About this role
Oversee daily Quality Assurance activities in a multi-product cGxP manufacturing environment to ensure compliance with GMP and company standards. Lead deviation investigations, approve quality documentation, and provide QA oversight for manufacturing operations and regulatory inspections.
Requires a Bachelor's degree and proven experience in QA operations within a GMP-regulated biopharmaceutical environment. Candidates must have a solid understanding of FDA, EMA, and ICH guidelines and the ability to work a rotating 12-hour shift.
What they're looking for
Quality AssurancecGMP ComplianceBatch Record ReviewDeviation InvestigationCAPA ImplementationRoot Cause AnalysisChange ControlData Integrity
Frequently asked questions
What does a Lead Specialist, QA (CGT) at Lonza do?
Oversee daily Quality Assurance activities in a multi-product cGxP manufacturing environment to ensure compliance with GMP and company standards. Lead deviation investigations, approve quality documentation, and provide QA oversight for manufacturing operations and regulatory inspections. Requires a…
What skills does this Lead Specialist, QA (CGT) role need?
Key skills for this role include Quality Assurance, cGMP Compliance, Batch Record Review, Deviation Investigation, CAPA Implementation, Root Cause Analysis.
How much does a Lead Specialist, QA (CGT) at Lonza pay?
The employer did not list a salary for this role. Most similar Singapore roles publish their band on the job page.
Is this Lead Specialist, QA (CGT) role remote, hybrid, or on-site?
This role is on-site, based in Singapore.
How do I apply for this Lead Specialist, QA (CGT) role?
You can apply directly on Lonza's careers page. ApplyLah can tailor your résumé and cover letter to this exact role in seconds first.