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Lonza

Global life sciences contract manufacturer

Process Engineer - Process

Bioprocess & BiomanufacturingConfirmed live in the last 24 hours
Full-timeTuas, SingaporeNo salary listed

About the Job

Requirements

  • A degree in an Engineering discipline, or a Diploma with Process Engineering experience.
  • Relevant experience operating and maintaining manufacturing equipment, preferably in biopharmaceutical or petrochemical facilities.
  • A good understanding of process equipment design and operation.
  • Strong problem-solving, troubleshooting, and analytical skills.
  • Strong written and oral communication skills.

Responsibilities

  • Provide operational and process support for manufacturing systems used to manufacture biologics products, including bioreactors, purification equipment, media and buffer systems, heat and cooling systems, and CIP/SIP equipment.
  • Develop and implement best practices to improve manufacturing success rates, maintain compliance, support a safe work environment, and control manufacturing operating costs.
  • Provide daily operational support and maintenance for biologics manufacture in a cGMP environment, including process and equipment modifications and changes, process troubleshooting, root cause analysis, and deviation investigation.
  • Participate in and lead investigations relating to audits and manufacturing processes, including contamination, observations, deviations, and discrepancies, and propose corrective and preventive actions.
  • Propose and evaluate equipment, process, and operational modifications to improve safety, increase efficiency, and support company goals.
  • Coordinate and manage project commissioning, IQ, and OQ phases; ensure completed projects, documents, and drawings are handed over to users and Maintenance; and complete project closeout.
  • Supervise outside contractors developing and implementing capital projects and plant modifications.
  • Participate in new-customer technology transfers and risk assessments as the process subject matter expert, and develop, plan, and execute work to ensure successful transfers.
  • Perform technical reviews as a process subject matter expert during revisions of GMP-controlled documents, including standard operating procedures, batch records, and commissioning or qualification protocols.
  • Use change control, permit-to-work processes, drawing management, and documentation in day-to-day activities.
  • Support the team during audits and inspections.

Desired Qualifications

  • Experience operating and maintaining manufacturing equipment in biopharmaceutical or petrochemical facilities.

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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