The QC Analyst will be responsible for Biochemistry Area in the QC Lab to support Lot Release activities.
Requirements
- Degree or higher with ≥3 years of QC/Quality experience in biopharmaceuticals
- Preferably lab experience in biotech or medically related fields
- Familiarity with FDA, EMEA, ICH guidelines and GMP quality systems
- Strong planning, prioritization, and documentation skills
- Good communication and interpersonal abilities
- Analytical, meticulous, and quality-focused mindset
- Team player who can work independently with strong safety and timeline discipline
- Openness to new challenges and continuous improvement
Benefits
- 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