Purification Development Lead Scientist

Lonza Group Ltd.

Singapore

On-site

Confidential

Full time

5 days ago
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Benefits offered by this job

Medical insurance
Transport to Tuas
Global exposure
Career growth
Benefits package

Job summary

Lonza Singapore is seeking a Lead Scientist, Purification Development to drive downstream process development for therapeutic proteins. You will oversee chromatography, UF/DF, and viral clearance activities, plan studies, and ensure high-quality data for regulatory submissions.

You will train junior scientists, interpret study outcomes, and provide technical support for manufacturing operations. This role offers growth in a global life sciences leader with diverse project exposure.

Qualifications

  • Degree or PhD in Life Sciences or related field with industry experience.
  • 4–7 years' experience in protein purification and process development; PhD candidates with 2–5 years also considered.
  • Strong knowledge of purification techniques and Process Characterization.
  • Familiarity with cGMP/BLA requirements preferred.

Responsibilities

  • Lead process development and characterization activities, including study planning and interpretation.
  • Conduct DoE, risk assessments, scale-down studies, and support regulatory submissions.
  • Oversee purification activities using chromatography and UF/DF techniques.
  • Train and mentor junior scientists and ensure timely project delivery.
  • Prepare protocols, reports, SOPs, and technical documentation.
  • Provide support for manufacturing operations and tech transfer.
  • Coordinate internal/external communications and project coordination.

Skills

Protein purification
Process characterization
DoE data analysis
Strong communication
Team collaboration

Education

PhD in Life Sciences or related field
4–7 years protein purification experience

Tools

ÄKTA/UNICORN
JMP

Job description

Lonza Singapore is seeking a Lead Scientist, Purification Development to drive downstream process development for therapeutic proteins. You will oversee chromatography, UF/DF, and viral clearance activities, plan studies, and ensure high-quality data for regulatory submissions.

You will train junior scientists, interpret study outcomes, and provide technical support for manufacturing operations. This role offers growth in a global life sciences leader with diverse project exposure.

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