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Lonza

Global life sciences contract manufacturer

Analyst – Development Services - Analytical Development

Bioprocess & BiomanufacturingConfirmed live in the last 24 hours
Full-timeSingaporeNo salary listed

About the Job

Requirements

  • A degree in a relevant Science field or equivalent is required.
  • The role is suited to recent graduates and candidates with 1–2 years of laboratory experience.
  • A good understanding and application of current Good Manufacturing Practice (cGMP) concepts is an added advantage.

Responsibilities

  • Execute laboratory work supporting analytical testing on antibodies and other therapeutic recombinant proteins.
  • Under supervision, author method development and validation study protocols and reports, ensuring delivery of high-quality and cGMP-compliant data where applicable.
  • Use methods including capillary electrophoresis, high-performance liquid chromatography (HPLC) and ultra-performance liquid chromatography (UPLC), spectrophotometry, enzyme-linked immunosorbent assays (ELISAs), and quantitative polymerase chain reaction (qPCR).
  • Collaborate with different functional analytical teams by supporting analytical work for other teams where required.
  • Contribute to customer projects by generating scientific data from experimental work.
  • Work as part of site and global project teams to ensure timely delivery of project work stages.
  • Facilitate communication between other departments in Singapore, including quality control, quality assurance, supply chain management, and environmental, health, and safety.

Desired Qualifications

  • Practical laboratory experience in analytical testing for antibodies or other recombinant proteins is advantageous, although training will be provided.
  • Analysis of recombinant proteins is an added advantage.

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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