Specialist 3, QA Operations (Lot Release)

Lonza; Singapore; On-site; SGD 60,000 - 80,000; Full time

Job summary

A leading global biotechnology company in Singapore is seeking a Quality Assurance professional to oversee day-to-day operations at a GMP facility. You will ensure compliance by reviewing and approving various documents and lead quality control initiatives. The ideal candidate holds a Bachelor's degree in a related field, has over 5 years of QA experience, and is well-versed in regulatory guidelines. This role offers an inclusive corporate culture, competitive compensation, and extensive benefits.

Benefits

Compensation that recognizes high performance

Daily company bus from MRT

Fully paid medical insurance

Qualifications

• 5+ years of QA experience in GMP biopharma or similar regulated environment.
• Working knowledge of FDA, EMA, and ICH Q7 guidelines.
• Proven experience with deviations, CAPAs, and change control.

Responsibilities

• Perform day-to-day QA oversight in a multi-product GMP facility.
• Review and approve SOPs, protocols, reports, batch records and batch disposition.
• Lead or participate in deviations, change controls, and CAPAs.

Skills

Quality Assurance oversight

Risk-based decision-making

Strong communication

Collaboration across functions

Organizational skills

Education

Bachelor’s degree in Chemical, Biomedical, or related Engineering

Job description

Join Lonza in Singapore and help ensure safe, compliant lot release for therapies that change lives. You’ll provide QA oversight, solve problems, and drive continuous improvement in our GMP facility.

What you will get

• An agile career and dynamic working culture.
• An inclusive and ethical workplace.
• Compensation programs that recognize high performance.
• Daily company bus from the MRT location near your home to and from the Tuas site.
• Fully paid medical insurance, and option to enroll family members at partially subsidized premiums.
• Our full list of global benefits can be found here: https://www.lonza.com/careers/benefits.

What you will do

• Perform day-to-day QA oversight in a multi-product GMP facility.
• Review and approve SOPs, protocols, reports, batch records and batch disposition.
• Lead or participate in deviations, change controls, and CAPAs.
• Troubleshoot quality issues using risk-based decision-making.
• Build strong partnerships with manufacturing, QC, and support teams.
• Plan and coordinate cross-functional activities to meet timelines.
• Uphold data integrity; identify and implement process improvements.

What we are looking for

• Bachelor’s degree in Chemical, Biomedical, or related Engineering.
• 5+ years’ QA experience in GMP biopharma or similar regulated environment.
• Working knowledge of FDA, EMA, and ICH Q7 guidelines.
• Proven experience with deviations, CAPAs, and change control.
• Strong written and verbal communication; collaborate across functions.
• Organized, meticulous, and systematic; prioritize safety, quality, and timelines.
• Ability to lead small projects and train others in area of expertise.

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.