Senior Specialist, QA (Lot Review)
Lonza is hiring a Senior QA Specialist in Singapore to provide quality oversight for a large-scale biopharmaceutical contract manufacturing facility. The role involves reviewing batch records, SOPs, and reports while ensuring adherence to GMP and regulatory standards. Candidates must have experience in biopharma QA operations and strong knowledge of regulatory guidelines like FDA, EMA, and ICH. The position offers career growth opportunities within a global life sciences company.
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Experience
Experience not specified
Function
Quality Assurance
Work mode
Onsite, Singapore
Company
Tier 2
What you will work on
Lonza is hiring a Senior QA Specialist in Singapore to provide quality oversight for a large-scale biopharmaceutical contract manufacturing facility. The role involves reviewing batch records, SOPs, and reports while ensuring adherence to GMP and regulatory standards. Candidates must have experience in biopharma QA operations and strong knowledge of regulatory guidelines like FDA, EMA, and ICH. The position offers career growth opportunities within a global life sciences company.
TAL's take
Lonza is a reputable global leader in biopharma manufacturing offering a clear, stable scope for an experienced QA professional.
The JD is highly specific to biopharmaceutical manufacturing, listing clear regulatory and operational requirements for a niche QA role.
Must haves
- Bachelor’s degree with experience in biopharmaceutical Quality Assurance
- Experience in QA operations in a GMP-regulated biopharma environment
- Understanding of quality management systems and GMP compliance
- Familiarity with FDA, EMA, and ICH regulatory guidelines
- Experience collaborating with cross-functional manufacturing teams
Tools and skills
About the company
Lonza is a well-established global life sciences contract manufacturer, classified as a large, respected industry player rather than a high-growth software unicorn.
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