Document QA Engineer
The Document QA Engineer at Wuxi Apptec is responsible for maintaining GMP documentation, training records, and document control systems in a pharmaceutical factory setting. Core tasks include managing SOPs, digitizing records, and supporting internal/external audits. The role requires proficiency in Microsoft Office and specific quality systems like Veeva and TrackWise. Candidates should have a background in pharmacy or chemistry and strong compliance knowledge.
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Experience
0-1 years
Function
Quality Assurance
Work mode
Onsite, Singapore
Company
Tier 2
What you will work on
The Document QA Engineer at Wuxi Apptec is responsible for maintaining GMP documentation, training records, and document control systems in a pharmaceutical factory setting. Core tasks include managing SOPs, digitizing records, and supporting internal/external audits. The role requires proficiency in Microsoft Office and specific quality systems like Veeva and TrackWise. Candidates should have a background in pharmacy or chemistry and strong compliance knowledge.
TAL's take
Solid role at a well-known life sciences company with clear domain-specific documentation responsibilities.
The JD provides a highly detailed list of responsibilities and required systems, leaving no ambiguity about the daily tasks.
Must haves
- College diploma or above
- Proficiency in Microsoft Office
- Knowledge of GMP regulations
- Proficiency in written and spoken Chinese and English
Tools and skills
About the company
Global CRO with established reputation in life sciences and pharmaceuticals.