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Lonza

Global life sciences contract manufacturer

Biotechnologist - Cell & Gene Therapy

Bioprocess & BiomanufacturingConfirmed live in the last 24 hours
Full-timeSingapore

About the Job

Requirements

  • A degree or equivalent qualification in Biotechnology, Biochemistry, Life Sciences, Engineering, or a related discipline is required.
  • Relevant academic, technical, or industry experience is required; biopharmaceutical manufacturing experience is advantageous but not essential.
  • Knowledge of biopharmaceutical processing, aseptic techniques, or cleanroom operations is advantageous.
  • A basic understanding of current Good Manufacturing Practice (cGMP), quality, safety, and data integrity principles is required.
  • Ability to learn and work with electronic manufacturing and quality systems is required.
  • Willingness to work in a cleanroom environment and on a rotating 12-hour shift pattern is required.

Responsibilities

  • Perform current Good Manufacturing Practice (cGMP) manufacturing activities using aseptic and cleanroom practices.
  • Complete batch records, logbooks, and Good Manufacturing Practice (GMP) documentation accurately and on time.
  • Perform environmental monitoring, equipment cleaning, sanitization, and production support activities.
  • Use electronic systems including DMS, LIMS, and TrackWise.
  • Review batch records and logbooks to support timely manufacturing operations.
  • Identify and escalate deviations, equipment alarms, and other non-routine events.
  • Maintain training requirements and contribute to safety, quality, and continuous improvement initiatives.

Desired Qualifications

  • Biopharmaceutical manufacturing experience is advantageous but not essential.
  • Knowledge of biopharmaceutical processing, aseptic techniques, or cleanroom operations is advantageous.

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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