About this role
Provide oversight for day-to-day Quality Assurance activities and ensure compliance with SOPs and cGxP requirements in a biotech contract manufacturing facility. Lead complex special projects and provide strategic guidance on quality operations and compliance to senior management.
Requires a diploma or degree in Engineering or Science with 1-4 years of experience in the pharmaceutical manufacturing industry. Must possess excellent knowledge of regulatory requirements and adherence to industry codes and standards.
What they're looking for
Quality AssurancecGxP ComplianceGDP CorrectionsProblem SolvingData AnalysisQuality SystemsQuality OperationsProject Management
Frequently asked questions
What does a Specialist, Quality Assurance (Master Batch Record) at Lonza do?
Provide oversight for day-to-day Quality Assurance activities and ensure compliance with SOPs and cGxP requirements in a biotech contract manufacturing facility. Lead complex special projects and provide strategic guidance on quality operations and compliance to senior management. Requires a diploma…
What skills does this Specialist, Quality Assurance (Master Batch Record) role need?
Key skills for this role include Quality Assurance, cGxP Compliance, GDP Corrections, Problem Solving, Data Analysis, Quality Systems.
How much does a Specialist, Quality Assurance (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, Quality Assurance (Master Batch Record) role remote, hybrid, or on-site?
This role is on-site, based in Singapore.
How do I apply for this Specialist, Quality Assurance (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.