About this role
The QA Specialist will support daily quality assurance activities in a GMP biotech manufacturing facility, including batch record reviews and deviation investigations. They will also oversee product release, manage quality documentation, and conduct shop floor walk-downs to ensure compliance.
Candidates must hold a degree and possess 2-5 years of experience in a similar industry or role. Strong knowledge of GMP, regulatory requirements, and quality management systems is essential.
What they're looking for
Quality AssuranceGMPBatch record reviewDeviation investigationRCACAPAChange controlRegulatory compliance
Frequently asked questions
What does a Specialist, QA Operations (Master Batch Record) at Lonza do?
The QA Specialist will support daily quality assurance activities in a GMP biotech manufacturing facility, including batch record reviews and deviation investigations. They will also oversee product release, manage quality documentation, and conduct shop floor walk-downs to ensure compliance. Candid…
What skills does this Specialist, QA Operations (Master Batch Record) role need?
Key skills for this role include Quality Assurance, GMP, Batch record review, Deviation investigation, RCA, CAPA.
How much does a Specialist, QA Operations (Master Batch Record) 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 Specialist, QA Operations (Master Batch Record) role remote, hybrid, or on-site?
This role is on-site, based in Singapore.
How do I apply for this Specialist, QA Operations (Master Batch Record) 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.