About this role
Provide QA oversight for manufacturing activities in a GMP biopharmaceutical facility to ensure regulatory compliance. Responsibilities include reviewing batch records, leading deviation investigations, and managing CAPA processes.
Requires a Bachelor's degree and proven experience in QA operations within a GMP-regulated biopharmaceutical environment. Candidates must be familiar with FDA, EMA, and ICH regulatory guidelines.
What they're looking for
Quality AssuranceGMP ComplianceLot ReviewBatch Record ReviewDeviation InvestigationsCAPAChange ControlGxP Standards
Frequently asked questions
What does a Senior Specialist, QA (Lot Review) at Lonza do?
Provide QA oversight for manufacturing activities in a GMP biopharmaceutical facility to ensure regulatory compliance. Responsibilities include reviewing batch records, leading deviation investigations, and managing CAPA processes. Requires a Bachelor's degree and proven experience in QA operations …
What skills does this Senior Specialist, QA (Lot Review) role need?
Key skills for this role include Quality Assurance, GMP Compliance, Lot Review, Batch Record Review, Deviation Investigations, CAPA.
How much does a Senior Specialist, QA (Lot Review) 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 Senior Specialist, QA (Lot Review) role remote, hybrid, or on-site?
This role is on-site, based in Singapore.
How do I apply for this Senior Specialist, QA (Lot Review) 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.