LonzaSenior Specialist, QA (External)
Lonza is hiring a Senior Specialist, QA (External) in Singapore, Singapore. Level rates it ; you can apply on Lonza.
Level's read on this job
- On Level's scale, this role is Little AI ●○○○: aI is not part of the work.
- Tools and skills the posting cites include Sop, quality assurance and gmp.
- Level classifies it as a senior role.
- Level lists 580 other open roles at Lonza.
AI in this role
Support daily QA activities, deviation investigations, and regulatory compliance within a biopharmaceutical manufacturing facility.
The QA Specialist will support day-to-day Quality Assurance activities.
Find out more about what a life at Lonza in Singapore could look like for you by watching this short video.
This is a fully site‑based role. Working together in person supports close, real‑time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards.
What you’ll get
- An agile career and dynamic working culture in a global life sciences leader.
- An inclusive and ethical workplace that values diversity and integrity.
- Competitive compensation programs that recognize high performance.
- Professional growth opportunities through cross-functional projects and global exposure.
- Comprehensive medical insurance, with the option to enroll family members at partially subsidized premiums.
- Company transport provided from designated MRT locations to and from the Tuas site.
- Access to Lonza’s full suite of employee benefits: www.lonza.com/careers/benefits
What you will do:
- Support daily QA activities in compliance with approved SOPs, policies, and cGxP requirements.
- Review and approve SOPs, protocols, reports, and quality records.
- Lead deviation investigations, change controls, CAPA plans, and troubleshooting activities.
- Ensure data integrity and drive continuous quality improvement.
- Support and lead regulatory inspections, customer audits, and audit responses.
- Perform material release, qualification, defect inspections, and review vendor investigation reports.
- Lead projects, manage deliverables, and coordinate cross-functional activities.
- Maintain strong stakeholder relationships and develop training and internal GxP auditing competencies.
- Participate in facility walkdowns and perform other duties as assigned.
What we are looking for:
- Degree or higher from recognized institution with 3 to 10 years’ experience in Validation / Quality unit in the Biopharmaceutical industry
- Familiar with Regulatory requirements and local Codes & Standards (e.g., FDA, EMEA, and ICHQ7).
- Good knowledge and experience of the practical and theoretical requirement of quality management system in a GMP facility
- Team player who can operate independently, with strong focus on safety, quality and timelines
About Lonza
At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of.
Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment for all employees. If you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board.
Ready to shape the future of life sciences? Apply now.
How we rate this
Senior Specialist, QA (External) at Lonza rates 0 out of 100 for how much of the daily work is AI. That makes it Little AI (AI Level 1 of 4). The level is about AI in the job, not seniority.
Little AI. AI is not part of the work.
- ●●●● Builds AI80 to 100
- ●●●○ Works on AI60 to 79
- ●●○○ Uses AI40 to 59
- ●○○○ Little AI0 to 39
Levels come from how often the tools, models and workflows of the role are named in the posting itself. Read the description and count the AI tools, models and workflows it names.
Prepare for this job
Built from this posting and from similar jobs on Level.
Skills and AI tools this role asks for
Questions you could be asked
- Tell me about a project where quality assurance was part of your work. What did you do?
- Tell me about a project where gmp was part of your work. What did you do?
- Tell me about a project where deviation investigation was part of your work. What did you do?
- Tell me about a project where capa was part of your work. What did you do?
- Tell me about a project where biopharmaceuticals was part of your work. What did you do?
Adapt your resume
- List these exact terms on your resume: Quality Assurance, Gmp, Deviation Investigation, Capa, and Biopharmaceuticals. An applicant tracking system matches the wording, not the idea.
- Attach one line of real, concrete experience to at least one of them. A tool named with nothing behind it rarely survives a human read.
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