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Quality Validation Specialist - Singapore - GMP TECHNOLOGIES (S) PTE LTD
Description
Roles & ResponsibilitiesQuality Validation Specialist (1-year Contract)
Our client is a global pharmaceutical company aim to improve the quality of human life. The company is one of the leading MNCs in developing and manufacturing drugs, vaccines, and consumer healthcare products.
Responsibilities:
Requirements:
To apply, please visit and search for Job Reference #: 24330.
To find out more about this opportunity, please contact Patricia Lin @
We regret that only shortlisted candidates will be notified.
GMP Technologies (S) Pte Ltd | EA Licence: 11C3793 | EA Personnel: Patricia Lin | Registration No: R
Tell employers what skills you havePharmaceutical Industry
CAPA
Quality Assurance
Quality System
Healthcare
GMP
Investigation
Chemistry
Compliance
Equipment Qualification
Audits
Change Control
Regulatory Requirements
Manufacturing
