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Lonza

Global life sciences contract manufacturer

Senior QC Analyst - Biochem

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeTuas, SingaporeNo salary listedIn-person

About the Job

Requirements

  • A degree or higher qualification in Biochemistry, Biotechnology, Life Sciences, Pharmaceutical Sciences, Chemistry, or a related discipline.
  • Zero to five years of Quality Control or laboratory experience within the biopharmaceutical, biotechnology, or pharmaceutical industry.
  • Hands-on experience with biochemical and analytical techniques such as ELISA, PCR, SDS-PAGE, IEF potency assays, and Biacore.
  • Experience supporting method transfers, method validations, equipment qualification, and laboratory investigations.
  • Good understanding of cGMP requirements, quality management systems, data integrity principles, and global regulatory expectations including FDA, EMA, and ICH guidelines.
  • Strong analytical, troubleshooting, problem-solving, and quality decision-making skills, with the ability to work independently and prioritize effectively.
  • Strong communication and interpersonal skills with a collaborative mindset and commitment to safety, quality, and operational excellence.

Responsibilities

  • Perform and prioritize testing of final product, in-process, and stability samples in accordance with approved test methods, SOPs, and cGMP requirements.
  • Execute biochemical and analytical methods including ELISA, PCR, SDS-PAGE, IEF potency assays, Biacore, and other physicochemical techniques.
  • Support method transfers, method validations, equipment qualification activities, and laboratory troubleshooting to ensure operational readiness and compliance.
  • Document, review, and maintain laboratory data and records in accordance with GMP requirements and data integrity principles.
  • Investigate laboratory events including OOS, deviations, and analytical issues, supporting root cause analysis and technical report generation.
  • Author and maintain quality documentation including Change Controls, SOPs, test methods, and laboratory procedures.
  • Contribute to continuous improvement initiatives, laboratory operations, equipment maintenance, reagent preparation, and technical training activities.

About the Company

Lonza

Global life sciences contract manufacturer

Lonza is a global provider of development and manufacturing services for the pharmaceutical, biotechnology, and nutrition sectors. It supports clients from early development through to commercial production, offering integrated processes such as process development, GMP manufacturing, formulation, fill-finish, and quality assurance to bring medicines and nutrition products to market. Lonza’s model is built on end-to-end CDMO capabilities, enabling companies to move from concept to scalable, compliant production with reliable supply chains. What sets Lonza apart is its long history and global footprint, combining decades of experience across chemistry, biology, and nutrition with a broad, end-to-end service network that supports projects from discovery to commercialization. The company aims to be a trusted, long-term partner in life sciences by helping customers efficiently develop and manufacture their products at scale while maintaining strict regulatory and quality standards.

Company size
10,001+
Company stage
IPO
Headquarters
Basel, Switzerland
Founded
1897

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