Not specified; competitive compensation programs r...
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5 years qc experience in biopharmaceuticals
Proficiency in elisa pcr ce sds-page assays
Knowledge of cgmp data integrity requirements
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Lonza Group is seeking a QC Analyst specializing in biochemistry to support lot release activities in their QC Lab in Tuas, Singapore. The ideal candidate should possess a degree with at least five years of experience in QC within biopharmaceuticals and be familiar with relevant regulatory guidelines.
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Job Summary
The QC Analyst will be responsible for Biochemistry Area in the QC Lab to support Lot Release activities.
Employees receive competitive compensation programs, comprehensive medical insurance, and company transport from designated MRT locations.
The role requires executing methods such as ELISA, PCR, CE, and SDS-PAGE while maintaining compliance with cGMP standards.
Matching Summary
Match Score: 75
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Lonza Group is seeking a QC Analyst specializing in biochemistry to support lot release activities in their QC Lab in Tuas, Singapore. The ideal candidate should possess a degree with at least five years of experience in QC within biopharmaceuticals and be familiar with relevant regulatory guidelines.
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Salary
Not specified; Competitive compensation programs recognized for high performance
Skills & Requirements
Must-have
5 years QC experience in biopharmaceuticals
Proficiency in ELISA PCR CE SDS-PAGE assays
Knowledge of cGMP data integrity requirements
Nice-to-have
Experience with FDA EMEA ICH guidelines
Ability to lead OOS and deviation investigations
Strong communication and interpersonal skills
Key Requirements
Degree or higher with 5 years of QC/Quality experience
Familiarity with FDA EMEA ICH guidelines and GMP quality systems
Lab experience in biotech or medically related fields preferred