Be Part of a Leading Biologics Manufacturing Environment!
Are you an experienced QC professional with a strong background in GMP and equipment qualification? Here’s an opportunity to take on a pivotal role in supporting laboratory compliance, equipment qualification, and quality excellence within a global biopharmaceutical manufacturing environment!
Key Responsibilities
- Develop, review and execute qualification protocols for QC laboratory equipment to ensure compliance with GMP requirements.
- Support equipment qualification activities, including testing, documentation and verification of qualification results.
- Perform control trending and critical material qualification activities to maintain laboratory quality standards.
- Provide QC system administration support and work with laboratory systems such as LabWare and MODA.
- Ensure equipment qualification activities align with applicable regulatory requirements and internal quality procedures.
- Coordinate qualification projects, track progress and ensure timely completion of deliverables.
- Maintain accurate documentation and collaborate with cross-functional teams to support inspection readiness and operational excellence.
Requirements
- Relevant experience in the pharmaceutical industry, with a sound understanding of GMP requirements.
- Hands-on experience in QC equipment qualification, including writing qualification protocols, is essential.
- Experience with equipment such as TOC analysers and microplate readers will be an advantage.
- Familiarity with control trending, critical material qualification, LabWare and MODA.
- Experience in QC system administration and basic knowledge of regulatory requirements for equipment qualification.
- Strong project management, documentation and communication skills.
Interested candidates, please submit your CV to *************
Leon Leong De Cong
CEI Reg. No.: R1551708
Recruit Express Pte Ltd
EA Licence No.: 99C4599