About this role
Provide quality oversight for engineering and validation activities, including the review and approval of validation master plans and protocols. Ensure strict adherence to cGMP requirements and manage the closure of deviations and CAPAs.
Requires a degree in Biological Science or Engineering with 5-8 years of experience in a validation or quality unit within the biopharmaceutical industry. Must possess strong knowledge of quality management systems in a GMP facility and the ability to work independently.
What they're looking for
Quality AssuranceProcess ValidationcGMP ComplianceValidation Master Plan ReviewRoot Cause AnalysisCAPA ManagementContinued Process VerificationRegulatory Standards
Frequently asked questions
What does a Senior Specialist, Quality Assurance (Process Support) at Lonza do?
Provide quality oversight for engineering and validation activities, including the review and approval of validation master plans and protocols. Ensure strict adherence to cGMP requirements and manage the closure of deviations and CAPAs. Requires a degree in Biological Science or Engineering with 5-…
What skills does this Senior Specialist, Quality Assurance (Process Support) role need?
Key skills for this role include Quality Assurance, Process Validation, cGMP Compliance, Validation Master Plan Review, Root Cause Analysis, CAPA Management.
How much does a Senior Specialist, Quality Assurance (Process Support) 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, Quality Assurance (Process Support) role remote, hybrid, or on-site?
This role is on-site, based in Singapore.
How do I apply for this Senior Specialist, Quality Assurance (Process Support) 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.