Analytical Development Scientist

ESCO ASTER PTE. LTD.; Singapore; On-site; SGD 55,000 - 90,000; Full time

Job summary

Esco Aster Pte Ltd is hiring for an Analytical Development role based at our Singapore facility. The successful candidate will perform routine analytical testing, execute assays, and contribute to method development to support drug substance and product characterization.

Join a growing CDMO team, with opportunities to collaborate with Process Development and Quality, and to participate in technology transfer within a dynamic startup-phase environment.

Qualifications

• Hands-on experience with basic cell culture, cell-based assays and ELISA.
• Experience with analytical techniques such as HPLC, UV-Vis spectrophotometry and Karl Fischer titration.
• Experience in flow cytometry, qPCR and Western blotting would be an advantage with on-the-job training.
• Understand and work according to GDP and cGxP requirements.
• Meticulous in scheduling experiments and documenting analytical reports.
• Ability to communicate results with internal stakeholders and plan next steps.
• Willingness to learn new analytical techniques and deepen skills.
• Collaborate with cross-functional teams for tech transfer of analytics to operations.
• Perform tasks per regulations and site safety requirements.
• Undertake other tasks as assigned.

Responsibilities

• Perform routine analytical testing and assay execution.
• Develop and transfer analytical methods.
• Collaborate with Process Development and Quality teams on programs.
• Support investigations and project deliverables.

Skills

Cell culture

Cell-based assays

ELISA

HPLC

UV-Vis spectrophotometry

Karl Fischer titration

Flow cytometry

qPCR

Western blot

Education

Bachelor's degree in Life Sciences

Tools

Microsoft Excel

JMP

Prism

Job description

Esco Aster Pte Ltd is hiring for an Analytical Development role based at our Singapore facility. The successful candidate will perform routine analytical testing, execute assays, and contribute to method development to support drug substance and product characterization.

Join a growing CDMO team, with opportunities to collaborate with Process Development and Quality, and to participate in technology transfer within a dynamic startup-phase environment.