the largest GMP style projects globally with strong capability relating to process mechanical and project management scopes of work.
The Role
This will be a hands on field based execution role with direct system ownership of designated systems and responsibility for achievement of the required project quality and schedule requirements for those systems.
This individual will be required to prepare and execute C&Q documentation. Ensure that C&Q schedule requirements are being met for their systems.
Investigate / trouble-shoot / resolve any non-conformances. Initiate and close deviation reports.
Knowledge of GMP is required.
The Requirements
Ideally a Process / Chemical Engineering background
Minimum of 5 years of relevant experience
5 years Commissioning and Qualification experience in pharmaceuticals or biologics.
Right to live and work in Singapore. (Candidates located in the South East Asian regional can be considered)
In-depth equipment commissioning and startup knowledge and experience with strong troubleshooting skills. Must have hands-on commissioning experience.
Knowledge of biopharma unit operations is required
Employment Type
Full-Time
