(Senior) Quality Specialist

Esco Lifesciences Group is Singapore’s most globalised life sciences company, with annual revenues close to SGD 200M and global operations in over 42 locations and 26 direct countries across North America, Europe, Asia, Oceania.

Esco Aster Pte Ltd is an affiliate of Esco Lifesciences Group and was first incorporated in 2017. It is a contract research, development and manufacturing organisation founded and deeply rooted by scientists, enabling fellow scientists to translate their bench work into commercially available products at affordable prices.

Our scientific work is in emerging and frontier biology utilizing cells as a final product or deriving products from cells which are often used as the factory to produce our target product. We are the first in the region to operate a full end‑to‑end integrated cell line creation / immortalisation or engineered cell line, cell culture process development, analytical development for stem cells and exosomes with full cGMP capabilities from drug substance and small‑scale fill & finish for final cell‑therapy product.

The work we do creates a remarkable and lasting impact on our world. We offer you an opportunity to be part of this exciting journey to own your career and gain firsthand exposure to new emerging modalities supporting translational sciences.

Join us as we redefine biosolutions for one world and one health for the current and future generations.

Who we’re looking for

• Strong leadership and communication skills.
• Ability to stay focused under pressure and adapt proactively.
• Critical thinker with a systematic and meticulous approach.
• Curious and self‑motivated to stay updated on cell‑gene therapy and emerging technologies.
• Committed to safety, quality, compliance, and timely delivery.
• Experience in cleanroom and GMP manufacturing settings.
• Required to wear full gowning / PPE.
• May engage in overtime during campaign activities or urgent troubleshooting.

The Scope

To support Quality functions from GMP readiness to ongoing compliance for cell and gene therapy manufacturing in a cGMP environment, ensuring adherence to global regulatory standards through oversight of operations, documentation, and quality systems.

Primary work location : Ayer Rajah Crescent, Singapore

Job Responsibilities

Requirements

Apply now by submitting a Cover Letter and CV to .

Seniority level

Associate

Employment type

Full‑time

Job function

Quality Assurance

#J-18808-Ljbffr